Imide
In organic chemistry, an imide is a functional group consisting of two acyl groups bound to nitrogen. The compounds are structurally related to acid anhydrides, although imides are more resistant to hydrolysis. In terms of commercial applications, imides are best known as components of high-strength polymers, called Polyimide, polyimides. Inorganic imides are also known as solid state or gaseous compounds, and the imido group (=NH) can also act as a ligand. Examples Simple example is diacetamide with the formula , formally the diacetylated derivative of ammonia. Commonly encountered imides, however, are cyclic, being derived from dicarboxylic acids. A common example is succinimide derived from succinic acid and ammonia. The names of these cyclic imides reflect the parent acid. Many imides are derived from primary amines as opposed to ammonia. These are indicated by ''N''-substituent in the prefix. For example, N-ethylsuccinimide is derived from succinic acid and ethylamine. ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Polyimide
Polyimide (sometimes abbreviated PI) is a monomer containing imide groups belonging to the class of high-performance plastics. With their high heat-resistance, polyimides enjoy diverse applications in roles demanding rugged organic materials, such as high temperature fuel cells, displays, and various military roles. A classic polyimide is Kapton, which is produced by condensation of pyromellitic dianhydride and 4,4'-oxydianiline.Wright, Walter W. and Hallden-Abberton, Michael (2002) "Polyimides" in ''Ullmann's Encyclopedia of Industrial Chemistry'', Wiley-VCH, Weinheim. History The first polyimide was discovered in 1908 by Bogart and Renshaw. They found that 4-amino phthalic anhydride does not melt when heated but does release water upon the formation of a high molecular weight polyimide. The first semialiphatic polyimide was prepared by Edward and Robinson by melt fusion of diamines and tetra acids or diamines and diacids/diester. However, the first polyimide of significant co ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Imide Functional Group
In organic chemistry, an imide is a functional group consisting of two acyl groups bound to nitrogen. The compounds are structurally related to acid anhydrides, although imides are more resistant to hydrolysis. In terms of commercial applications, imides are best known as components of high-strength polymers, called polyimides. Inorganic imides are also known as solid state or gaseous compounds, and the imido group (=NH) can also act as a ligand. Examples Simple example is diacetamide with the formula , formally the diacetylated derivative of ammonia. Commonly encountered imides, however, are cyclic, being derived from dicarboxylic acids. A common example is succinimide derived from succinic acid and ammonia. The names of these cyclic imides reflect the parent acid. Many imides are derived from primary amines as opposed to ammonia. These are indicated by ''N''-substituent in the prefix. For example, N-ethylsuccinimide is derived from succinic acid and ethylamine. : Prope ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Inorganic Imide
The inorganic imide is an inorganic chemical compound containing *an anion with the chemical formula , in which nitrogen atom is covalently bonded to one hydrogen atom (as in lithium imide and calcium imide ). The other name of that anion is monohydrogen nitride. *functional groups with the chemical formulas or , in which nitrogen atom is also covalently bonded to one hydrogen atom, with two covalent single bonds or one covalent double bond from the nitrogen atom to other atoms, respectively (as in heptasulfur imide , sulfur diimide and nitroxyl ). Imide, Organic imides have the functional groups or as well. The imides are related to the inorganic amides, containing the anions, the nitrides, containing the anions and the nitridohydrides or nitride hydrides, containing both nitride and hydride anions. In addition to solid state imides, molecular imides are also known in dilute gases, where their spectrum can be studied. When covalently bound to a metal, an imide ligand p ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Maleimide
Maleimide is a chemical compound with the formula H2C2(CO)2NH (see diagram). This unsaturated imide is an important building block in organic synthesis. The name is a contraction of maleic acid and imide, the -C(O)NHC(O)- functional group. Maleimides are also a ''class'' of derivatives of the parent maleimide where the N''H'' group is replaced with alkyl or aryl groups such as a methyl or phenyl, respectively. The substituent can also be a small molecule (such as biotin, a fluorescent dye, an oligosaccharide, or a nucleic acid), a reactive group, or a synthetic polymer such as polyethylene glycol. Human hemoglobin chemically modified with maleimide-polyethylene glycol is a blood substitute called MP4. Reactions Many analogues of maleimide are prepared by treating maleic anhydride with amines followed by dehydration. A defining feature of the reactivity of maleimides is their susceptibility to additions across the double bond either by Michael additions or via Diels-Alder react ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Succinimide
Succinimide is an organic compound with the formula (CH2)2(CO)2NH. This white solid is used in a variety of organic syntheses, as well as in some industrial silver plating processes. The compound is classified as a cyclic imide. It may be prepared by thermal decomposition of ammonium succinate. Succinimides Succinimides refers to compounds that contain the succinimide group. These compounds have some notable uses. Several succinimides are used as anticonvulsant drugs, including ethosuximide, phensuximide, and methsuximide. Succinimides are also used to form covalent bonds between proteins or peptides and plastics, which is useful in a variety of assay techniques. See also * Succinic anhydride * N-Hydroxysuccinimide, ''N''-Hydroxysuccinimide * N-Bromosuccinimide, ''N''-Bromosuccinimide References {{Authority control Succinimides, ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Phthalimide
Phthalimide is the organic compound with the formula C6H4(CO)2NH. It is the imide derivative of phthalic anhydride. It is a Sublimation (phase transition), sublimable white solid that is slightly soluble in water but more so upon addition of base (chemistry), base. It is used as a precursor to other organic compounds as a masked source of ammonia. Uses :image:Folpet.png, 160px, Folpet, a phthalimide, is a commercial fungicide., left Phthalimide is used as a precursor to anthranilic acid, a precursor to azo dyes and saccharin. Alkyl phthalimides are useful precursors to amines in chemical synthesis, especially in peptide synthesis where they are used "to block both hydrogens and avoid racemization of the substrates". Alkyl halides can be converted to the N-alkylphthalimide: : C6H4(CO)2NH + RX + NaOH → C6H4(CO)2NR + NaX + H2O The amine is commonly liberated using hydrazine: : C6H4(CO)2NR + N2H4 → C6H4(CO)2N2H2 + RNH2 Dimethylamine can also be used. Som ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Succinimide
Succinimide is an organic compound with the formula (CH2)2(CO)2NH. This white solid is used in a variety of organic syntheses, as well as in some industrial silver plating processes. The compound is classified as a cyclic imide. It may be prepared by thermal decomposition of ammonium succinate. Succinimides Succinimides refers to compounds that contain the succinimide group. These compounds have some notable uses. Several succinimides are used as anticonvulsant drugs, including ethosuximide, phensuximide, and methsuximide. Succinimides are also used to form covalent bonds between proteins or peptides and plastics, which is useful in a variety of assay techniques. See also * Succinic anhydride * N-Hydroxysuccinimide, ''N''-Hydroxysuccinimide * N-Bromosuccinimide, ''N''-Bromosuccinimide References {{Authority control Succinimides, ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Cycloheximide
Cycloheximide is a naturally occurring fungicide produced by the bacterium '' Streptomyces griseus''. Cycloheximide exerts its effects by interfering with the translocation step in protein synthesis (movement of two tRNA molecules and mRNA in relation to the ribosome), thus blocking eukaryotic translational elongation. Cycloheximide is widely used in biomedical research to inhibit protein synthesis in eukaryotic cells studied ''in vitro'' (''i.e.'' outside of organisms). It is inexpensive and works rapidly. Its effects are rapidly reversed by simply removing it from the culture medium. Due to significant toxic side effects, including DNA damage, teratogenesis, and other reproductive effects (including birth defects and toxicity to sperm), cycloheximide is generally used only in ''in vitro'' research applications, and is not suitable for human use as a therapeutic compound. Although it has been used as a fungicide in agricultural applications, this application is now decreas ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Kapton
file:Kaptonpads.jpg, Kapton insulating pads for mounting electronic parts on a heat sink Kapton is a polyimide film used in flexible printed circuits (flexible electronics) and space blankets, which are used on spacecraft, satellites, and various space instruments. Invented by the DuPont (1802-2017), DuPont Corporation in the 1960s, Kapton remains stable across a wide range of temperatures, from . Kapton is used in electronics manufacturing and space applications, with x-ray equipment, and in 3D printing applications. Its favorable thermal properties and outgassing characteristics result in its regular use in Cryogenics, cryogenic applications and in high vacuum environments. History Kapton was invented by DuPont in the 1960s. Kapton remains manufactured by DuPont to this day. The name ''Kapton'' is a registered trademark of E. I. du Pont de Nemours and Company. Chemistry and variants Kapton synthesis is an example of the use of a wikt:dianhydride, dianhydride in step pol ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Glutarimide
Glutarimide, also known by its chemical name 2,6-piperidinedione, is the organic compound with the formula (CH2)3(CO)2NH. It is a white solid compound that forms upon dehydration of the amide of glutaric acid. Glutaramide is at the core of numerous medical drugs and substances, including lenalidomide (a medication used to treat anemia and multiple myeloma), cycloheximide (a potent inhibitor of protein synthesis), and fluoxetine (an SSRI Selective serotonin reuptake inhibitors (SSRIs) are a class of drugs that are typically used as antidepressants in the treatment of major depressive disorder, anxiety disorders, and other psychological conditions. SSRIs primarily work by ...); as well as the sedative/"tranquilizer" hypnotic drugs glutethimide (branded "Doriden" until 1993 (in the US) and 2006 (in Hungary) and aminoglutethimide. References {{organic-compound-stub ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Thalidomide
Thalidomide, sold under the brand names Contergan and Thalomid among others, is an oral administered medication used to treat a number of cancers (e.g., multiple myeloma), graft-versus-host disease, and many skin disorders (e.g., complications of leprosy such as skin lesions). Updated as required. Thalidomide has been used to treat conditions associated with HIV: aphthous ulcers, HIV-associated wasting syndrome, diarrhea, and Kaposi's sarcoma, but increases in HIV viral load have been reported. Common side effects include sleepiness, rash, and dizziness. Severe side effects include tumor lysis syndrome, blood clots, and peripheral neuropathy. Thalidomide is a known human teratogen and carries an extremely high risk of severe, life-threatening birth defects if administered or taken during pregnancy. It causes skeletal deformities such as Amelia (birth defect), amelia (absence of legs and/or arms), absence of bones, and phocomelia (malformation of the limbs). A single dose of t ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |