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5350-70-9

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5350-70-9 Usage

General Description

1-(benzylsulfanyl)-3-(prop-2-en-1-yloxy)propan-2-ol is a chemical compound with a molecular formula C13H18O2S. It is a derivative of propan-2-ol and contains a benzylsulfanyl group and a prop-2-en-1-yloxy group. 1-(benzylsulfanyl)-3-(prop-2-en-1-yloxy)propan-2-ol has potential uses in organic synthesis and pharmaceutical research. It is important to handle this chemical with care and ensure proper safety measures are in place when working with it.

Check Digit Verification of cas no

The CAS Registry Mumber 5350-70-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5350-70:
(6*5)+(5*3)+(4*5)+(3*0)+(2*7)+(1*0)=79
79 % 10 = 9
So 5350-70-9 is a valid CAS Registry Number.

5350-70-9SDS

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 2-methyl-2,3-diphenylbutanenitrile

1.2 Other means of identification

Product number -
Other names 2-methyl-2,3-diphenyl-butanenitrile

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:5350-70-9 SDS

5350-70-9Downstream Products

5350-70-9Relevant articles and documents

Oxidative nucleophilic substitution of hydrogen in nitroarenes with phenylacetonitrile derivatives

Makosza, Mieczyslaw,Stalinski, Krzysztof

, p. 8797 - 8810 (2007/10/03)

Tertiary carbanions generated from α-substituted phenylacetonitriles in liquid ammonia add to nitrobenzenes in the para position to form the corresponding σ(H)-adducts which are transformed, depending on the starting nitriles and the reaction conditions, to products of oxidative nucleophilic substitution of hydrogen, ONSH or vicarious nucleophilic substitution, VNS.

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