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446308-82-3

N-BENZYL 5-BROMO-2-METHOXYBENZENESULFONAMIDE is a chemical compound with the molecular formula C14H14BrNO3S. It is a benzene derivative featuring a sulfonamide functional group, a bromo substitution at the 5 position, and a methoxy substitution at the 2 position. N-BENZYL 5-BROMO-2-METHOXYBENZENESULFONAMIDE is widely utilized in organic synthesis and medicinal chemistry as a building block for creating various biologically active molecules. Its anti-inflammatory and analgesic properties have positioned it as a potential candidate for the development of new pharmaceuticals. Furthermore, it serves as a reagent in chemical reactions for the incorporation of the sulfonamide group into organic molecules.

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  • 446308-82-3 Structure

  • Basic information

    1. Product Name: N-BENZYL 5-BROMO-2-METHOXYBENZENESULFONAMIDE
    2. Synonyms: N-BENZYL 5-BROMO-2-METHOXYBENZENESULFONAMIDE;N-BENZYL 5-BROMO-2-METHOXYBENZENESULPHONAMIDE;N-Benzyl-N-5-bromo-2-methoxybenzenesulphonamide;N-Bezyl 5-bromo-2-methoxybenzenesulphonamide;N-Benzyl-N-5-bromo-2-methoxybenzenesulphonamide 97%;N-Benzyl-N-5-bromo-2-methoxybenzenesulphonamide97%
    3. CAS NO:446308-82-3
    4. Molecular Formula: C14H14BrNO3S
    5. Molecular Weight: 356.23
    6. EINECS: N/A
    7. Product Categories: blocks;Bromides;Sulfonamides
    8. Mol File: 446308-82-3.mol

  • Chemical Properties

    1. Melting Point: 136-140
    2. Boiling Point: 496.9°C at 760 mmHg
    3. Flash Point: 254.3°C
    4. Appearance: /
    5. Density: 1.478g/cm3
    6. Vapor Pressure: 5.18E-10mmHg at 25°C
    7. Refractive Index: 1.602
    8. Storage Temp.: Keep Cold
    9. Solubility: N/A
    10. PKA: 10.39±0.30(Predicted)
    11. CAS DataBase Reference: N-BENZYL 5-BROMO-2-METHOXYBENZENESULFONAMIDE(CAS DataBase Reference)
    12. NIST Chemistry Reference: N-BENZYL 5-BROMO-2-METHOXYBENZENESULFONAMIDE(446308-82-3)
    13. EPA Substance Registry System: N-BENZYL 5-BROMO-2-METHOXYBENZENESULFONAMIDE(446308-82-3)

  • Safety Data

    1. Hazard Codes: Xi
    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: 446308-82-3(Hazardous Substances Data)

446308-82-3 Usage

Uses

Used in Organic Synthesis:
N-BENZYL 5-BROMO-2-METHOXYBENZENESULFONAMIDE is used as a building block in organic synthesis for the creation of biologically active molecules. Its unique structure allows for the development of new compounds with potential applications in various fields.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, N-BENZYL 5-BROMO-2-METHOXYBENZENESULFONAMIDE is used as a precursor for the synthesis of pharmaceuticals. Its anti-inflammatory and analgesic properties make it a promising candidate for the development of new drugs to treat pain and inflammation.
Used as a Reagent in Chemical Reactions:
N-BENZYL 5-BROMO-2-METHOXYBENZENESULFONAMIDE is utilized as a reagent in chemical reactions for the introduction of the sulfonamide group into organic molecules. This group is an important functional group in many pharmaceuticals and agrochemicals, making this compound a valuable tool in the synthesis of various compounds.
Used in Pharmaceutical Development:
Due to its potential anti-inflammatory and analgesic properties, N-BENZYL 5-BROMO-2-METHOXYBENZENESULFONAMIDE is used in the development of new pharmaceuticals. Researchers are exploring its potential as a therapeutic agent for the treatment of pain and inflammation-related conditions.
Used in Research and Development:
N-BENZYL 5-BROMO-2-METHOXYBENZENESULFONAMIDE is also used in research and development settings to study its chemical properties and explore its potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 446308-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,6,3,0 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 446308-82:
(8*4)+(7*4)+(6*6)+(5*3)+(4*0)+(3*8)+(2*8)+(1*2)=153
153 % 10 = 3
So 446308-82-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H14BrNO3S/c1-19-13-8-7-12(15)9-14(13)20(17,18)16-10-11-5-3-2-4-6-11/h2-9,16H,10H2,1H3

446308-82-3SDS

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 N-Benzyl-5-bromo-2-methoxybenzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-benzyl-5-bromo-2-methoxybenzenesulfonamide

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:446308-82-3 SDS

446308-82-3Downstream Products

446308-82-3Relevant articles and documents

Design of Benzoxathiazin-3-one 1,1-Dioxides as a New Class of Irreversible Serine Hydrolase Inhibitors: Discovery of a Uniquely Selective PNPLA4 Inhibitor

Kornahrens, Anne F.,Cognetta, Armand B.,Brody, Daniel M.,Matthews, Megan L.,Cravatt, Benjamin F.,Boger, Dale L.

, p. 7052 - 7061 (2017/05/31)

The design and examination of 4,1,2-benzoxathiazin-3-one 1,1-dioxides as candidate serine hydrolase inhibitors are disclosed, and represent the synthesis and study of a previously unexplored heterocycle. This new class of activated cyclic carbamates provi

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