1369769-03-8

Basic information

• Product Name: 6-chloro-3-fluoropyridin-2-ol
• Synonyms: 6-chloro-3-fluoropyridin-2-ol
• CAS NO: 1369769-03-8
• Molecular Formula: C₅H₃ClFNO
• Molecular Weight: 147.5348232
• Mol File: 1369769-03-8.mol

Chemical Properties

• Boiling Point: 246.4±40.0 °C(Predicted)
• Appearance: /
• Density: 1.46±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 6.27±0.10(Predicted)
• CAS DataBase Reference: 6-chloro-3-fluoropyridin-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 6-chloro-3-fluoropyridin-2-ol(1369769-03-8)
• EPA Substance Registry System: 6-chloro-3-fluoropyridin-2-ol(1369769-03-8)

Safety Data

• Hazardous Substances Data: 1369769-03-8(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
6-chloro-3-fluoropyridin-2-ol is used as a key intermediate for the synthesis of various drug molecules. Its unique structure and functional groups enable the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Production:
6-chloro-3-fluoropyridin-2-ol is used as a building block in the production of agrochemicals. Its incorporation into agrochemical formulations can enhance the effectiveness of these products in controlling pests and diseases in agriculture.
Used in Specialty Chemicals Manufacturing:
6-chloro-3-fluoropyridin-2-ol is utilized in the manufacturing of various complex molecules for diverse applications in the specialty chemicals industry. Its unique properties allow for the creation of innovative products with specific functionalities.

Upstream product

• 405230-79-7 2-chloro-5-fluoropyridine-1-oxide 
• 31301-51-6 2-chloro-5-fluoropyridine 

Relevant articles and documents

CYCLOPROPANE COMPOUND

A cyclopropane compound represented by the following formula (A) or a pharmaceutically acceptable salt thereof has orexin receptor antagonism, and therefore has a potencial of usefulness for the treatment of sleep disorder for which orexin receptor antagonism is effective, for example, insomnia: wherein Q represents —CH— or a nitrogen atom, R1a and R1b each independently represent a C1-6 alkyl group and the like, R1c represents a hydrogen atom and the like, R2a, R2b, R2c and R2d each independently represent a hydrogen atom, a halogen atom, a C1-6 alkyl group and the like, R3a, R3b and R3c each independently represent a hydrogen atom, a halogen atom and the like, and R3d represents a hydrogen atom and the like.