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3-Bromo-5-chloro-4-methylpyridine, a derivative of pyridine, is a chemical compound with the molecular formula C6H5BrClN. It features a pyridine ring with a bromine atom at the 3rd position, a chlorine atom at the 5th position, and a methyl group at the 4th position. 3-BroMo-5-chloro-4-Methylpyridine is characterized by its clear, colorless to pale yellow liquid appearance and a pungent odor. Due to its flammability, it requires careful handling in well-ventilated areas.

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  • 1260010-08-9 Structure
  • Basic information

    1. Product Name: 3-BroMo-5-chloro-4-Methylpyridine
    2. Synonyms: 3-BroMo-5-chloro-4-Methylpyridine
    3. CAS NO:1260010-08-9
    4. Molecular Formula: C6H5BrClN
    5. Molecular Weight: 206.4676
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1260010-08-9.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.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-BroMo-5-chloro-4-Methylpyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-BroMo-5-chloro-4-Methylpyridine(1260010-08-9)
    11. EPA Substance Registry System: 3-BroMo-5-chloro-4-Methylpyridine(1260010-08-9)
  • 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: 1260010-08-9(Hazardous Substances Data)

1260010-08-9 Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-5-chloro-4-methylpyridine serves as an intermediate in the production of various pharmaceuticals. Its unique structure allows it to be a key component in the synthesis of biologically active compounds, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Bromo-5-chloro-4-methylpyridine is utilized as an intermediate for the synthesis of agrochemicals. Its incorporation into these products can enhance their effectiveness in pest control and crop protection, thereby supporting agricultural productivity.
Used in Fine Chemicals Industry:
3-Bromo-5-chloro-4-methylpyridine also acts as a building block for the synthesis of other fine chemicals. Its versatile structure makes it a valuable component in the creation of specialty chemicals used across various industries, including fragrances, dyes, and advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 1260010-08-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,0,1 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1260010-08:
(9*1)+(8*2)+(7*6)+(6*0)+(5*0)+(4*1)+(3*0)+(2*0)+(1*8)=79
79 % 10 = 9
So 1260010-08-9 is a valid CAS Registry Number.

1260010-08-9SDS

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 3-Bromo-5-chloro-4-methylpyridine

1.2 Other means of identification

Product number -
Other names 3-bromo-5-chloro-4-methyl-pyridine

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:1260010-08-9 SDS

1260010-08-9Upstream product

1260010-08-9Downstream Products

1260010-08-9Relevant articles and documents

ALDOSTERONE SYNTHASE INHIBITORS

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Page/Page column 50; 51, (2012/11/13)

This invention relates to tricyclic triazole analogues of the formula I or their pharmaceutically acceptable salts, wherein the variable are defined herein. The inventive compounds selectively inhibit aldosterone synthetase. This invention also provides for pharmaceutical compositions comprising the compounds of Formula I or their salts as well as to methods for the treatment, amelioration or prevention of conditions that could be treated by inhibiting aldosterone synthetase.

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