2-Bromo-3-Chloro-5-(Trifluoromethyl)Pyridine

We are 2-Bromo-3-Chloro-5-(Trifluoromethyl)Pyridine CAS:75806-84-7 manufacturer and supplier in China, Pls send inquiry of to info@nbinno.com of visit www.nbinno.com our official website should you have any interests

Chemical Name:2-Bromo-3-Chloro-5-(Trifluoromethyl)Pyridine
CAS.NO:75806-84-7
Synonyms:2-Bromo-3-Chloro-5-(Trifluoromethyl)Pyridine
 
Physical and Chemical Properties:
Density 1.8±0.1 g/cm3
Boiling Point 226.9±35.0 °C at 760 mmHg
Molecular Formula C6H2BrClF3N
Molecular Weight 260.439
Flash Point 91.0±25.9 °C
 
Specification:
Appearance:Clear, colourless liquidAssay:≥99.0%
 
Packing:25 kg/drum, can also be packaged according to customer requirements
Storage:Store in a cool, ventilated place
Application:Organic synthesis intermediate

2-Bromo-3-Chloro-5-(Trifluoromethyl)Pyridine


Related News: With the onset of the DMF system for APIs, the concentration of the API industry will further increase.1- (trifluorometil) ciclopropanocarboxilato de etilo CAS:139229-57-5 Pre-approval Access Programs (also known as expanded access, early access, compassionate use, named patient supply) are regulatory-compliant processes permitting experimental agents in development to be made available upon the request of a physician or a patient for appropriate patients for whom no alternative treatment option exists in their country.1,9-Decadiene However, pharmaceutical intermediates are subdivided into primary intermediates and advanced intermediates. Because primary intermediate suppliers can only provide simple intermediate production, they are at the front end of the industrial chain. The pressure of competition and price is the greatest. The price fluctuations of basic chemical raw materials have a greater impact on them.(Chloromethyl)trichlorosilane First of all, as an API manufacturer we think of how to make a chemical compound which becomes an API in the laboratory.From the perspective of the corresponding formulation manufacturer, the drug substance needs to meet the requirements of impurities and stability. The production base must pass the international quality system certifications such as cGMP and EuGMP. At the same time, the drug substance company must have sufficient capacity.

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