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2,2,2-trichloroethyl methanesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57392-58-2

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57392-58-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57392-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,9 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57392-58:
(7*5)+(6*7)+(5*3)+(4*9)+(3*2)+(2*5)+(1*8)=152
152 % 10 = 2
So 57392-58-2 is a valid CAS Registry Number.

57392-58-2SDS

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 2,2,2-trichloroethyl methanesulfonate

1.2 Other means of identification

Product number -
Other names ghl.PD_Mitscher_leg0.722

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:57392-58-2 SDS

57392-58-2Downstream Products

57392-58-2Relevant academic research and scientific papers

Method for sulphonylating a hydroxylated organic compound

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Page 8, (2010/11/30)

The invention concerns a method for sulphonylating a hydroxylated organic compound. The invention concerns in particular aliphatic hydroxylated compounds and more particularly those which comprise on their aliphatic chain, an electroattractive group. The

A method of hydroxylation org. compd. sulfonylated

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Page 22, (2010/02/14)

The invention concerns a method for sulphonylating a hydroxylated organic compound. The invention concerns in particular aliphatic hydroxylated compounds and more particularly those which comprise on their aliphatic chain, an electroattractive group. The

Conformational Equilibria due to Ring Inversion in N-Alkyl-cis-decahydroisoquinolines

Bailey, Judith M.,Booth, Harold,Al-Shirayda, Hatif A. R. Y.

, p. 583 - 588 (2007/10/02)

The position of conformational equilibria due to ring inversion in N-alkyl-cis-decahydroisoquinolines (alkyl = Me, Et, Pri, CH2CF3, or CH2CCl3) has been assessed directly from 13C and/or 19F n.m.r. spectra recorded at temperatures between 173 and 253 K.The measured equilibrium constants are related to the inductive effect of the N-substituent which produces an increase (Me, Et, Pri) or decrease (CH2CF3, CH2CCl3) in the magnitude of the gauche propylamine-type repulsive interaction. 13C Chemical shifts are tabulated for the carbon atoms of the two twin-chair conformations undergoing exchange.

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