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102-46-5

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102-46-5 Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 32, p. 1757, 1989 DOI: 10.1021/jm00128a016

Check Digit Verification of cas no

The CAS Registry Mumber 102-46-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 102-46:
(5*1)+(4*0)+(3*2)+(2*4)+(1*6)=25
25 % 10 = 5
So 102-46-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H11Cl/c1-7-3-4-9(6-10)5-8(7)2/h3-5H,6H2,1-2H3

102-46-5SDS

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 3,4-Dimethylbenzyl chloride

1.2 Other means of identification

Product number -
Other names 1-(Chloromethyl)-3,4-dimethylbenzene (contains isomer)

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:102-46-5 SDS

102-46-5Relevant articles and documents

Improved preparation of 3,3′,4,4′-tetramethyldiphenylethane by self coupling reaciton in aqueous media

Hu, Yu-Lin,Lu, Ming,Liu, Qi-Fa,Ge, Qiang

, p. 1056 - 1063 (2009)

In this article, 3,3′,4,4′-tetramethyldiphenylethane was obtained in 86.5% total yield by self coupling reaction of 3,4-dimethylbenzyl chloride catalyzed by Cu/Cu/2/Cl/2//PEG-600 and promoted by iron in aqueous media and the starting

Mechanism of solvolysis of substituted benzyl chlorides in aqueous ethanol

Denegri, Bernard,Mati?, Mirela,Va?ko, Monika

supporting information, (2021/11/22)

The mechanism of solvolyses of activated ortho-, meta- and para-substituted benzyl chlorides in aqueous ethanol has been studied by using the Hammett-Brown and Yukawa-Tsuno treatments as well as by correlating logarithms of solvolysis rate constants with relative stabilities of corresponding benzyl carbocations in water calculated at the IEFPCM-M06–2X/6-311+G(3df,3pd) level of theory. Benzyl chlorides containing strong conjugative electron-donors in the para-position solvolyze by the SN1 mechanism, whereas other activated benzyl chlorides solvolyze by the SN2 mechanism via loose transition states.

BENZODIAZEPINONE COMPOUNDS AND METHODS OF TREATMENT USING SAME

-

Page/Page column 65, (2011/04/19)

The invention provides 1,4-benzodiazepinone compounds, pharmaceutical compositions, and methods of treating autoimmune disorders, chronic inflammatory disorders, and hyperproliferative disorders. For example, the 1,4-benzodiazepinone compounds and pharmaceutical compositions are contemplated to be useful for treating rheumatoid arthritis, graft-versus-host disease, inflammatory bowel disease, and the like.

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