86070-35-1 Usage
Uses
Used in Pharmaceutical Research:
(S)-2-amino-4-(methylamino)-4-oxobutanoic acid is utilized as a key intermediate in the synthesis of various pharmaceutical compounds due to its unique structural features and reactivity. (S)-2-amino-4-(methylamino)-4-oxobutanoic acid's ability to participate in a range of chemical reactions, including amide, ester, and imine formation, makes it a valuable building block for the development of new drugs with potential therapeutic applications.
Used in Biochemical Reactions:
In the field of biochemistry, (S)-2-amino-4-(methylamino)-4-oxobutanoic acid serves as a versatile reactant for studying enzyme mechanisms, substrate specificity, and the development of novel biocatalysts. Its presence of both amino and carboxylic acid groups allows for interactions with a variety of biomolecules, facilitating investigations into enzyme-substrate interactions and the design of enzyme inhibitors or activators.
Used in Chiral Synthesis:
The chiral nature of (S)-2-amino-4-(methylamino)-4-oxobutanoic acid makes it an attractive candidate for asymmetric synthesis, a technique employed to produce enantiomerically pure compounds. Its specific (2S)-configuration can be exploited to create chiral centers in target molecules, which is particularly important in the pharmaceutical industry where the stereochemistry of a drug can significantly impact its efficacy and safety.
Used in Analytical Chemistry:
(S)-2-amino-4-(methylamino)-4-oxobutanoic acid can be employed as a chiral derivatizing agent in analytical chemistry for the resolution and detection of enantiomers. Its ability to selectively react with specific enantiomers can enhance the separation and identification of chiral compounds in complex mixtures, such as in the analysis of pharmaceuticals, environmental samples, or biological fluids.
Check Digit Verification of cas no
The CAS Registry Mumber 86070-35-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,7 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 86070-35:
(7*8)+(6*6)+(5*0)+(4*7)+(3*0)+(2*3)+(1*5)=131
131 % 10 = 1
So 86070-35-1 is a valid CAS Registry Number.
86070-35-1Relevant academic research and scientific papers
A convenient method of preparation arab League throws cillin sodium
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Paragraph 0033; 0034, (2016/10/10)
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.
β-Lactam antibacterial agents
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, (2008/06/13)
β-Lactam antibiotics having an α-formamido substituent on the carbon atom adjacent to the carbonyl group of the β-lactam ring and in particular bicyclic compounds having the partial structure: STR1 Intermediates and processes for the preparation of the compounds are further disclosed.
