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The chemical "2H-Pyrido[3,4-b]indole-2,3-dicarboxylic acid, 1,3,4,9-tetrahydro-, 2-(phenylmethyl) ester, (S)-" is a complex organic compound with a molecular formula of C18H17NO4. It belongs to the class of pyridoindole derivatives, which are heterocyclic compounds with a pyridine and indole ring fused together. This specific compound features a 1,3,4,9-tetrahydro-2H-pyrido[3,4-b]indole core, with two carboxylic acid groups at the 2 and 3 positions, and a phenylmethyl ester group attached to the 2 position. The (S)- configuration indicates that the compound has a specific stereochemistry, with the phenylmethyl group attached to the chiral center in the S configuration. 2H-Pyrido[3,4-b]indole-2,3-dicarboxylic acid, 1,3,4,9-tetrahydro-, 2-(phenylmethyl) ester, (S)- is of interest in the field of medicinal chemistry due to its potential biological activities and applications in drug development.

65491-10-3

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65491-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65491-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,9 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65491-10:
(7*6)+(6*5)+(5*4)+(4*9)+(3*1)+(2*1)+(1*0)=133
133 % 10 = 3
So 65491-10-3 is a valid CAS Registry Number.

65491-10-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,4,9-tetrahydro-β-carboline-2,3-dicarboxylic acid 2-benzyl ester

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:65491-10-3 SDS

65491-10-3Relevant academic research and scientific papers

Synthesis, molecular modeling and QSAR studies in chiral 2,3-disubstituted-1,2,3,4-tetrahydro-9H-pyrido(3,4-b)indoles as potential modulators of opioid antinociception

Saxena, Anil K,Pandey, Suresh K,Tripathi, Ravish C,Raghubir, Ram

, p. 1559 - 1570 (2007/10/03)

In view of coexistence of opioid and cholecystokinin (CCK) in the brain areas concerned with pain processing, some semirigid racemic and chiral anlogues of a potent CCK receptor antagonist (benzotript) have been synthesized and tested for their modulatory

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