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Benzene, [(6-bromo-1-cyclohexen-1-yl)sulfonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

396728-95-3

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396728-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 396728-95-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,6,7,2 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 396728-95:
(8*3)+(7*9)+(6*6)+(5*7)+(4*2)+(3*8)+(2*9)+(1*5)=213
213 % 10 = 3
So 396728-95-3 is a valid CAS Registry Number.

396728-95-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (6-bromocyclohexen-1-yl)sulfonylbenzene

1.2 Other means of identification

Product number -
Other names 1-(phenylsulfonyl)-6-bromocyclohexene

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:396728-95-3 SDS

396728-95-3Relevant academic research and scientific papers

Improved and environmentally friendly large-scale preparation of cyclohexadienyl-, cycloheptadienyl sulfone and enantiopure epoxy cycloheptyl sulfones

Park, Taesik,Torres, Eduardo,Fuchs, Philip L.

, p. 1895 - 1900 (2007/10/03)

Kilogram-scale amounts of cycloheptadienyl phenylsulfone and cyclohexadienyl phenylsulfone were prepared by one operation in 5 stages with over 50% yield and requiring no purification. A practical and efficient method for the Jacobsen asymmetric epoxidati

Economical and environmentally friendly syntheses of 2-(phenylsulfonyl)-1,3-cyclohexadiene and 2-(phenylsulfonyl)-1,3-cycloheptadiene

Meyers, David J.,Fuchs, Philip L.

, p. 200 - 204 (2007/10/03)

A large-scale and inexpensive synthesis of dienes 1 and 2 has been developed via a four-step procedure starting with benzenethiol and the corresponding cyclic ketone. No chromatography is required.

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