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19451-21-9

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19451-21-9 Usage

Structure

Saturated six-membered ring with two sulfur atoms and four carbon atoms, with dithian-2-ylmethyl and methyl substituents

Class

Dithiane derivative

Usage

Building block in organic synthesis, used in reactions such as radical cyclizations and carbon-carbon bond formations

Potential applications

Medicinal chemistry, reagent in organic reactions

Versatility

Widely used in the field of organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 19451-21-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,5 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19451-21:
(7*1)+(6*9)+(5*4)+(4*5)+(3*1)+(2*2)+(1*1)=109
109 % 10 = 9
So 19451-21-9 is a valid CAS Registry Number.

19451-21-9SDS

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-(1,3-dithian-2-ylmethyl)-2-methyl-1,3-dithiane

1.2 Other means of identification

Product number -
Other names (1,3-Dithian-2-yl)(2-methyl-1,3-dithian-2-yl)methane

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:19451-21-9 SDS

19451-21-9Relevant articles and documents

Interrupted oligomerization revisited: Simple and efficient one-pot multicomponent approach to versatile synthetic intermediates

Valiulin, Roman A.,Halliburton, Logan M.,Kutateladze, Andrei G.

, p. 4061 - 4063 (2008/02/11)

A novel multicomponent reaction allowing for a one-pot formation of three carbon-carbon bonds has been developed. It is based on in situ generation and anionic dimerization of methylenedithiane and produces a versatile synthetic equivalent of 4-hydroxy-1,3-alkanediones which, among other things, offers expeditious one-pot access to 3(2H)-furanones.

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