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161912-36-3

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161912-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161912-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,9,1 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 161912-36:
(8*1)+(7*6)+(6*1)+(5*9)+(4*1)+(3*2)+(2*3)+(1*6)=123
123 % 10 = 3
So 161912-36-3 is a valid CAS Registry Number.

161912-36-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,3,4,5,6-pentafluorophenyl) methanesulfonate

1.2 Other means of identification

Product number -
Other names pentafluorophenylmethanesulfonate

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:161912-36-3 SDS

161912-36-3Downstream Products

161912-36-3Relevant articles and documents

Method for preparing pentafluorophenyl methanesulfonate at low cost

-

Paragraph 0037-0040, (2019/02/13)

The invention discloses a method for preparing pentafluorophenyl methanesulfonate. The method comprises the following steps: dissolving pentafluorophenol in an organic solvent, and then adding an acidbinding agent to form a mixed solution; dropwise adding

Direct Synthesis of Sulfonamides and Activated Sulfonate Esters from Sulfonic Acids

Caddick, Stephen,Wilden, Jonathan D.,Judd, Duncan B.

, p. 1024 - 1025 (2007/10/03)

A general new method for the preparation of sulfonamides and activated sulfonate esters by the direct coupling of sulfonic acid salts with amines and alcohols using the reagent triphenylphosphine ditriflate is described. A new reusable polymer-supported reagent for these transformations under heterogeneous conditions is also described. These methods provide a fundamentally new approach to making small molecules containing the sulfonamide functional group. Copyright

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