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[3-(METHOXYMETHOXY)PHENYL][4-(METHOXYMETHOXY)PHENYL]METHANONE is a chemical compound with the molecular formula C23H22O5. It is a ketone compound that contains two benzene rings, each substituted with methoxymethoxy groups. [3-(METHOXYMETHOXY)PHENYL][4-(METHOXYMETHOXY)PHENYL]METHANONE is often used in organic synthesis and as a building block for creating complex organic molecules. Its unique structure and properties make it a valuable tool for researchers and chemists working in the field of organic chemistry.

263395-66-0

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263395-66-0 Usage

Uses

Used in Organic Synthesis:
[3-(METHOXYMETHOXY)PHENYL][4-(METHOXYMETHOXY)PHENYL]METHANONE is used as a building block for [creating complex organic molecules] because of its unique structure and properties.
Used in Pharmaceutical Industry:
[3-(METHOXYMETHOXY)PHENYL][4-(METHOXYMETHOXY)PHENYL]METHANONE is used as a [chemical intermediate] for [developing new pharmaceutical compounds] due to its potential applications in this field.
Used in Agrochemical Industry:
[3-(METHOXYMETHOXY)PHENYL][4-(METHOXYMETHOXY)PHENYL]METHANONE is used as a [chemical component] for [designing new agrochemicals], as it may have potential applications in this industry.

Check Digit Verification of cas no

The CAS Registry Mumber 263395-66-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,3,3,9 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 263395-66:
(8*2)+(7*6)+(6*3)+(5*3)+(4*9)+(3*5)+(2*6)+(1*6)=160
160 % 10 = 0
So 263395-66-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H18O5/c1-19-11-21-15-8-6-13(7-9-15)17(18)14-4-3-5-16(10-14)22-12-20-2/h3-10H,11-12H2,1-2H3

263395-66-0SDS

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 [3-(methoxymethoxy)phenyl][4-(methoxymethoxy)phenyl]methanone(SALTDATA: FREE)

1.2 Other means of identification

Product number -
Other names -

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:263395-66-0 SDS

263395-66-0Downstream Products

263395-66-0Relevant academic research and scientific papers

New highly stereoselective synthesis of (E)-droloxifene via selective protection of 3,4'-dihydroxybenzophenone and McMurry reaction

Gauthier, Sylvain,Sancéau, Jean-Yves,Mailhot, Josée,Caron, Brigitte,Cloutier, Julie

, p. 703 - 709 (2000)

A new, highly stereoselective synthesis of (E)-droloxifene is reported. Deprotection of 3,4'-dimethoxybenzophenone and selective pivaloylation of the 3'-phenolic position gave 4-hydroxy-3'-(trimethylacetoxy)benzophenone. A McMurry reaction between the preceding benzophenone and propiophenone gave the (E)-olefin as a major product (14:1 E/Z ratio in crude reaction), which was then alkylated with 2-dimethylaminoethyl chloride and deprotected to yield (E)-droloxifene with a > 100:1 E/Z ratio (5 steps, 13%). Attempts to use this strategy as a suitable stereoselective method to obtain (Z)- droloxifene were not successful. (C) 2000 Elsevier Science Ltd.

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