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Benzenepropanoic acid, 3-methyl-α-oxo, also known as 3-methyl-α-oxobenzenepentanoic acid or 3-methyl-α-oxo-benzenepropanoic acid, is an organic compound with the chemical formula C10H10O3. It is a derivative of benzenepropanoic acid, featuring a methyl group at the 3rd carbon position and an α-oxo (keto) group at the 2nd carbon position. Benzenepropanoic acid, 3-Methyl-.alpha.-oxo- is a white crystalline solid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its chemical structure and properties make it a versatile building block in the development of new compounds with potential applications in various industries.

61676-25-3

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61676-25-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61676-25-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,7 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61676-25:
(7*6)+(6*1)+(5*6)+(4*7)+(3*6)+(2*2)+(1*5)=133
133 % 10 = 3
So 61676-25-3 is a valid CAS Registry Number.

61676-25-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxo-3-m-tolyl-propionic acid

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:61676-25-3 SDS

61676-25-3Relevant academic research and scientific papers

2-OXO-1,2,4,5-TETRAHYDRO-1,3-BENZODIAZEPIN-3-YL-PIPERIDINES USED AS CGRP ANTAGONISTS

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Page/Page column 78, (2010/11/24)

The invention relates to novel CGRP antagonists of general formula (I), in which B, R1 and R2 are defined as cited in claim 1, to their tautomers, isomers, diastereomers, enantiomers, hydrates, mixtures and salts, in addition to the hydrates of their salts, in particular their physiologically compatible salts, with inorganic or organic acids or bases. The invention also relates to medicaments containing said compounds, to their use and to a method for their production.

SELECTED CGRP ANTAGONISTS, METHODS FOR THE PRODUCTION THEREOF AND THEIR USE AS MEDICAMENTS

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Page/Page column 247, (2008/06/13)

The invention relates to CGRP antagonists of general formula (I), in which A, X, D, E, G, M, Q and R1 to R3 are defined as in Claim 1, to their tautomers, isomers, diastereomers, enantiomers, hydrates, mixtures and their salts as well as the hydrates of the salts, particularly their physiologically compatible salts having inorganic or organic acids, to medicaments containing these compounds, to their use, and to methods for the production thereof.

Synthesis and activity of novel analogs of hemiasterlin as inhibitors of tubulin polymerization: Modification of the a segment

Yamashita, Ayako,Norton, Emily B.,Kaplan, Joshua A.,Niu, Chuan,Loganzo, Frank,Hernandez, Richard,Beyer, Carl F.,Annable, Tami,Musto, Sylvia,Discafani, Carolyn,Zask, Arie,Ayral-Kaloustian, Semiramis

, p. 5317 - 5322 (2007/10/03)

Analogs of HTI-286 (1), containing various aromatic rings in the A segment, were synthesized as potential inhibitors of tubulin polymerization, and the structure-activity relationships related to stereo- and regio-chemical effects of substituents on the a

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