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(2,6-dimethoxyphenyl)(2-methoxyphenyl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122547-45-9

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122547-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122547-45-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,5,4 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 122547-45:
(8*1)+(7*2)+(6*2)+(5*5)+(4*4)+(3*7)+(2*4)+(1*5)=109
109 % 10 = 9
So 122547-45-9 is a valid CAS Registry Number.

122547-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,6-dimethoxyphenyl)-(2-methoxyphenyl)methanone

1.2 Other means of identification

Product number -
Other names Methanone,(2,6-dimethoxyphenyl)(2-methoxyphenyl)

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:122547-45-9 SDS

122547-45-9Downstream Products

122547-45-9Relevant academic research and scientific papers

Selective synthetic routes to sterically hindered unsymmetrical diaryl ketones via arylstannanes

Lo Fiego, Marcos J.,Silbestri, Gustavo F.,Chopa, Alicia B.,Lockhart, Maria T.

experimental part, p. 1707 - 1714 (2011/05/17)

Bulky arylstannanes and bulky aroyl chlorides are good reaction partners for the synthesis of two-, three-, and even four-ortho-substituted benzophenones, in good to excellent isolated yields (47-91%). Three simple and direct routes, with differential advantages, are proposed: (i) a catalyst-free protocol, in o-dichlorobenzene (ODCB) at 180 °C; (ii) a room temperature protocol, using AlCl3 (0.5 equiv), in dichloromethane (DCM); and (iii) a solvent-free, indium-promoted procedure. A radical mechanism is proposed for the indium-mediated reactions.2011 American Chemical Society.

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