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

77084-83-4

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77084-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77084-83-4 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 77084-83:
(7*7)+(6*7)+(5*0)+(4*8)+(3*4)+(2*8)+(1*3)=154
154 % 10 = 4
So 77084-83-4 is a valid CAS Registry Number.

77084-83-4SDS

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-methylpent-1-yn-3-yl)(phenyl)sulfane

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:77084-83-4 SDS

77084-83-4Relevant academic research and scientific papers

Gold-Catalyzed Oxidative Hydrative Alkenylations of Propargyl Aryl Thioethers with Quinoline N-Oxides Involving a 1,3-Sulfur Migration

Wagh, Sachin Bhausaheb,Singh, Rahulkumar Rajmani,Sahani, Rajkumar Lalji,Liu, Rai-Shung

, p. 2755 - 2758 (2019/04/30)

This work reports gold-catalyzed oxidative alkenylations of quinoline N-oxides with propargyl aryl thioethers to afford 3-hydroxy-1-alkylidenephenylthiopropan-2-one via a 1,3-sulfur group migration. The mechanism of this reaction is postulated to involve

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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