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Product details
4-Bromo-2-methoxypyridine_100367-39-3

4-Bromo-2-methoxypyridine

  • CAS:

    100367-39-3

  • English:

    4-Bromo-2-methoxypyridine

  • Synonym:

    4-Bromo-2-methoxypyridine
    2-methoxy-4-bromopyridine
    4-Bromo-2-Methoxypyridine
    4-Brom-2-methoxy-pyridin
    4-bromo-2-methoxy-pyridine

Details

Chemical Name:4-Bromo-2-methoxypyridine
CAS.NO:100367-39-3
Synonyms:2-methoxy-4-bromopyridine; 
4-Bromo-2-Methoxypyridine; 
4-Brom-2-methoxy-pyridin; 
4-bromo-2-methoxy-pyridine;
Molecular Formula:C6H6BrNO
Molecular Weight:188.02200
 
Physical and Chemical Properties:
Density:1.53;
Boiling point:202.3oC;
Flash point:76.2oC;
 
Specification:
Appearance:Light yellow solid 
Purity:≥99.0%
 
Packing:25 kg/drum, can also be packaged according to customer requirements
Storage:Store in a cool, ventilated place
Application:Intermediate for organic synthesis

Our unique, open innovation partnerships have led to the development of creative strategies and new technologies, giving our customers a distinct market advantage. We build business by creating the best performance chemicals through innovation and collaboration with our partners.We are specialists in chiral chemistry using both chemocatalysis and biocatalysis technologies, but also have practical operating experience over a wide range of modern synthetic reactions.Our company is engaged in the production and custom synthesis of intermediates such as APIs and special chemicals. Relying on our own strong R&D capabilities, we accept custom synthesis of advanced pharmaceutical intermediates, as well as custom synthesis of other types of advanced chemicals, with mature R&D systems and production capacities from gram to tonnage.Our goal is to deliver products that meet our high standards and exceed your expectations, on time, every time.In addition to our core competence in the standard unit operations of organic chemical synthesis, we offer specialised reaction technology, including innovative organometallic synthesis, catalytic transfer hydrogenation and the various operations required for synthesis of chiral compounds.

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