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1214342-44-5

3-Bromo-5-fluorobenzene-1-sulfonyl chloride is an organic chemical compound characterized by its bromine and fluorine substitutions on the benzene ring, along with a sulfonyl chloride functional group. 3-BroMo-5-fluorobenzene-1-sulfonyl chloride is known for its reactivity and utility in the synthesis of various pharmaceutically relevant molecules.

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  • 1214342-44-5 Structure

  • Basic information

    1. Product Name: 3-BroMo-5-fluorobenzene-1-sulfonyl chloride
    2. Synonyms: 3-BroMo-5-fluorobenzene-1-sulfonyl chloride;3-Bromo-5-fluorobenzenesulfonyl chloride;3-bromo-5-fluorophenylsulfonyl chloride
    3. CAS NO:1214342-44-5
    4. Molecular Formula: C6H3BrClFO2S
    5. Molecular Weight: 273.5072232
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1214342-44-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 301.9±27.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.867±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-BroMo-5-fluorobenzene-1-sulfonyl chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-BroMo-5-fluorobenzene-1-sulfonyl chloride(1214342-44-5)
    11. EPA Substance Registry System: 3-BroMo-5-fluorobenzene-1-sulfonyl chloride(1214342-44-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1214342-44-5(Hazardous Substances Data)

1214342-44-5 Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-5-fluorobenzene-1-sulfonyl chloride is used as a key reactant for the synthesis of tetrahydropyridopyrimidines and tetrahydropyridopyridines. These synthesized compounds serve as inhibitors of HBsAg (Hepatitis B surface antigen) and HBV DNA (Hepatitis B virus DNA) production, which are crucial for the treatment of hepatitis B virus infections. By targeting these specific viral components, the compound contributes to the development of potential therapeutics against hepatitis B.

Check Digit Verification of cas no

The CAS Registry Mumber 1214342-44-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,4,3,4 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1214342-44:
(9*1)+(8*2)+(7*1)+(6*4)+(5*3)+(4*4)+(3*2)+(2*4)+(1*4)=105
105 % 10 = 5
So 1214342-44-5 is a valid CAS Registry Number.

1214342-44-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromo-5-fluorobenzene-1-sulfonyl chloride

1.2 Other means of identification

Product number -
Other names 3-Bromo-5-fluorobenzenesulfonyl chloride

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:1214342-44-5 SDS

1214342-44-5Downstream Products

1214342-44-5Relevant articles and documents

TETRAHYDROPYRIDOPYRIMIDINES AND TETRAHYDROPYRIDOPYRIDINES AS INHIBITORS OF HBSAG (HBV SURFACE ANTIGEN) AND HBV DNA PRODUCTION FOR THE TREATMENT OF HEPATITIS B VIRUS INFECTIONS

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Page/Page column 245, (2016/11/21)

The present invention provides tetrahydropyridopyrimidines and tetrahydropyridopyridines having the general formula (I) wherein R1, R2, U, W, X, Y and Z are as described herein, as inhibitors of HBsAg (HBV surface antigen) and HBV DNA production for the treatment and prophylaxis of hepatitis B virus infections.

INDOLIZINE DERIVATIVES AS PHOSHOINOSITIDE 3-KINASES INHIBITORS

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Paragraph 0769; 0770, (2015/12/31)

Compounds of formula (I), defined herein, inhibit phosphoinositide 3-kinases (PI3K) and are useful for the treatment of disorders associated with PI3K enzymes.

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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