Welcome to LookChem.com Sign In|Join Free

CAS

  • or
4-BROMO-2-(TRIFLUOROMETHYL)BENZENE SULFONAMIDE is a chemical compound characterized by its molecular formula C7H6BrF3NO2S. It is a white solid with a molecular weight of 295.09 g/mol. 4-BROMO-2-(TRIFLUOROMETHYL)BENZENE SULFONAMIDE is utilized as a pharmaceutical intermediate and serves as a building block in the synthesis of various pharmaceuticals and agrochemicals. Additionally, it is employed as a reagent in organic synthesis and chemical research. Due to its potential to cause skin and eye irritation, it is crucial to handle this compound with care and store it in a cool, dry place away from direct sunlight and heat sources.

351003-62-8 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 351003-62-8 Structure
  • Basic information

    1. Product Name: 4-BROMO-2-(TRIFLUOROMETHYL)BENZENE SULFONAMIDE
    2. Synonyms: SALOR-INT L301078-1EA;4-BROMO-2-(TRIFLUOROMETHYL)BENZENESULPHONAMIDE;4-BROMO-2-(TRIFLUOROMETHYL)BENZENE SULFONAMIDE;4-BROMO-2-(TRIFLLUOROMETHYL)BENZENESULPHONAMIDE;4-Bromo-6-trifluoromethylbenzenesulfonamide;4-Bromo-6-trifluoromethylbenzene;5-Bromo-2-sulphamoylbenzotrifluoride, 2-(Aminosulphonyl)-5-bromobenzotrifluoride
    3. CAS NO:351003-62-8
    4. Molecular Formula: C7H5BrF3NO2S
    5. Molecular Weight: 304.08
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 351003-62-8.mol
  • Chemical Properties

    1. Melting Point: 157-158°C
    2. Boiling Point: 346.6 °C at 760 mmHg
    3. Flash Point: 163.4 °C
    4. Appearance: /
    5. Density: 1.809 g/cm3
    6. Vapor Pressure: 5.71E-05mmHg at 25°C
    7. Refractive Index: 1.529
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-BROMO-2-(TRIFLUOROMETHYL)BENZENE SULFONAMIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-BROMO-2-(TRIFLUOROMETHYL)BENZENE SULFONAMIDE(351003-62-8)
    12. EPA Substance Registry System: 4-BROMO-2-(TRIFLUOROMETHYL)BENZENE SULFONAMIDE(351003-62-8)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 351003-62-8(Hazardous Substances Data)

351003-62-8 Usage

Uses

Used in Pharmaceutical Industry:
4-BROMO-2-(TRIFLUOROMETHYL)BENZENE SULFONAMIDE is used as a pharmaceutical intermediate for the synthesis of various pharmaceuticals. It plays a crucial role in the development of new drugs and contributes to the advancement of medical treatments.
Used in Agrochemical Industry:
In the agrochemical industry, 4-BROMO-2-(TRIFLUOROMETHYL)BENZENE SULFONAMIDE is utilized as a building block in the synthesis of agrochemicals. It aids in the development of new pesticides and other agricultural chemicals, enhancing crop protection and productivity.
Used in Organic Synthesis:
4-BROMO-2-(TRIFLUOROMETHYL)BENZENE SULFONAMIDE is employed as a reagent in organic synthesis. It is instrumental in the creation of various organic compounds, contributing to the advancement of chemical research and the development of new materials and products.
Used in Chemical Research:
As a reagent in chemical research, 4-BROMO-2-(TRIFLUOROMETHYL)BENZENE SULFONAMIDE is used to study chemical reactions and mechanisms. It helps researchers gain insights into the behavior of different chemical compounds and contributes to the understanding of chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 351003-62-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,0,0 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 351003-62:
(8*3)+(7*5)+(6*1)+(5*0)+(4*0)+(3*3)+(2*6)+(1*2)=88
88 % 10 = 8
So 351003-62-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BrF3NO2S/c8-4-1-2-6(15(12,13)14)5(3-4)7(9,10)11/h1-3H,(H2,12,13,14)

351003-62-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Bromo-2-(trifluoromethyl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names 4 -BROMO-2-TRIFLUOROMETHYL-BENZENESULFONAMIDE

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:351003-62-8 SDS

351003-62-8Relevant articles and documents

PHOSPHODIESTERASE INHIBITORS AND USE

-

Paragraph 0112; 0181, (2021/04/02)

The invention provides compounds that may inhibits to ENPP1, and are accordingly useful for treatment disorders related to ENPP1. The invention further provides pharmaceutical compositions containing these compounds and methods of using these compounds to treat or prevent disorders related to ENPP1.

ARYL SULFONAMIDES USEFUL FOR MODULATION OF THE PROGESTERONE RECEPTOR

-

Page/Page column 14, (2008/12/08)

In one embodiment, compounds of the following structure are described, wherein R1 to R7 are described herein. Also provided are methods for preparing these compounds and methods of contraception; treating or preventing fibroids; trea

SUBSTITUTED BIPHENYL DERIVATIVE

-

Page/Page column 148, (2010/11/27)

The present invention relates to a biaryl derivative or a pharmacologically acceptable salt thereof having an excellent collagen-synthesis inhibition activity. A biaryl derivative having a structure represented by the following General Formula (I) or a pharmacologically acceptable salt thereof: wherein R1 represents a C6-C10 aryl group which is substituted with one to three group(s) each independently selected from the group consisting of a group defined by formula R-L-, a di-(C1-C6 alkyl)amino group, a di-(C1-C6 alkyl)aminosulfonyl group, a hydroxyaminocarbonyl group, and a halogen atom, and so on; R represents a C1-C6 alkyl group, and so on; L represents a sulfonyl group, an aminosulfonyl group, or a sulfonylamino group, and so on; R2 represents a hydrogen atom, and so on; A represents a group defined by formula (II), (III), or (IV); R3 represents a C1-C6 alkyl group, and so on; and R4 represents a C1-C6 alkyl group, and so on.

Discovery of a potent CDK2 inhibitor with a novel binding mode, using virtual screening and initial, structure-guided lead scoping

Richardson, Christine M.,Nunns, Claire L.,Williamson, Douglas S.,Parratt, Martin J.,Dokurno, Pawel,Howes, Rob,Borgognoni, Jenifer,Drysdale, Martin J.,Finch, Harry,Hubbard, Roderick E.,Jackson, Philip S.,Kierstan, Peter,Lentzen, Georg,Moore, Jonathan D.,Murray, James B.,Simmonite, Heather,Surgenor, Allan E.,Torrance, Christopher J.

, p. 3880 - 3885 (2008/02/08)

Virtual screening against a pCDK2/cyclin A crystal structure led to the identification of a potent and novel CDK2 inhibitor, which exhibited an unusual mode of interaction with the kinase binding motif. With the aid of X-ray crystallography and modelling,

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 351003-62-8