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72731-11-4

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72731-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72731-11-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,3 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72731-11:
(7*7)+(6*2)+(5*7)+(4*3)+(3*1)+(2*1)+(1*1)=114
114 % 10 = 4
So 72731-11-4 is a valid CAS Registry Number.

72731-11-4SDS

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 α-(methylthio)-α-allylacetophenone

1.2 Other means of identification

Product number -
Other names 2-Methylmercapto-1-phenyl-pent-4-en-1-on

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:72731-11-4 SDS

72731-11-4Downstream Products

72731-11-4Relevant articles and documents

Nickelocene-Lithium Aluminum Hydride: A Versatile Desulfurization Reagent

Chan, Man-Chor,Cheng, Kwok-Man,Ho, Kim Man,Ng, Chi Tat,Yam, Tsz Man,et al.

, p. 4466 - 4471 (2007/10/02)

A new homogeneous organonickel reagent prepared from nickelocene and LiAlH4 has been shown to be effective for the reduction of the carbon-sulfur bonds of thiols, thioethers, sulfoxides, and sulfones to the corresponding carbon-hydrogen bonds.Functional groups such as isolated double bonds, esters, and carbonyls as well as halides remain intact under the reaction conditions.Preliminary studies on the nature of the reagent and the mechanism for the reaction have been carried out by employing deuterium labeling experiments and spectroscopic methods.Metal hydridic species may play an important role in these reactions.The reagent can also be used to reduce the carbon-carbon double bond of conjugate enones and catalyze hydrogenation of carbon-carbon multiple bonds.A comparison of the reaction behavior of this newly developed reagent with that of Raney nickel is discussed.

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