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N,N-diphenylmethanedisulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85891-81-2

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85891-81-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85891-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,9 and 1 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 85891-81:
(7*8)+(6*5)+(5*8)+(4*9)+(3*1)+(2*8)+(1*1)=182
182 % 10 = 2
So 85891-81-2 is a valid CAS Registry Number.

85891-81-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Methanedisulfonanilide

1.2 Other means of identification

Product number -
Other names Methionsaeure-dianilid

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:85891-81-2 SDS

85891-81-2Relevant academic research and scientific papers

ARYL ESTERS OF THE ACI FORM OF METHANETRISULFONYL FLUORIDE AND THEIR REACTIONS

Yagupol'skii, Yu. L.,Savina, T. I.

, p. 1874 - 1879 (2007/10/02)

The aryl esters of the aci form of methanetrisulfonyl fluoride are formed during the thermal decomposition of the arenediazoniotris(fluorosulfonyl)methanides, which are produced by the action of methanetrisulfonyl fluoride on arenediazonium chlorides.The

ARYL ESTERS OF TRIS(FLUOROSULPHONYL)METHANE ACI FROM

Yagupolskii, Yu. L.,Savina, T. I.,Yufit, D. S.,Struchkov, Yu. T.

, p. 87 - 90 (2007/10/02)

The title compounds are obtained by the thermal decomposition of aryldiazonium tris(fluorosulphonyl)methanides; their structure is proved by the X-ray crystal analysis, NMR 1H and 19F spectra data as well as by chemical transformations.

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