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473-42-7

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473-42-7 Usage

Description

Nitrosulfathiazole, also known as Nisulfazole, is a pale-yellow powder with an odorless and slightly bitter taste. It is slightly soluble in alcohol, very slightly soluble in chloroform, ether, and water, and practically insoluble in benzene. It is a pharmaceutical compound with various applications in different industries.

Uses

Used in Pharmaceutical Industry:
Nitrosulfathiazole is used as an antibiotic agent for treating bacterial infections. It works by inhibiting the synthesis of bacterial cell walls, leading to the death of the bacteria.
Used in Veterinary Medicine:
In the veterinary industry, Nitrosulfathiazole is used as a growth promoter in livestock. It helps in improving the overall health and growth of animals by preventing bacterial infections.
Used in Food Preservation:
Nitrosulfathiazole is also used as a preservative in the food industry. It helps in preventing the growth of bacteria and other microorganisms, thereby extending the shelf life of food products.
Used in Cosmetics Industry:
In the cosmetics industry, Nitrosulfathiazole is used as a preservative in various cosmetic products. It helps in maintaining the freshness and quality of the products by preventing microbial contamination.
Used in Textile Industry:
Nitrosulfathiazole is used in the textile industry as a dye fixative. It helps in improving the colorfastness and durability of dyed fabrics by forming a protective layer around the fibers.
Used in Water Treatment:
In the water treatment industry, Nitrosulfathiazole is used as a disinfectant. It helps in killing bacteria and other harmful microorganisms present in water, ensuring the safety and quality of drinking water.

Check Digit Verification of cas no

The CAS Registry Mumber 473-42-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 473-42:
(5*4)+(4*7)+(3*3)+(2*4)+(1*2)=67
67 % 10 = 7
So 473-42-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H7N3O4S2/c13-12(14)7-1-3-8(4-2-7)18(15,16)11-9-10-5-6-17-9/h1-6H,(H,10,11)

473-42-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nitro-N-(1,3-thiazol-2-yl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names 4-Nitro-benzolsulfonsaeure-thiazol-2-ylamid

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:473-42-7 SDS

473-42-7Relevant articles and documents

3-PHOSPHOGLYCERATE DEHYDROGENASE INHIBITORS AND USES THEREOF

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Paragraph 00282, (2017/10/06)

The present invention provides compounds, compositions thereof, and methods of using the same.

In vivo and in vitro anti-leishmanial activities of 4-nitro-N-pyrimidinand N-pyrazin-2-ylbenzenesulfonamides, and N2-(4-nitrophenyl)-N 1propylglycinamide

Auxiliadora Dea-Ayuela,Castillo, Encarna,Gonzalez-Alvarez, Marta,Vega, Celeste,Rolón, Miriam,Bolas-Fernández, Francisco,Borras, Joaquín,Eugenia González-Rosende

experimental part, p. 7449 - 7456 (2011/02/23)

A series of compounds containing the nitrobenzene and sulfonamido moieties were synthesized and their leishmanicidal effect was assessed in vitro against Leishmania infantum promastigotes. Among the compounds evaluated, the p-nitrobenzenesulfonamides 4Aa

The synthesis and structure-activity relationship studies of selective acetyl-CoA carboxylase inhibitors containing 4-(thiazol-5-yl)but-3-yn-2-amino motif: Polar region modifications

Xu, Xiangdong,Weitzberg, Moshe,Keyes, Robert F.,Li, Qun,Wang, Rongqi,Wang, Xiaojun,Zhang, Xiaolin,Frevert, Ernst U.,Camp, Heidi S.,Beutel, Bruce A.,Sham, Hing L.,Gu, Yu Gui

, p. 1803 - 1807 (2007/10/03)

The structure-activity relationship study focused on the polar region of the HTS hit A-80040 (1) producing several series of potent and selective ACC2 inhibitors. The SAR suggests a compact lipophilic pocket that does not tolerate polar and ionic groups.

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