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Benzene, [(4-methyl-1,2-pentadienyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77084-82-3

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77084-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77084-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,8 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77084-82:
(7*7)+(6*7)+(5*0)+(4*8)+(3*4)+(2*8)+(1*2)=153
153 % 10 = 3
So 77084-82-3 is a valid CAS Registry Number.

77084-82-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylpenta-1,2-dienylsulfanylbenzene

1.2 Other means of identification

Product number -
Other names 4-methyl-1,2-pentadienyl phenyl sulfide

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:77084-82-3 SDS

77084-82-3Relevant academic research and scientific papers

Studies on the regio- and stereoselectivity of halohydroxylation of 1,2-allenyl sulfides or selenides

Ma, Shengming,Hao, Xueshi,Meng, Xiaofeng,Huang, Xian

, p. 5720 - 5724 (2007/10/03)

It was observed that the halohydroxylation of 1,2-allenyl sulfides or selenides with Br2 (CuBr2 or NBS) or I2 and water demonstrated a fairly good regioselectivity (i.e., the C=C bond that is remote from the S or Se atom w

LEAVING GROUP DEPENDENT STEREOCHEMISTRY OF THIOALLENE FORMATION WITH PHENYLTHIOCOPPER PHOSPHINE COMPLEXES

Bridges, Alexander J.,Ross, Robert J.

, p. 4797 - 4800 (2007/10/02)

A Chiral secondary propargylic triflate (5) reacts with phenylthiocopper phosphine complexes (1) and (2) to give propargyl and allenic sulphides with complete inversion of configuration, but the corresponding mesylate (4) reacts with both complexes to give racemic products.

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