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16358-40-0

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16358-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16358-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,5 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16358-40:
(7*1)+(6*6)+(5*3)+(4*5)+(3*8)+(2*4)+(1*0)=110
110 % 10 = 0
So 16358-40-0 is a valid CAS Registry Number.

16358-40-0SDS

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 N-octylmethanesulfonamide

1.2 Other means of identification

Product number -
Other names N-Octyl-mercaptoethyl-guanidin-CS2

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:16358-40-0 SDS

16358-40-0Downstream Products

16358-40-0Relevant articles and documents

Copper-Catalyzed, N-Directed Csp3-H Trifluoromethylthiolation (-SCF3) and Trifluoromethylselenation (-SeCF3)

Modak, Atanu,Pinter, Emily N.,Cook, Silas P.

supporting information, p. 18405 - 18410 (2019/11/19)

A direct and versatile copper-catalyzed trifluoromethylthiolation and trifluoromethylselenation of primary, secondary, and tertiary aliphatic C-H bonds was developed. The reaction provides direct access to molecules containing these emerging moieties in the presence of a wide range of common functional groups and in complex molecular environments.

Reductive deprotection of allyl, benzyl and sulfonyl substituted alcohols, amines and amides using a naphthalene-catalysed lithiation

Alonso, Emma,Ramon, Diego J.,Yus, Miguel

, p. 14355 - 14368 (2007/10/03)

The reaction of different protected alcohols, amines and amides with lithium and a catalytic amount of naphthalene (4 mol %) in THF at low temperature leads to their deprotection under very mild reaction conditions, the process being in many cases chemoselective.

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