CAS 167073-07-6

(1S,2R)-2-fluorocyclopropane-1-carboxylic acid

Description:

(1S,2R)-2-fluorocyclopropane-1-carboxylic acid is a chiral compound characterized by its cyclopropane ring structure, which is a three-membered carbon ring. The presence of a fluorine atom at the second carbon position and a carboxylic acid functional group at the first carbon contributes to its unique chemical properties. This compound is typically a colorless liquid or solid, depending on the temperature and purity. Its chirality indicates that it exists in two enantiomeric forms, with the (1S,2R) configuration being one specific stereoisomer. The carboxylic acid group makes it acidic, allowing it to participate in various chemical reactions, such as esterification and amidation. Additionally, the fluorine substituent can influence the compound's reactivity and stability, often enhancing its lipophilicity and biological activity. This compound may have applications in pharmaceuticals and agrochemicals, where fluorinated compounds are often sought for their unique properties. Safety data should be consulted for handling and storage, as with any chemical substance.

Formula: C₄H₅FO₂

Synonyms:

• Cyclopropanecarboxylic acid, 2-fluoro-, (1S,2R)-

Cyclopropanecarboxylic acid, 2-fluoro-, (1S,2R)-

CAS: 167073-07-6

Formula: C₄H₅FO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 104.0797

Ref: IN-DA001X3Y

(1S,2R)-2-Fluorocyclopropanecarboxylic acid

CAS: 167073-07-6

(1S,2R)-2-Fluorocyclopropanecarboxylic acid

Purity: 98%

Color and Shape: White Solid

Molecular weight: 0.00g/mol

Ref: 54-PC400538

(1S,2R)-2-Fluorocyclopropanecarboxylic acid

CAS: 167073-07-6

Purity: 97%

Color and Shape: Solid

Molecular weight: 104.0800018

Ref: 10-F603011