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4H-1-Benzothiopyran-4-one, 2,3-dichloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81576-27-4

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81576-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81576-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,7 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81576-27:
(7*8)+(6*1)+(5*5)+(4*7)+(3*6)+(2*2)+(1*7)=144
144 % 10 = 4
So 81576-27-4 is a valid CAS Registry Number.

81576-27-4SDS

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 2,3-dichlorothiochromen-4-one

1.2 Other means of identification

Product number -
Other names 2,3-dichlorothiochromone

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:81576-27-4 SDS

81576-27-4Downstream Products

81576-27-4Relevant academic research and scientific papers

Ring Contractions of Thiochroman-4-ones and Thiochromen-4-ones

MacKenzie, Neil E.,Thomson, Ronald H.

, p. 395 - 402 (2007/10/02)

3-Bromothiochroman-4-one and its S-oxide undergo ring contraction on heating, especially in the presence of sodium acetate, to give mixtures which include thioindigo (9) and the ethanediylidenethioindigo (10).Brominated 2,2-dimethylthiochroman-4-one reacts on silica gel to form thioindigo, thioindirubin, and the bis(benzothieno)pyran (17).Bromination of thiochromanone gives a number of products, including 2,3-dibromothiochromen-4-one S-oxide which, on heating with sodium acetate in acetic acid, is converted efficiently into thioindigo.The mechanism of this reaction is investigated.

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