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2,2'-(1,3-Dithietane-2,4-diylidene)bis(N-methylacetamide) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27123-79-1

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27123-79-1 Usage

Physical state

Colorless liquid at room temperature

Usage

Building block for various organic compounds in organic synthesis

Properties

Strong nucleophilic and basic

Applications

Production of dithietanes and other sulfur-containing compounds, potential use in pharmaceuticals and materials science

Handling precautions

Proper care and caution due to strong reactivity and potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 27123-79-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,1,2 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 27123-79:
(7*2)+(6*7)+(5*1)+(4*2)+(3*3)+(2*7)+(1*9)=101
101 % 10 = 1
So 27123-79-1 is a valid CAS Registry Number.

27123-79-1SDS

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-[4-[2-(methylamino)-2-oxoethylidene]-1,3-dithietan-2-ylidene]acetamide

1.2 Other means of identification

Product number -
Other names 2,4-Bis-(N-methylcarboxamido)-methylen-1,3-dithietan

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:27123-79-1 SDS

27123-79-1Downstream Products

27123-79-1Relevant academic research and scientific papers

SYNTHESIS OF 2-SUBSTITUTED 3(2H)-ISOTHIAZOLONES FROM 2-SUBSTITUTED 5-AROYL-3(2H)-ISOTHIAZOLONES

Tsolomitis, Athanase,Sandris, Constantine

, p. 569 - 575 (2007/10/02)

2-Substituted 3(2H)-isothiazolones 3 have been prepared from 2-substituted 5-aroyl-3(2H)-isothiazolones 6, which are readily available from N-substituted 3-aroylpropionamides 5.The nucleophilic displacement on the 5-aroyl group was found to proceed easily and quantitatively when a benzene solution of compound 6 was stirred at room temperature either with 10percent sodium hydroxide solution or with solid sodium hydroxide.

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