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3-Bromo-2-vinylpyridine, with the molecular formula C7H6BrN, is a colorless to light yellow liquid that exhibits a faint odor. It is a chemical compound that serves as a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as a building block in the production of various organic compounds. Its ability to be polymerized makes it a valuable component in the formation of different polymers.

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  • 799246-56-3 Structure
  • Basic information

    1. Product Name: 3-BroMo-2-vinylpyridine
    2. Synonyms: 3-BroMo-2-vinylpyridine
    3. CAS NO:799246-56-3
    4. Molecular Formula: C7H6BrN
    5. Molecular Weight: 184.03324
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 799246-56-3.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: 3-BroMo-2-vinylpyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-BroMo-2-vinylpyridine(799246-56-3)
    11. EPA Substance Registry System: 3-BroMo-2-vinylpyridine(799246-56-3)
  • 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: 799246-56-3(Hazardous Substances Data)

799246-56-3 Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-2-vinylpyridine is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications, contributing to the advancement of medicine and healthcare.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Bromo-2-vinylpyridine is utilized as an intermediate for the production of agrochemicals. Its role in creating effective pesticides and other agricultural chemicals helps to improve crop protection and yield.
Used in Organic Compounds Production:
3-Bromo-2-vinylpyridine is used as a building block in the synthesis of a wide range of organic compounds. Its versatility in chemical reactions enables the creation of diverse molecules with various applications in different industries.
Used in Polymer Production:
3-Bromo-2-vinylpyridine is used in the polymerization process to form various polymers. These polymers have potential uses in multiple industries, including plastics, coatings, and adhesives, due to their unique properties derived from the 3-Bromo-2-vinylpyridine monomer.

Check Digit Verification of cas no

The CAS Registry Mumber 799246-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,9,2,4 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 799246-56:
(8*7)+(7*9)+(6*9)+(5*2)+(4*4)+(3*6)+(2*5)+(1*6)=233
233 % 10 = 3
So 799246-56-3 is a valid CAS Registry Number.

799246-56-3SDS

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-2-vinylpyridine

1.2 Other means of identification

Product number -
Other names 3-bromo-2-ethenylpyridine

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:799246-56-3 SDS

799246-56-3Relevant articles and documents

Enantioselective Construction of Spiro Quaternary Carbon Stereocenters via Pd-Catalyzed Intramolecular α-Arylation

Wu, Ting,Kang, Xuehua,Bai, Heng,Xiong, Wenrui,Xu, Guangqing,Tang, Wenjun,Tang, Wenjun

supporting information, p. 4602 - 4607 (2020/06/29)

We herein report the development of a sterically hindered and electron-rich P-chiral monophosphorus biaryl ligand that has enabled a general and efficient enantioselective intramolecular α-arylation, providing access to a wide series of [4.4], [4.5], and [4.6]-spirocycles with chiral benzylic quaternary carbons in high yields with good to excellent enantioselectivities. A pronounced water effect on enantioselectivity is observed.

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