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7672-94-8

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7672-94-8 Usage

Uses

Agricultural chemical.

Hazard

A poison by ingestion.

Safety Profile

A poison by ingestion. When heated to decomposition it emits toxic vapors of NOx SOx and Cl-.

Check Digit Verification of cas no

The CAS Registry Mumber 7672-94-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,7 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7672-94:
(6*7)+(5*6)+(4*7)+(3*2)+(2*9)+(1*4)=128
128 % 10 = 8
So 7672-94-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H4ClNO2S/c9-4-1-2-6-5(3-4)7(11)10-8(13)12-6/h1-3H,(H,10,11,13)

7672-94-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-2-sulfanylidene-1,3-benzoxazin-4-one

1.2 Other means of identification

Product number -
Other names -

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:7672-94-8 SDS

7672-94-8Downstream Products

7672-94-8Relevant articles and documents

Generalized method for the production of 1,3-benzoxazine, 1,3-benzothiazine, and quinazoline derivatives from 2-(hydroxy, thio, or amino) aromatic acids using triphenylphosphine thiocyanogen

Pritchard, Kaylene M.,Al-Rawi, Jasim M.,Hughes, Andrew B.

, p. 1601 - 1611 (2007/10/03)

A modified one-pot method was developed for the synthesis of 1,3-benzoxazines, in which the preparation of unstable thiocyanogen was omitted. The method was found to be general for substituted (methyl, methoxy, halo, and hydroxy) 2-hydroxy benzoic acids and 2-hydroxy naphthoic acids. The method was extended to 2-thio, 2-amino, and N-methyl aminobenzoic acid with which the synthesis of 1,3-benzothiazine and quinazoline derivatives has been achieved, respectively. It was also found that 3-hydroxypyridine-2-carboxylic acid and 2-hydroxynicotinic acid using a modified method gave 2-thioxo-2,3-dihydro-4H- pyrido[2,3-e][1,3]oxazin-4-one and 2-thioxo-2,3-dihydro-4H-pyrido[3,2-e][1,3] oxazin-4-one, respectively. The structures of the new compounds were confirmed by the analysis of their IR, 1H, and 13C NMR spectra. Copyright Taylor & Francis, Inc.

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