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1000587-29-0

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1000587-29-0 Usage

General Description

4'-Methyl-5-nitro-[1,1'-biphenyl]-3-carboxylic acid is a chemical compound with the molecular formula C14H11NO4. It is a derivative of biphenyl, consisting of a biphenyl core with a 4'-methyl and 5-nitro substitution on one of the phenyl rings, and a carboxylic acid group on the other. 4'-Methyl-5-nitro-[1,1'-biphenyl]-3-carboxylic acid has potential applications in the pharmaceutical industry, as it may exhibit biological activity and be useful in the development of new drugs. Additionally, it may also have uses in the field of organic synthesis or as a building block for the creation of other chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1000587-29-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,5,8 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1000587-29:
(9*1)+(8*0)+(7*0)+(6*0)+(5*5)+(4*8)+(3*7)+(2*2)+(1*9)=100
100 % 10 = 0
So 1000587-29-0 is a valid CAS Registry Number.

1000587-29-0SDS

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'-Methyl-5-nitro-[1,1'-biphenyl]-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-(4-methylphenyl)-5-nitrobenzoic 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:1000587-29-0 SDS

1000587-29-0Relevant articles and documents

Regioselective synthesis of carboxylic and fluoromethyl tetrazoles enabled by silver-catalyzed cycloaddition of diazoacetates and aryl diazonium salts

Xiao, Ming-Yang,Chen, Zhen,Zhang, Fa-Guang,Ma, Jun-An

supporting information, (2020/03/04)

Here we present a dipolar [3 + 2] cycloaddition transformation of diazoacetates with arenediazonium salts under silver catalysis, thus offering a straightforward approach for the regioselective construction of carboxylic tetrazoles. Several merits are accompanied with this reaction including readily available starting reagents, broad coupling scope, high yields, and friendly reaction conditions. The synthetic value is further showcased by one-pot conversion of commercially available primary arylamines to tetrazoles and successful transformations of the cycloadducts into valuable 5-fluoromethyltetrazoles and an analogue of P2X3 receptor antagonist.

TETRAZOLE-SUBSTITUTED ARYLAMIDES AS P2X3 AND P2X2/3 ANTAGONISTS

-

, (2015/07/15)

Compounds of the formula I: or a pharmaceutically acceptable salt thereof, wherein, R1 is optionally substituted tetrazolyl, R2 is optionally substituted phenyl, optionally substituted pyridinyl or optionally substituted thienyl, and R3, R4, R5 and R6 are as defined herein. Also provided are methods of using the compounds for treating diseases associated with the P2X3 and/or a P2X2/3 receptor antagonist and methods of making the compounds.

THIADIAZOLE-SUBSTITUTED ARYLAMIDES AS P2X3 AND P2X2/3 ANTAGONISTS

-

Page/Page column 21, (2010/06/22)

Compounds of the formula I: or a pharmaceutically acceptable salt thereof, wherein, R1 is optionally substituted thiadiazolyl, and R2, R3, R4, R5, R6, R7 and R8 are as defined herein. Also disclosed are methods of using the compounds for treating diseases associated with P2X3 and/or a P2X2/3 receptor antagonists and methods of making the compounds.

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