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Methyl 2-hydroxybiphenyl-4-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

198994-00-2

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198994-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 198994-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,9,9 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 198994-00:
(8*1)+(7*9)+(6*8)+(5*9)+(4*9)+(3*4)+(2*0)+(1*0)=212
212 % 10 = 2
So 198994-00-2 is a valid CAS Registry Number.

198994-00-2SDS

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 methyl 3-hydroxy-4-phenylbenzoate

1.2 Other means of identification

Product number -
Other names Methyl 2-hydroxybiphenyl-4-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:198994-00-2 SDS

198994-00-2Downstream Products

198994-00-2Relevant academic research and scientific papers

Recent progress on the iterative construction of 4-substituted-3-hydroxy benzoic acids from unsaturated aldehydes and dimethyl succinate

Brenna, Elisabetta,Fuganti, Claudio,Perozzo, Valentina,Serra, Stefano

, p. 15029 - 15040 (1997)

An improvement of a known two step cyclization procedure, affording 4-aryl-3-hydroxy benzoic acid derivatives from 3-aryl-2,3-unsaturated aldehydes and dimethyl succinate, is described. The high versatility of the synthetic procedure is shown, as the aryl substituent can be a benzene or naphthalene moiety, or an heteroaromatic ring. It can be applied iteratively to prepare p,p'-oligophenyl derivatives.

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