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N-Cyclopropyl 2-bromobenzenesulfonamide is a chemical compound that belongs to the class of sulfonamides, which are commonly used as antimicrobial agents. It is characterized by its white crystalline solid appearance and solubility in organic solvents. With a molecular formula of C9H10BrNO2S, this compound features a cyclopropyl group and a bromine atom, which confer unique chemical properties and reactivity. It may serve as a potential drug candidate in medicinal chemistry or as an intermediate in organic synthesis, with its specific applications and effects contingent upon further research and testing.

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  • 951883-93-5 Structure
  • Basic information

    1. Product Name: N-Cyclopropyl 2-bromobenzenesulfonamide
    2. Synonyms: 2-Bromo-N-cyclopropylbenzenesulfonamide;N-Cyclopropyl 2-bromobenzenesulfonamide
    3. CAS NO:951883-93-5
    4. Molecular Formula: C9H10BrNO2S
    5. Molecular Weight: 276.15
    6. EINECS: N/A
    7. Product Categories: blocks;Bromides;Sulfonamides
    8. Mol File: 951883-93-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: N-Cyclopropyl 2-bromobenzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-Cyclopropyl 2-bromobenzenesulfonamide(951883-93-5)
    11. EPA Substance Registry System: N-Cyclopropyl 2-bromobenzenesulfonamide(951883-93-5)
  • 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: 951883-93-5(Hazardous Substances Data)

951883-93-5 Usage

Uses

Used in Pharmaceutical Industry:
N-Cyclopropyl 2-bromobenzenesulfonamide is used as a potential drug candidate for its antimicrobial properties, given its classification within the sulfonamide class of compounds. Its unique structural features, including the cyclopropyl group and bromine atom, may contribute to its effectiveness in treating microbial infections.
Used in Organic Synthesis:
In the field of organic synthesis, N-Cyclopropyl 2-bromobenzenesulfonamide is utilized as an intermediate. Its specific chemical properties and reactivity make it a valuable component in the synthesis of more complex organic compounds, potentially leading to the development of new pharmaceuticals or other chemical products.
Used in Medicinal Chemistry Research:
N-Cyclopropyl 2-bromobenzenesulfonamide is employed in medicinal chemistry research to explore its potential as a new therapeutic agent. Further studies are required to understand its mechanism of action, efficacy, and safety profile, which will determine its suitability for clinical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 951883-93-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,1,8,8 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 951883-93:
(8*9)+(7*5)+(6*1)+(5*8)+(4*8)+(3*3)+(2*9)+(1*3)=215
215 % 10 = 5
So 951883-93-5 is a valid CAS Registry Number.

951883-93-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-N-cyclopropylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names 2-bromo-N-cyclopropylbenzenesulfonamide

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:951883-93-5 SDS

951883-93-5Downstream Products

951883-93-5Relevant articles and documents

Diastereoselective Photoredox-Catalyzed [3 + 2] Cycloadditions of N-Sulfonyl Cyclopropylamines with Electron-Deficient Olefins

White, Dawn H.,Noble, Adam,Booker-Milburn, Kevin I.,Aggarwal, Varinder K.

supporting information, p. 3038 - 3042 (2021/05/04)

A highly diastereoselective, visible-light-induced [3 + 2] cycloaddition between N-sulfonyl cyclopropylamines and electron-deficient olefins is reported. The reactions proceed via the oxidation of a sulfonamide aza-anion by an organic photocatalyst to generate a nitrogen-centered radical. Strain-induced ring opening and intermolecular addition to the olefin generate an intermediate carbon-centered radical that is reduced to an anion prior to 5-exo cyclization. This enables a highly diastereoselective construction of trans-cyclopentanes possessing synthetically useful functional groups.

FLAP MODULATORS

-

Paragraph 0197; 0199, (2015/11/03)

The present invention relates to compounds of Formula (I), or a form thereof, wherein ring A, R1, R2, R3, R3′, L, W, and V are as defined herein, useful as FLAP modulators. The invention also relates to pharmaceutical compositions comprising compounds of Formula (I). Methods of making and using the compounds of Formula (I) are also within the scope of the invention

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