79068-31-8 Usage
Uses
Used in Pharmaceutical Industry:
1H-Pyrrole-2-carboxylic acid, 3-hydroxy-, methyl ester (9CI) is used as a pharmaceutical intermediate for the synthesis of various drug molecules. Its unique chemical structure allows it to be a versatile building block in the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Organic Synthesis:
1H-Pyrrole-2-carboxylic acid, 3-hydroxy-, methyl ester (9CI) is used as a key intermediate in organic synthesis, particularly in the preparation of complex organic molecules and natural products. Its reactivity and functional groups make it a valuable component in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals.
Used in Research and Development:
1H-Pyrrole-2-carboxylic acid, 3-hydroxy-, methyl ester (9CI) is used as a research compound to study its properties, reactivity, and potential applications. Researchers in academia and industry are interested in exploring its chemical behavior, stability, and interactions with other molecules to gain insights into its potential uses and to develop new synthetic routes and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 79068-31-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,6 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79068-31:
(7*7)+(6*9)+(5*0)+(4*6)+(3*8)+(2*3)+(1*1)=158
158 % 10 = 8
So 79068-31-8 is a valid CAS Registry Number.
79068-31-8Relevant academic research and scientific papers
Synthesis of Proline Compounds cis- and trans-Substituted at C-3
Haeusler, Johannes
, p. 1073 - 1088 (2007/10/02)
Derivatives 1 of 1-pyrroline-2-carboxylic acid react with N-chloro- or N-bromosuccinimide, lead(IV) acetate, and azodicarboxylates to give the compounds 2, 4, and 6.Exchange of halogen in 2 affords the thiocompounds 3.Reduction of 2, 3, 4, and 6 with sodium tetrahydroborate leads to cis- (8dc - 8fc and 8hc - 8kc) but also to trans-configurated (8at and 8bt) amino acids; with amine-borane complexes trans-configurated amino acids are obtained predominantly.The trans-configurated amino acids 8gt -8jt, and 8lt have been synthesized by β-addition of appropriate nucleophils to methyl 1-acetyl-2-pyrroline-2-carboxylate (9a) and subsequent hydrolysis.An improved synthesis of 9a from methyl 1-pyrroline-2-carboxylate (1a) is described.
