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1H-2,1,3-Benzothiadiazine-4-ol 2,2-dioxide, also known as 1,3-Benzothiadiazine-2,2-dioxide, is a chemical compound with the molecular formula C7H4N2O3S. It is a heterocyclic compound containing a benzene ring fused to a thiadiazine ring, with an oxygen atom attached to the 4-position of the thiadiazine ring and a hydroxyl group at the 4-position of the benzene ring. 1H-2,1,3-Benzothiadiazine-4-ol 2,2-dioxide is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those with insecticidal and herbicidal properties. It is also used in the production of dyes and pigments. Due to its versatile chemical structure, it has attracted significant attention in the field of organic chemistry and has been the subject of various research studies aimed at exploring its potential applications and properties.

2225-37-8

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2225-37-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2225-37-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,2 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2225-37:
(6*2)+(5*2)+(4*2)+(3*5)+(2*3)+(1*7)=58
58 % 10 = 8
So 2225-37-8 is a valid CAS Registry Number.

2225-37-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-2,1,3-benzothiadiazine 2,2-dioxide

1.2 Other means of identification

Product number -
Other names 4-hydroxy-2,1,3-benzothiadiazine dioxide

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:2225-37-8 SDS

2225-37-8Relevant academic research and scientific papers

On the tautomerism of 2,1,3-benzothiadiazinone S,S-dioxide and related compounds

Castro, Ana,Gil, Carmen,Martinez, Ana

, p. 12405 - 12410 (2007/10/03)

Tautomerism of 2,1,3-benzothiadiazinone 2,2-dioxide and other related fused heterocyclic amides has been studied by means of experimental (1H- and 13C-NMR) and theoretical (ab initio calculations) techniques. The synthesis and spectroscopic characterization of mono- and di-blocked derivatives was carried out. The results predict that the keto form is the most abundant tautomer in the gas phase, while the N1(H) hydroxy is the preferred one in solution and the solid state.

Benzothiadiazine dioxide acyclonucleosides as lead compounds for the development of new agents against human cytomegalovirus and varicella-zoster virus infections

Martinez,Esteban,De Clercq

, p. 1031 - 1032 (2007/10/03)

The first acyclonucleosides derived from 2,1,3-benzothiazine dioxides were synthesized. From their antiviral activity evaluation results these compounds might be considered as new leads in the search for inhibitors of human cytomegalovirus (CMV) and varicella-zoster virus (VZV) infections.

SYNTHESE ET CYCLISATION DE CARBOXYLSULFAMIDES DERIVES D'AMINOACIDES

Aouf, Nourreddine,Dewynter, Georges,Montero, Jean-Louis

, p. 6545 - 6546 (2007/10/02)

3-Oxo-4-substituted-1,2,5-thiazolidine 1,1-dioxides are synthesized from the carbosulfamides of amino acids.

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