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Methyl 3-bromo-6-methoxypicolinate, a chemical compound with the molecular formula C8H8BrNO3, is a derivative of picolinic acid, a heterocyclic compound with a pyridine ring. It is a brominated and methoxylated derivative of 3-methylpicolinic acid, known for its unique structure and chemical properties. This versatile building block is commonly used in organic synthesis and pharmaceutical research, making it a valuable component in the development of new chemical compounds.

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  • 1214332-49-6 Structure
  • Basic information

    1. Product Name: Methyl 3-broMo-6-Methoxypicolinate
    2. Synonyms: Methyl 3-broMo-6-Methoxypicolinate;3-Bromo-6-methoxy-pyridine-2-carboxylic acid methyl ester
    3. CAS NO:1214332-49-6
    4. Molecular Formula: C8H8BrNO3
    5. Molecular Weight: 246.05802
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1214332-49-6.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: Methyl 3-broMo-6-Methoxypicolinate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 3-broMo-6-Methoxypicolinate(1214332-49-6)
    11. EPA Substance Registry System: Methyl 3-broMo-6-Methoxypicolinate(1214332-49-6)
  • 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: 1214332-49-6(Hazardous Substances Data)

1214332-49-6 Usage

Uses

Used in Pharmaceutical Research:
Methyl 3-bromo-6-methoxypicolinate is used as a key intermediate in the synthesis of various pharmaceuticals for its potential applications in the production of drugs. Its unique structure allows for the development of bioactive compounds with therapeutic properties.
Used in Agrochemical Production:
In the agrochemical industry, Methyl 3-bromo-6-methoxypicolinate is utilized as an intermediate in the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used in Organic Synthesis:
Methyl 3-bromo-6-methoxypicolinate serves as a versatile building block in organic synthesis, enabling the creation of a wide range of chemical compounds for various applications across different industries. Its unique chemical properties make it an essential component in the synthesis process.

Check Digit Verification of cas no

The CAS Registry Mumber 1214332-49-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,4,3,3 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1214332-49:
(9*1)+(8*2)+(7*1)+(6*4)+(5*3)+(4*3)+(3*2)+(2*4)+(1*9)=106
106 % 10 = 6
So 1214332-49-6 is a valid CAS Registry Number.

1214332-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3-bromo-6-methoxypicolinate

1.2 Other means of identification

Product number -
Other names methyl 3-bromo-6-methoxypyridine-2-carboxylate

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:1214332-49-6 SDS

1214332-49-6Relevant articles and documents

SHP2 PHOSPHATASE INHIBITORS AND METHODS OF USE THEREOF

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Paragraph 0233, (2019/10/15)

The present disclosure relates to novel compounds including formula (X) and pharmaceutical compositions thereof, and methods for inhibiting the activity of SHP2 phosphatase with the compounds and compositions of the disclosure. The present disclosure further relates to, but is not limited to, methods for treating disorders associated with SHP2 deregulation with the compounds and compositions of the disclosure.

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