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100311-43-1

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100311-43-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100311-43-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,1 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 100311-43:
(8*1)+(7*0)+(6*0)+(5*3)+(4*1)+(3*1)+(2*4)+(1*3)=41
41 % 10 = 1
So 100311-43-1 is a valid CAS Registry Number.

100311-43-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenylmethoxy-3,5-dipropylbenzoic acid

1.2 Other means of identification

Product number -
Other names BENZOIC ACID,4-(BENZYLOXY)-3,5-DIPROPYL

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:100311-43-1 SDS

100311-43-1Downstream Products

100311-43-1Relevant articles and documents

Pd-catalyzed cross-electrophile Coupling/C-H alkylation reaction enabled by a mediator generatedviaC(sp3)-H activation

Jiang, Hang,Wu, Zhuo,Zhang, Yanghui

, p. 8531 - 8536 (2021/07/02)

Transition-metal-catalyzed cross-electrophile C(sp2)-(sp3) coupling and C-H alkylation reactions represent two efficient methods for the incorporation of an alkyl group into aromatic rings. Herein, we report a Pd-catalyzed cascade cross-electrophile coupling and C-H alkylation reaction of 2-iodo-alkoxylarenes with alkyl chlorides. Methoxy and benzyloxy groups, which are ubiquitous functional groups and common protecting groups, were utilized as crucial mediatorsviaprimary or secondary C(sp3)-H activation. The reaction provides an innovative and convenient access for the synthesis of alkylated phenol derivatives, which are widely found in bioactive compounds and organic functional materials.

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