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Benzenesulfinic acid, 1-methylpentyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62750-38-3

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62750-38-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62750-38-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,5 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62750-38:
(7*6)+(6*2)+(5*7)+(4*5)+(3*0)+(2*3)+(1*8)=123
123 % 10 = 3
So 62750-38-3 is a valid CAS Registry Number.

62750-38-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name hexan-2-yl benzenesulfinate

1.2 Other means of identification

Product number -
Other names 1-Methylpentylbenzolsulfinat

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:62750-38-3 SDS

62750-38-3Relevant academic research and scientific papers

ORGANOSULPHUR COMPOUNDS XLVII ALKYLATION OF SULPHINIC ACIDS BY O-ALKYLISOUREAS: O-VERSUS S-REACTIVITY AND ASYMMETRIC SYNTHESIS OF ALKYL SULPHINATES

Kielbasinski, Piotr,Zurawinski, Remigiusz,Drabowitz, Jozef,Mikolajczyk, Marian

, p. 6687 - 6692 (2007/10/02)

The reaction of O-alkylisoureas with sulphinic acids was found to produce the corresponding sulphones and sulphinates, the latter being predominantly formed.The sulphinate to sulphone ratio is strongly influenced by the kind of alkyl groups in the O-alkylisourea and appeared to be also dependent on the solvent used.A few optically active sulphinates (e.e. up to 8.1percent) were prepared in the reaction between benzenesulphinic acid and a series of O-alkylisoureas bearing optically active substituents at the nitrogen atom.A possible reaction mechanism is discussed.

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