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89599-01-9

3-BROMOBENZENESULFONAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 89599-01-9 Structure

  • Basic information

    1. Product Name: 3-BROMOBENZENESULFONAMIDE
    2. Synonyms: BUTTPARK 95\57-08;3-BROMOBENZENESULPHONAMIDE;3-BROMOBENZENESULFONAMIDE;3-BROMO-BENZENESULFONIC ACID AMIDE;3-BROMOBENZENE-1-SULFONAMIDE;3-Bromobenzenesulfonamide,97%;m-bromobenzenesulfonamide;3-Bromobenzene-1-Sulphonamide
    3. CAS NO:89599-01-9
    4. Molecular Formula: C6H6BrNO2S
    5. Molecular Weight: 236.09
    6. EINECS: 200-258-5
    7. Product Categories: blocks;Bromides;Sulfonamides;Aryl;Organohalides;Organic Building Blocks;Sulfonamides/Sulfinamides;Sulfur Compounds
    8. Mol File: 89599-01-9.mol

  • Chemical Properties

    1. Melting Point: 151-156 °C(lit.)
    2. Boiling Point: 375.8 °C at 760 mmHg
    3. Flash Point: 181.1 °C
    4. Appearance: white powder
    5. Density: 1.754 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. PKA: 9.81±0.60(Predicted)
    10. CAS DataBase Reference: 3-BROMOBENZENESULFONAMIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-BROMOBENZENESULFONAMIDE(89599-01-9)
    12. EPA Substance Registry System: 3-BROMOBENZENESULFONAMIDE(89599-01-9)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 37/39-26
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 89599-01-9(Hazardous Substances Data)

89599-01-9 Usage

Chemical Properties

white powder

Check Digit Verification of cas no

The CAS Registry Mumber 89599-01-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,9 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89599-01:
(7*8)+(6*9)+(5*5)+(4*9)+(3*9)+(2*0)+(1*1)=199
199 % 10 = 9
So 89599-01-9 is a valid CAS Registry Number.

89599-01-9 Well-known Company Product Price

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  • (Code)Product description
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  • Detail

  • Alfa Aesar

  • (B25681)  3-Bromobenzenesulfonamide, 97%   

  • 89599-01-9

  • 1g

  • 393.0CNY

  • Detail

  • Alfa Aesar

  • (B25681)  3-Bromobenzenesulfonamide, 97%   

  • 89599-01-9

  • 5g

  • 1763.0CNY

  • Detail

  • Aldrich

  • (563609)  3-Bromobenzenesulfonamide  97%

  • 89599-01-9

  • 563609-1G

  • 320.58CNY

  • Detail

89599-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromobenzenesulfonamide

1.2 Other means of identification

Product number -
Other names Benzenesulfonamide, m-bromo-

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:89599-01-9 SDS

89599-01-9Relevant articles and documents

Chemoselective Cleavage of Acylsulfonamides and Sulfonamides by Aluminum Halides

Sang, Dayong,Dong, Bingqian,Liu, Yunfeng,Tian, Juan

, p. 3586 - 3595 (2022/02/25)

The chemoselective cleavage of C-N bonds of amides, sulfonamides, and acylsulfonamides by aluminum halides is described. AlCl3and AlI3display complementary reactivities toward N-alkyl and N-acyl moieties. N-Alkylacylsulfonamides, sec

NOVEL N-ACYL-ARYLSULFONAMIDE DERIVATIVES AS AMINOACYL-TRNA SYNTHETASE INHIBITORS

-

Page/Page column 18; 19, (2016/09/22)

The present invention relates to novel N-acyl-diarysulfonamides acting as inhibitors of bacterial aminoacyl-tRNA synthetase. These can be used as medicines or as constituent of medicines for the treatment of bacterial infections.

Design and synthesis of triazolopyrimidine acylsulfonamides as novel anti-mycobacterial leads acting through inhibition of acetohydroxyacid synthase

Patil, Vikas,Kale, Manoj,Raichurkar, Anandkumar,Bhaskar, Brahatheeswaran,Prahlad, Dwarakanath,Balganesh, Meenakshi,Nandan, Santosh,Shahul Hameed

supporting information, p. 2222 - 2225 (2014/05/06)

Novel triazolopyrimidine acylsulfonamides class of antimycobacterial agents, which are mycobacterial acetohydroxyacid synthase (AHAS) inhibitors were designed by hybridization of known AHAS inhibitors such as sulfonyl urea and triazolopyrimidine sulfonamides. This Letter describes the synthesis and SAR studies of this class of molecules by variation of two parts of the molecule, the phenyl and triazolopyrimidine rings. SAR study describes optimisation of enzyme potency, whole cell potency and evidence of mechanism of action.

Design and synthesis of benzenesulfonamide derivatives as potent anti-influenza hemagglutinin inhibitors

Tang, Guozhi,Lin, Xianfeng,Qiu, Zongxing,Li, Wentao,Zhu, Lei,Wang, Lisha,Li, Shaohua,Li, Haodong,Lin, Wenbin,Yang, Mei,Guo, Tao,Chen, Li,Lee, Daniel,Wu, Jim Z.,Yang, Wengang

supporting information; experimental part, p. 603 - 607 (2011/10/09)

Structural optimization of salicylamide-based hemagglutinin (HA) inhibitor 1 resulted in the identification of cis-3-(5-hydroxy-1,3,3- trimethylcyclohexylmethylamino)benzenesulfonamide 28 and its derivatives as potent anti-influenza agents. The lead compo

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