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4513-73-9

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4513-73-9 Usage

General Description

4-Methoxy-3-methylphenylacetic acid is an organic compound with the chemical formula C10H12O3. It is a white crystalline powder that is commonly used in the synthesis of pharmaceutical drugs and as a building block in the production of various organic compounds. This chemical is a derivative of acetic acid and contains a methoxy and a methyl group attached to a phenyl ring. It is used as a precursor in the synthesis of various pharmaceuticals and has potential applications in the development of new drugs and biologically active compounds. Additionally, it may have uses in the development of new materials and chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 4513-73-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,1 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4513-73:
(6*4)+(5*5)+(4*1)+(3*3)+(2*7)+(1*3)=79
79 % 10 = 9
So 4513-73-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3/c1-7-5-8(6-10(11)12)3-4-9(7)13-2/h3-5H,6H2,1-2H3,(H,11,12)

4513-73-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methoxy-3-Methylphenylacetic Acid

1.2 Other means of identification

Product number -
Other names 2-(4-Methoxy-3-methylphenyl)acetic acid

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4513-73-9 SDS

4513-73-9Relevant articles and documents

Quinolones as gonadotropin releasing hormone (GnRH) antagonists: Simultaneous optimization of the C(3)-aryl and C(6)-substituents

Young, Jonathan R.,Huang, Song X.,Chen, Irene,Walsh, Thomas F.,DeVita, Robert J.,Wyvratt Jr., Matthew J.,Goulet, Mark T.,Ren, Ning,Lo, Jane,Yang, Yi Tien,Yudkovitz, Joel B.,Cheng, Kang,Smith, Roy G.

, p. 1723 - 1727 (2007/10/03)

A series of 3-arylquinolones was prepared and evaluated for their ability to act as gonadotropin releasing hormone (GnRH) antagonists. A variety of substitution patterns of the 3-aryl substituent are described. The 3,4,5-trimethylphenyl substituent (23h) was found to be optimal. (C) 2000 Elsevier Science Ltd. All rights reserved.

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