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160417-31-2

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160417-31-2 Usage

General Description

The chemical [1,1'-Biphenyl]-3-carboxylic acid, 4'-methyl-, ethyl ester is an organic compound with the molecular formula C17H16O2. It is an ethyl ester derivative of 4'-methyl-[1,1'-biphenyl]-3-carboxylic acid, which is a derivative of biphenyl carboxylic acid. This chemical compound is commonly used in the production of pharmaceuticals, agrochemicals, and other industrial applications. It is a white to off-white solid with a molecular weight of 252.31 g/mol. The ethyl ester form of this compound makes it more soluble in organic solvents, which contributes to its versatility in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 160417-31-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,4,1 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 160417-31:
(8*1)+(7*6)+(6*0)+(5*4)+(4*1)+(3*7)+(2*3)+(1*1)=102
102 % 10 = 2
So 160417-31-2 is a valid CAS Registry Number.

160417-31-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-(4-methylphenyl)benzoate

1.2 Other means of identification

Product number -
Other names ethyl 4'-methylbiphenyl-3-carboxylate

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:160417-31-2 SDS

160417-31-2Relevant articles and documents

Structure-reactivity relationships in negishi cross-coupling reactions

Dong, Zhi-Bing,Manolikakes, Georg,Shi, Lei,Knochel, Paul,Mayr, Herbert

supporting information; experimental part, p. 248 - 253 (2010/03/30)

Competition experiments have been performed to determine the relative reactivities of substituted bromobenzenes and of different arylzinc reagents in the [Pd(PPh3)4]-catalyzed Negishi cross-coupling reaction in THF at 25 °C. The crosscoupling reactions are accelerated by electron acceptors in the bromobenzenes, the effect of which increases in the order ortho a larger effect than substituent variations in the arylzinc halides (ρ = -0.98).

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