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4H-1,3-Benzoxazin-4-one, 6-chloro-2,3-dihydro-2-thioxo- is a complex organic chemical compound with the molecular formula C7H4ClNO2S. It belongs to the class of benzoxazinone derivatives, which are heterocyclic compounds containing oxygen and nitrogen atoms in their structure. This specific compound features a benzene ring fused to an oxazine ring, with a 6-chloro substituent and a 2-thioxo group. It is a colorless solid and is used in various chemical research and pharmaceutical applications. Due to its complex structure, it is essential to handle 4H-1,3-Benzoxazin-4-one, 6-chloro-2,3-dihydro-2-thioxo- with care and follow proper safety guidelines.

774-32-3

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774-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 774-32-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 774-32:
(5*7)+(4*7)+(3*4)+(2*3)+(1*2)=83
83 % 10 = 3
So 774-32-3 is a valid CAS Registry Number.

774-32-3Downstream Products

774-32-3Relevant academic research and scientific papers

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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