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Benzenesulfonamide, N-[4-(aminosulfonyl)phenyl]-, also known as sulfisoxazole, is a synthetic chemical compound belonging to the class of sulfonamide antibiotics. It is a white crystalline powder with the chemical formula C12H13N3O4S2. Sulfonamides, including sulfisoxazole, work by inhibiting bacterial synthesis of folic acid, which is essential for bacterial growth and reproduction. Benzenesulfonamide, N-[4-(aminosulfonyl)phenyl]- is primarily used to treat various bacterial infections, such as urinary tract infections, respiratory infections, and otitis media, by interfering with the bacteria's ability to produce folic acid. However, its use has declined due to the emergence of antibiotic-resistant bacteria and the availability of more effective antibiotics.

4461-11-4

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4461-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4461-11-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,6 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4461-11:
(6*4)+(5*4)+(4*6)+(3*1)+(2*1)+(1*1)=74
74 % 10 = 4
So 4461-11-4 is a valid CAS Registry Number.

4461-11-4SDS

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 4-(benzenesulfonamido)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-Benzolsulfonyl-sulfanilsaeure-amid

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:4461-11-4 SDS

4461-11-4Downstream Products

4461-11-4Relevant academic research and scientific papers

Carbonic anhydrase inhibitors. Part 61. Quantum chemical QSAR of a group of benzenedisulfonamides

Clare, Brian W.,Supuran, Claudiu T.

, p. 463 - 474 (2007/10/03)

The synthesis of a large group of benzenesulfonamides containing both a primary and secondary sulfonamide moiety is described. These compounds are powerful inhibitors of several isozymes of the enzyme carbonic anhydrase. Separate QSAR's are given for inhi

Syntheses of N4-(Alkyl or arylsulfonyl)sulfanilyl Derivatives

Cremlyn, R. J.,Swinbourne, F. J.,Devlukia, P.,Shode, O.

, p. 249 - 253 (2007/10/02)

2,4-Dichloro, 2,5-dichloro and 3,4-dichloro-benzene-sulfanilides react with chlorosulfonic acid at low temperature to give good yields of the corresponding dichlorobenzenesulfonyl sulfanilyl chlorides.A number of chlorides have been converted into derivatives by reaction with nucleophiles, such as dimethylamine, hydrazine and sodium azide.N4-Acetamidobenzenesulfonylsulfanilyl derivatives have been prepared by the condensation of N4-acetylsulfanilyl chloride with the appropriate sulfanilyl derivative.Methylsulfonanilide reacts with chlorosulfonic acid to give N4-(methylsulfonyl)sulfanilyl chloride.The compounds have been tested for their antibacterial and antifungal activity.

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