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Methanone, (2-hydroxy-5-methoxyphenyl)(2-hydroxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83570-57-4

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83570-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83570-57-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,7 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 83570-57:
(7*8)+(6*3)+(5*5)+(4*7)+(3*0)+(2*5)+(1*7)=144
144 % 10 = 4
So 83570-57-4 is a valid CAS Registry Number.

83570-57-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2'-dihydroxy-5-methoxy benzophenone

1.2 Other means of identification

Product number -
Other names 2,2'-dihydroxy-5-methoxybenzophenone

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:83570-57-4 SDS

83570-57-4Relevant academic research and scientific papers

BeCl2 as a new highly selective reagent for dealkylation of aryl-methyl ethers

Sharghi, Hashem,Tamaddon, Fatemeh

, p. 13623 - 13640 (2007/10/03)

An efficient and simple method is introduced for the selective removal of methyl group from poly aryl-methyl ethers, in some important derivatives of benzophenones, xanthones, anthraquinones, aryl esters, benzamides and nitroanisoles with BeCl2.

PHOTOLYSIS OF 2-ARYLOXY- OR 2-ARYLTHIO-1,3-BENZODIOXAN-4-ONES

Diaz-Mondejar, M. Rosa,Miranda, Miguel A.

, p. 1125 - 1131 (2007/10/02)

Photolysis of 1,3-benzodioxan-4-ones 3b and 4a gives mainly products derived from photorearrangement, photoreduction and/or photosolvolysis.These results closely parallel those obtained by irradiation of the isomeric open-chain compounds 1b and 2a.A mechanism involving the intermediacy of radical pairs A and B, generated by successive homolysis of the aryloxy- or arylthio-carbon and carbonyl-oxygen bonds, is proposed.

2'-ACETOXY-2-HYDROXY-5-METHOXYBENZOPHENONE. PHOTOCHEMICAL SYNTHESIS, TRANSACYLATION AND CYCLIZATION TO 2-METHOXYXANTHONE

Diaz-Mondejar, M.R.,Miranda, M.A.

, p. 1523 - 1526 (2007/10/02)

p-Methoxyphenyl salicylate 2 gives 2,2'-dihydroxy-5-methoxybenzophenone 3 upon irradiation, but the yields are low both in hexane and in methanol. p-Methoxyphenyl o-acetoxybenzoate 1 undergoes photo-Fries rearrangement, affording 2'-acetoxy-2-hydroxy-5-methoxybenzophenone 4 in good yield.Compound 4 is not stable in silica gel: it isomerizes to 2'-acetoxy-2-hydroxy-5'-methoxybenzophenone 5, that is also the major acetylation product of 3 with acetyl chloride.Starting from 1, 2-methoxyxanthone 7 is obtained in 57percent overall yield.

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