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5-Bromo-6-Methylnicotinic acid, a derivative of nicotinic acid, is a chemical compound with the molecular formula C8H7BrNO2. It belongs to the class of organic compounds known as pyridinecarboxylic acids. 5-BroMo-6-Methylnicotinicacid features a bromine atom and a methyl group attached to the pyridine ring, which endows it with unique chemical and biological properties. As a valuable chemical intermediate, 5-Bromo-6-Methylnicotinic acid holds potential pharmaceutical applications, particularly in drug discovery and development.

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  • 1190862-72-6 Structure
  • Basic information

    1. Product Name: 5-BroMo-6-Methylnicotinicacid
    2. Synonyms: 5-BroMo-6-Methylnicotinicacid;3-Pyridinecarboxylic acid, 5-broMo-6-Methyl;5-Bromo-6-methyl-3-pyridinecarboxylic acid;5-Bromo-6-methylpyridin-3-carboxylic acid
    3. CAS NO:1190862-72-6
    4. Molecular Formula: C7H6BrNO2
    5. Molecular Weight: 216.03204
    6. EINECS: 200-258-5
    7. Product Categories: N/A
    8. Mol File: 1190862-72-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 333.0±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.692±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. PKA: 3.25±0.10(Predicted)
    10. CAS DataBase Reference: 5-BroMo-6-Methylnicotinicacid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-BroMo-6-Methylnicotinicacid(1190862-72-6)
    12. EPA Substance Registry System: 5-BroMo-6-Methylnicotinicacid(1190862-72-6)
  • 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: 1190862-72-6(Hazardous Substances Data)

1190862-72-6 Usage

Uses

Used in Pharmaceutical Industry:
5-Bromo-6-Methylnicotinic acid is used as a chemical intermediate for the synthesis of potential drug candidates due to its pharmacological properties. Its unique structure allows it to serve as a building block for the development of bioactive molecules, contributing to the advancement of novel therapeutic agents.
Used in Drug Discovery and Development:
5-Bromo-6-Methylnicotinic acid is utilized as a key component in the creation of new pharmaceutical compounds. Its presence in the molecular structure can influence the biological activity and pharmacokinetic properties of the resulting drug candidates, making it an essential tool in the design and synthesis of innovative medications.

Check Digit Verification of cas no

The CAS Registry Mumber 1190862-72-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,8,6 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1190862-72:
(9*1)+(8*1)+(7*9)+(6*0)+(5*8)+(4*6)+(3*2)+(2*7)+(1*2)=166
166 % 10 = 6
So 1190862-72-6 is a valid CAS Registry Number.

1190862-72-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromo-6-methylnicotinic acid

1.2 Other means of identification

Product number -
Other names 5-bromo-6-methylpyridine-3-carboxylic acid

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:1190862-72-6 SDS

1190862-72-6Downstream Products

1190862-72-6Relevant articles and documents

New substituted spiro[cycloalkyl-1,3'-indo]-2'(1'H)-one derivatives and their use as p38 mitogen-activated kinase inhibitors

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Page/Page column 55-56, (2009/10/21)

This invention is directed to new inhibitors of the p38 mitogen-activated protein kinase having the general formula (I) to processes for their preparation; to pharmaceutical compositions comprising them; and to their use in therapy.

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