86070-35-1

Basic information

• Product Name: (S)-2-amino-4-(methylamino)-4-oxobutanoic acid
• Synonyms: (S)-2-Amino-N-methyl-succinamic acid;(S)-2-amino-4-(methylamino)-4-oxobutanoic acid
• CAS NO: 86070-35-1
• Molecular Formula: C5H10N2O3
• Molecular Weight: 146.14
• Mol File: 86070-35-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 413.3±40.0 °C(Predicted)
• Appearance: /
• Density: 1.263±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 2.49±0.10(Predicted)
• CAS DataBase Reference: (S)-2-amino-4-(methylamino)-4-oxobutanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-amino-4-(methylamino)-4-oxobutanoic acid(86070-35-1)
• EPA Substance Registry System: (S)-2-amino-4-(methylamino)-4-oxobutanoic acid(86070-35-1)

Safety Data

• Hazardous Substances Data: 86070-35-1(Hazardous Substances Data)

Usage

General Description

"(S)-2-amino-4-(methylamino)-4-oxobutanoic acid" is a chemical compound possessing multiple functional groups including an amino group, a carboxylic acid group, and a ketone group. Its IUPAC name is (2S)-2-amino-4-(methylamino)-4-oxobutanoic acid. The presence of an S in parenthesis before the chemical name denotes that it is a chiral compound, indicating its specific configuration in three-dimensional space - in this case, signifying that it has a left-handed configuration. Another important feature of this chemical is the methylamino group which refers to an amino group (-NH2) where one of the hydrogen atoms has been replaced by a methyl group (-CH3). The exact properties and uses of this chemical compound would depend on its specific reactions with other chemicals. However, its arrangement suggests it may have a role in biochemical reactions or could be used for pharmaceutical research.

Upstream product

• 4070-43-3 L-aspartic acid-4-ethyl ester 
• 74-89-5 methylamine 
• 22728-89-8 D-2-amino-3-methoxycarbonylpropionic acid hydrochloride 

Relevant articles and documents

A convenient method of preparation arab League throws cillin sodium

The invention discloses a convenient method for preparing aspoxicillin sodium. The method comprises the steps of adding D-aspartic acid into a mixed solution of thionyl chloride and methanol, reacting to prepare D-aspartic acid methyl ester hydrochloride, reacting the D-aspartic acid methyl ester hydrochloride with an aqueous solution of methylamine to obtain aspartic formamide, protecting the first amino on the aspartic formamide by using trifluoroacetyl, then reacting the aspartic formamide with carbonyldimidazole to form an active mixed acid anhydride, condensing the active mixed acid anhydride with an amoxicillin triethylamine salt, finally removing the protective ground and forming a sodium salt under the alkali condition to obtain a crude aspoxicillin product of the target product, and refining the crude product to obtain the high-purity aspoxicillin sodium finished product. The method has the advantages that the reagents are cheap, readily available and low in toxicity and environmental pressure, the process operation is compact and stable, the purity of the product is high and the like.

Influence of alkylamides of glutamic acid and related compounds on the central nervous system. II. Syntheses of amides of gutamic acid and related compounds, and their effects on the central nervous system.

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