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1-Propanone, 2-methoxy-1,2-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26592-16-5

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26592-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26592-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,9 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26592-16:
(7*2)+(6*6)+(5*5)+(4*9)+(3*2)+(2*1)+(1*6)=125
125 % 10 = 5
So 26592-16-5 is a valid CAS Registry Number.

26592-16-5SDS

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 2-methoxy-1,2-diphenylpropan-1-one

1.2 Other means of identification

Product number -
Other names 1-Propanone,2-methoxy-1,2-diphenyl

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:26592-16-5 SDS

26592-16-5Relevant academic research and scientific papers

Simple phase transfer catalytic method for α-methoxylation of sterically hindered ketones

Abele,Rubina,Shymanska,Lukevics

, p. 1371 - 1376 (2007/10/02)

Reactions of sterically hindered ketones of ArylCOCHR1R2 type (R1, R2 = Me, Et, Ph) with carbon tetrachloride and methyl iodide in the presence of solid KOH and 18-crown-6 afford the corresponding α-methoxyketones [ArylCOC(OMe)R1R2] in one-pot process in 30-67% yields.

Quasi-template Effect: a Tool for Controlling Stereochemistry in Acyclic Systems. Attempted Stereoselective Synthesis of α,α'-Dimethoxystilbene

Inoue, Yoshihisa,Ikeda, Hirokazu,Hakushi, Tadao

, p. 259 - 262 (2007/10/02)

Alkylation with methyl tosylate of stilbenediol dianion, prepared in the reaction of benzoin with a series of alkali-metal hydroxides in THF, gave (E)- and (Z)-α,α'-dimethoxystilbenes as the major products in most cases, the E:Z ratio of which varies from 0.4 to 5.0 depending upon the alkali-metal cation employed; the results are rationalized in the quasi-template effect in an acyclic system and the hard-soft ion principle.

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