CAS: 3715-29-5; Sodium 3-Methyl-2-Oxobutanoate

该化合物是一种酸钠盐,其特征是分子结构,包括一个甲基组和一个氯酮功能组,有助于其再活性和溶性.该化合物一般是白色的,白色的晶状粉,在水中可溶解,在各种应用中有用,包括生物化学研究和有机合成中的潜在前体.钠离子的存在可提高其溶解性和稳定性,3-甲基-2-氧丁酸可以参与各种化学反应,包括凝聚和脱色,并经常就其在代谢途径中的作用进行研究.重要的是,要谨慎地处理该化合物,遵守适当的安全规程,如同任何化学物质一样.其应用可能扩大到制药,食品添加剂和生物化学学等领域,可以作为更复杂的分子的建筑块块.

结构式图片

相似化合物

3715-31-9 113-24-6 1173018-24-0

上下游产品

CAS号20201-24-5 3-甲基-2-氧代丁酰乙酯 | CAS号1068-55-9 异丙基氯化镁 | CAS号95-92-1 草酸二乙酯 | CAS号3952-67-8 2-氧代-3-甲基丁酸甲酯 | CAS号59935-29-4 L-缬氨酸-15N | CAS号72-18-4 l-缬氨酸 | CAS号640-68-6 D-缬氨酸 | CAS号759-05-7 3-甲基-2-氧丁酸 | CAS号13031-04-4 二氢-4,4-二甲基-2,3-呋喃二酮 | CAS号79-50-5 DL-泛酰内酯 | CAS号76585-78-9 benzyl 3-methyl... | CAS号77257-02-4 D-[2-2H]valine | CAS号77257-03-5 L-缬氨酸-D1

合成工艺路线路线简述

  • 合成目标产物 Sodium 3-Methyl-2-Oxobutanoate 主要起始原料 Timtec-Bb Sbb005357
  • (文献来源)合成步骤主要原料 Timtec-Bb Sbb005357
3-甲基-2-氧代丁酰乙酯 在 Lithium Hydroxide,水体系中,用 四氢呋喃作为反应溶剂,获得 Sodium 3-Methyl-2-Oxobutyrate
参考文献:[En] Process For Making N-Sulfonated-Amino Acid Derivatives[Fr] Procede De Fabrication De Derives D'Acides Amines N-Sulfones
标题:[En] Process For Making N-Sulfonated-Amino Acid Derivatives[Fr] Procede De Fabrication De Derives D'Acides Amines N-Sulfones

海关参考信息

专利信息


专利号:US-5686275-A
优先权日:1991-12-23
标 题 :Synthesis of homochiral 2-hydroxy acids
发明人:CASEY GUY; LEE THOMAS; LEE ADMINISTRATOR VICTOR; LEE ADMINISTRATRIX EILEEN ANN
权利人:GENZYME LTD
摘要:PCT No. PCT/GB92/02396 Sec. 371 Date Aug. 26, 1994 Sec. 102(e) Date Aug. 26, 1994 PCT Filed Dec. 23, 1992 PCT Pub. No. WO93/13215 PCT Pub. Date Jul. 8, 1993A process for the production of a homochiral 2-hydroxy carboxylic acid or salt thereof corresponding to general formula (I), wherein R represents one of formulae (II), (III), (IV), (V), wherein R' represents straight- or branched-chain alkyl or phenyl optionally para-substituted with methyl, methoxy, nitro or amino; and R'' represents hydrogen, halogen or phenyl optionally para-substituted with methyl, methoxy, nitro or amino; and M represents hydrogen or a salt-forming moiety; characterized in that it comprises reducing a corresponding 2-keto carboxylic acid or salt thereof using a (R)- or (S)-2-oxo carboxylic acid dehydrogenase, inter alia, is disclosed.

专利号:WO-9313215-A1
优先权日:1991-12-23
标 题:Synthesis of homochiral 2-hydroxy acids

专利号:US-7122578-B2
优先权日:2001-09-11
标 题:Method and composition for treating mammalian diseases and injuries which cause pain, erythema, swelling, crusting, ischemia scarring and excess white blood cell infiltration
发明人:MARTIN ALAIN
权利人:MARTIN ALAIN
摘要:A method for treating the disease state in mammals caused by mammalian cells involved in the inflammatory response is disclosed. Mammalian cells participating in the inflammatory response are contacted with an inflammatory suppressor selected from the group consisting of alpha-keto acids and their salts which reduce the undesired inflammatory response and is an antioxidant. The inflammatory suppressor may further provide a cellular energy source and be a building block in the cellular synthesis of other cellular components. Compositions for reducing and treating undesired inflammatory response such as pain, swelling, erythema, crusting, scarring, itching, also disclosed.

专利号:EP-0620857-B1
优先权日:1991-12-23
标题:Synthesis of homochiral 2-hydroxy acids

专利号:EP-0620857-A1
优先权日:1991-12-23
标 题 :Synthesis of homochiral 2-hydroxy acids

专利号:US-9861636-B2
优先权日:2014-04-29
标题 :Polyfluorinated compounds acting as bruton tyrosine kinase inhibitors
发明人:HE WEI
权利人:HE WEI; ZHEJIANG DTRM BIOPHARMA CO LTD
摘要:Described herein is a novel series of multi-fluoro-substituted pyrazolopyrimidine compounds or salts thereof. These compounds are Bruton's tyrosine kinase (BTK) inhibitors. These compounds may possess better BTK inhibition selectivity and pharmacokinetic properties. Disclosed herein are the synthesis methods of these compounds. Disclosed herein are novel synthesis methods of the multi-fluoro-substituted benzophenone and substituted phenoxy benzene. Also disclosed are pharmaceutical compositions comprising the BTK inhibitors described herein. The present invention also relates to pharmaceutical formulations comprising the compounds described herein as active ingredients. The present invention also includes the therapeutic methods by administering the BTK inhibitors and their formulations to treat and inhibit autoimmune disease, hypersensitivity disease, inflammatory diseases and cancer.
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主要参考文献

[参考文献]: Coitinho As, Et Al. Pharmacological Evidence That Alpha-Ketoisovaleric Acid Induces Convulsions Through Gabaergic And Glutamatergic Mechanisms In Rats. Brain Res. 2001 Mar 9;894(1):68-73.
[参考文献]: Maas Wk, Et Al. Alpha-Ketoisovaleric Acid, A Precursor Of Pantothenic Acid In Escherichia Coli. J Bacteriol. 1953 Apr;65(4):388-93.
[参考文献]: Schauder P, Et Al. Oral Administration Of Alpha-Ketoisovaleric Acid Or Valine In Humans: Blood Kinetics And Biochemical Effects. J Lab Clin Med. 1984 Apr;103(4):597-605.
[参考文献]: André Wajner, Et Al. Synaptic Plasma Membrane Na(+), K (+)-Atpase Activity Is Significantly Reduced By The Alpha-Keto Acids Accumulating In Maple Syrup Urine Disease In Rat Cerebral Cortex. Metab Brain Dis. 2007 Mar;22(1):77-88.
[参考文献]: Andreas Schedlbauer, Et Al. Direct Methods And Residue Type Specific Isotope Labeling In Nmr Structure Determination And Model-Driven Sequential Assignment. J Biomol Nmr. 2008 Oct;42(2):111-27.

合成参考文献


参考文献:10.1007/bf01800355
摘要:Langenbeck U, Behbehani A, Mench-Hoinowski A. A synopsis of the unconjugated acidic transamination metabolites of phenylalanine in phenylketonuria. J Inherit Metab Dis. 1992;15(1):136–44. doi: 10.1007/bf01800355.
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