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(R)-2-benzyloxycarbonylamino-3-(2-methyl-1H-benzoimidazol-5-yl)-propionic acid methyl ester is a complex organic compound featuring a methyl ester derivative with a benzyloxycarbonyl amine group, a 2-methyl-1H-benzimidazole-5-yl group, and a propionic acid moiety. Its unique molecular structure, which includes functional groups commonly found in bioactive molecules, suggests potential applications in biological and pharmaceutical fields. However, further research is required to explore its properties and uses.

635712-58-2

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635712-58-2 Usage

Uses

Used in Pharmaceutical Industry:
(R)-2-benzyloxycarbonylamino-3-(2-methyl-1H-benzoimidazol-5-yl)-propionic acid methyl ester is used as a potential precursor or intermediate for the synthesis of bioactive molecules due to its complex molecular structure and the presence of functional groups commonly found in pharmaceutical compounds.
Used in Chemical Synthesis:
In the field of organic chemistry, (R)-2-benzyloxycarbonylamino-3-(2-methyl-1H-benzoimidazol-5-yl)-propionic acid methyl ester may serve as a valuable intermediate in the synthesis of other organic compounds, given its unique structure and functional groups.

Check Digit Verification of cas no

The CAS Registry Mumber 635712-58-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,5,7,1 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 635712-58:
(8*6)+(7*3)+(6*5)+(5*7)+(4*1)+(3*2)+(2*5)+(1*8)=162
162 % 10 = 2
So 635712-58-2 is a valid CAS Registry Number.

635712-58-2Relevant academic research and scientific papers

Catalytic asymmetric syntheses of tyrosine surrogates

Han, Xiaojun,Civiello, Rita L.,Fang, Haiquang,Wu, Dedong,Gao, Qi,Chaturvedula, Prasad V.,Macor, John E.,Dubowchik, Gene M.

experimental part, p. 8502 - 8510 (2009/04/04)

(Chemical Equation Presented) Amino acid esters 5-11 as tyrosine mimics have been synthesized in excellent enantioselectivity (up to 99.6% ee) and in good overall chemical yields. The key step in the sequence was the Burk's [Rh(COD)(2R,5R)-Et-DuPhos]BF4-catalyzed asymmetric hydrogenation of enamides with a variety of reactive functional groups.

Calcitonin gene related peptide receptor antagonists

-

, (2008/06/13)

The present invention relates to compounds of Formula (I) as antagonists of calcitonin gene-related peptide receptors (“CGRP-receptor”), pharmaceutical compositions comprising them, methods for identifying them, methods of treatment using them and their use in therapy for treatment of neurogenic vasodilation, neurogenic inflammation, migraine and other headaches, thermal injury, circulatory shock, flushing associated with menopause, airway inflammatory diseases, such as asthma and chronic obstructive pulmonary disease (COPD), and other conditions the treatment of which can be effected by the antagonism of CGRP-receptors.

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