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Benzoyl chloride, 5-(aminosulfonyl)-2,4-dichloro-, is a chemical compound with the molecular formula C7H4Cl2NO3S. It is a derivative of benzoyl chloride, featuring an aminosulfonyl group at the 5-position and two chlorine atoms at the 2 and 4 positions. Benzoyl chloride, 5-(aminosulfonyl)-2,4-dichloro- is known for its reactivity and is often used in the synthesis of various pharmaceuticals and agrochemicals due to its ability to form stable intermediates. It is a white to off-white crystalline solid that is sensitive to moisture and should be handled under anhydrous conditions. The compound is also known for its potential to form hazardous decomposition products and requires careful handling and storage to prevent environmental and health risks.

3740-16-7

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3740-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3740-16-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,4 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3740-16:
(6*3)+(5*7)+(4*4)+(3*0)+(2*1)+(1*6)=77
77 % 10 = 7
So 3740-16-7 is a valid CAS Registry Number.

3740-16-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dichloro-5-sulfamoylbenzoyl chloride

1.2 Other means of identification

Product number -
Other names 4,6-Dichlor-3-sulfamoyl-benzoesaeurechlorid

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:3740-16-7 SDS

3740-16-7Relevant academic research and scientific papers

Intrinsic thermodynamics of high affinity inhibitor binding to recombinant human carbonic anhydrase IV

Mickevi?iūt?, Aurelija,Timm, David D.,Gedgaudas, Marius,Linkuvien?, Vaida,Chen, Zhiwei,Waheed, Abdul,Michailovien?, Vilma,Zubrien?, Asta,Smirnov, Alexey,?apkauskait?, Edita,Baranauskien?, Lina,Jachno, Jelena,Revuckien?, Jurgita,Manakova, Elena,Gra?ulis, Saulius,Matulien?, Jurgita,Di Cera, Enrico,Sly, William S.,Matulis, Daumantas

, p. 271 - 290 (2018)

Membrane-associated carbonic anhydrase (CA) isoform IV participates in carbon metabolism and pH homeostasis and is implicated in the development of eye diseases such as retinitis pigmentosa and glaucoma. A series of substituted benzenesulfonamides were de

Design of two-tail compounds with rotationally fixed benzenesulfonamide ring as inhibitors of carbonic anhydrases

Zak?auskas, Audrius,?apkauskait?, Edita,Jezep?ikas, Linas,Linkuvien?, Vaida,Ki?onait?, Migl?,Smirnov, Alexey,Manakova, Elena,Gra?ulis, Saulius,Matulis, Daumantas

, p. 61 - 78 (2018/07/06)

Rational design of compounds that would bind specific pockets of the target proteins is a difficult task in drug design. The 12 isoforms of catalytically active human carbonic anhydrases (CAs) have highly similar active sites that make it difficult to des

SELECTIVE INHIBITORS OF CARBONIC ANHYDRASE

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Page/Page column 24, (2017/02/24)

Invention is related to novel compounds – benzenesulfonamides of general formulas (I) and (II). The compounds can be used in biomedicine as active ingredients in pharmaceutical formulations, because they inhibit enzymes which participate in disease progre

Carbonic anhydrase inhibitors. Synthesis of a novel series of 5-substituted 2,4-dichlorobenzenesulfonamides and their inhibition of human cytosolic isozymes i and II and the transmembrane tumor-associated isozymes IX and XII

S?awiński, Jaros?aw,Pogorzelska, Aneta,Zo?nowska, Beata,Brozewicz, Kamil,Vullo, Daniela,Supuran, Claudiu T.

, p. 47 - 55 (2014/06/10)

A series of novel 5-substituted 2,4-dichlorobenzenesulfonamides 5a-c, 6a-d, 7a-j and 10a-i have been synthesized and investigated as inhibitors of four isoforms of zinc enzyme carbonic anhydrase (CA.EC 4.2.1.1), that is the cytosolic CA I and II, and tumo

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