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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] |
N-Chlorosuccinimide
''N''-Chlorosuccinimide (NCS) is the organic compound with the formula C2H4(CO)2NCl. This white solid is used for chlorinations. It is also used as a mild oxidant. NCS is related to succinimide, but with N-Cl in place of N-H. The N–Cl bond is highly reactive, and NCS functions as a source of "Cl+". Synthesis and selected reactions NCS is produced from succinimide by treatment with sources, such as sodium hypochlorite (bleach), and tert-Butyl hypochlorite, t-butylhypochlorite, and even chlorine. Electron-rich arenes are readily monochlorinated by NCS. Aniline and mesitylene are converted to the respective chlorinated derivatives. Related reagents * N-Iodosuccinimide, ''N''-Iodosuccinimide (NIS), the iodine analog of ''N''-chlorosuccinimide. * N-Bromosuccinimide, ''N''-bromosuccinimide (NBS), the bromine analog of ''N''-chlorosuccinimide. * Other ''N''-chloro compounds that are commercially available include chloramine-T, trichloroisocyanuric acid ((OCNCl)3), 1,3-dichloro-5,5 ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
N-Bromosuccinimide
''N''-Bromosuccinimide or NBS is a chemical reagent used in radical substitution, electrophilic addition, and electrophilic substitution chemical reaction, reactions in organic chemistry. NBS can be a convenient source of Br•, the bromine radical. Preparation NBS is commercially available. It can also be synthesized in the laboratory. To do so, sodium hydroxide and bromine are added to an ice-water solution of succinimide. The NBS product precipitates and can be collected by filtration. Crude NBS gives better yield in the Wohl–Ziegler reaction. In other cases, impure NBS (slightly yellow in color) may give unreliable results. It can be purified by recrystallization from preheated (90 to 95 °C) water (10 g of NBS for 100 mL of water). Reactions Addition to alkenes NBS reacts with alkenes in aqueous solvents to give Halohydrin formation reaction, bromohydrins. The preferred conditions are the portionwise addition of NBS to a solution of the alkene in 50% aqueo ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
N-Hydroxysuccinimide
''N''-Hydroxysuccinimide (NHS) is an organic compound with the formula (CH2CO)2NOH. It is a white solid that is used as a reagent for preparing active esters in peptide synthesis. It can be synthesized by heating succinic anhydride with hydroxylamine or hydroxylamine hydrochloride. Activating reagent NHS is commonly found in organic chemistry or biochemistry where it is used as an activating reagent for carboxylic acids. Activated acids (carboxylates) can react with amines to form amides for example, whereas a normal carboxylic acid would just form a salt with an amine. Use A common way to synthesize an NHS-activated acid is to mix NHS with the desired carboxylic acid and a small amount of an organic base in an anhydrous solvent. A coupling reagent such as dicyclohexylcarbodiimide (DCC) or 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) is then added to form a highly reactive activated acid intermediate. NHS reacts to create a less labile activated acid. The group is us ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
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] |
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] |
Ethosuximide
Ethosuximide, sold under the brand name Zarontin among others, is a medication used to treat absence seizures. It may be used by itself or with other antiseizure medications such as valproic acid. Ethosuximide is taken by mouth. Ethosuximide is usually well tolerated. Common side effects include loss of appetite, abdominal pain, diarrhea, and feeling tired. Serious side effects include suicidal thoughts, low blood cell levels, and lupus erythematosus. It is unclear if it has adverse effects on the fetus during pregnancy. Ethosuximide is in the succinimide family of medications. Its mechanism of action is thought to be due to antagonism of the postsynaptic T-type voltage-gated calcium channel. Ethosuximide was approved for medical use in the United States in 1960. It is on the World Health Organization's List of Essential Medicines. Ethosuximide is available as a generic medication. , its availability was limited in many countries, with concerns about price fixing in the Un ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Anticonvulsant
Anticonvulsants (also known as antiepileptic drugs, antiseizure drugs, or anti-seizure medications (ASM)) are a diverse group of pharmacological agents used in the treatment of epileptic seizures. Anticonvulsants are also used in the treatment of bipolar disorder and borderline personality disorder, since many seem to act as mood stabilizers, and for the treatment of neuropathic pain. Anticonvulsants suppress the uncontrolled and excessive firing of neurons during seizures and in doing so can also prevent the spread of the seizure within the brain. Conventional antiepileptic drugs have diverse mechanisms of action but many block sodium channels or enhance γ-aminobutyric acid ( GABA) function. Several antiepileptic drugs have multiple or uncertain mechanisms of action. Next to voltage-gated sodium channels and components of the GABA system, their targets include GABAA receptors, the GABA transporter type 1, and GABA transaminase. Additional targets include voltage-gate ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Methsuximide
Mesuximide (or methsuximide, methosuximide) is a succinimide anticonvulsant medication. It is sold as a racemate by Pfizer under the tradenames Petinutin (Switzerland) and Celontin (United States). The therapeutic efficacy of methosuximide is largely due to its pharmacologically active metabolite, ''N''-desmethylmethosuximide, which has a longer half-life and attains much higher plasma levels than its parent. Medical use is indicated for the control of absence seizure Absence seizures are one of several kinds of generalized seizures. Absence seizures are characterized by a brief loss and return of consciousness, generally not followed by a period of lethargy (i.e. without a notable postictal state). Absence ...s that are refractory to other drugs. References Anticonvulsants Drugs developed by Pfizer Succinimides {{anticonvulsant-stub ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Phensuximide
Phensuximide is an anticonvulsant in the 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 ... class. External links * * Succinimides {{anticonvulsant-stub ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Ammonium Succinate
Ammonium succinate is a chemical compound with the chemical formula . This is an organic ammonium salt of succinic acid. Synthesis Succinic acid reacts with ammonium carbonate to form ammonium succinate. Also, a reaction of ammonia water with succinic acid: :: Physical properties Ammonium succinate forms colorless crystals, easily soluble in water. Thermal decomposition of ammonium succinate produces succinimide. Uses The compound is used a mediator in medicine, lacquer manufacture, and in the production of perfume esters. It is also used in food as a sequestrant A sequestrant is a food additive which improves the quality and stability of foods. A sequestrant forms chelate complexes with polyvalent metal ions, especially copper, iron and nickel. This can prevent the oxidation of the fats in the food. Sequ ..., buffer, and neutralizing agent. References {{ammonium salts Ammonium compounds Succinates ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Royal Society Of Chemistry
The Royal Society of Chemistry (RSC) is a learned society and professional association in the United Kingdom with the goal of "advancing the chemistry, chemical sciences". It was formed in 1980 from the amalgamation of the Chemical Society, the Royal Institute of Chemistry, the Faraday Society, and the Society for Analytical Chemistry with a new Royal Charter and the dual role of learned society and professional body. At its inception, the Society had a combined membership of 49,000 in the world. The headquarters of the Society are at Burlington House, Piccadilly, London. It also has offices in Thomas Graham House in Cambridge (named after Thomas Graham (chemist), Thomas Graham, the first president of the Chemical Society) where ''RSC Publishing'' is based. The Society has offices in the United States, on the campuses of The University of Pennsylvania and Drexel University, at the University City Science Center in Philadelphia, Pennsylvania, in both Beijing and Shanghai, People' ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
