CAS 133662-20-1

1-(2-chlorophenyl)-2-hydroxyethanone

Description:

1-(2-Chlorophenyl)-2-hydroxyethanone, also known as a chlorinated phenolic compound, is characterized by its molecular structure, which includes a hydroxyl group (-OH) and a ketone functional group (C=O) attached to a two-carbon ethane backbone. The presence of the 2-chlorophenyl group contributes to its aromatic properties and influences its reactivity and solubility. This compound typically exhibits moderate polarity due to the hydroxyl group, which can engage in hydrogen bonding, enhancing its solubility in polar solvents. It may also display biological activity, making it of interest in pharmaceutical and agrochemical research. The compound's stability can be affected by environmental conditions, and it may undergo various chemical reactions, including oxidation and substitution. Safety data should be consulted, as chlorinated compounds can pose health risks and environmental concerns. Overall, 1-(2-chlorophenyl)-2-hydroxyethanone is a versatile compound with potential applications in various fields, including organic synthesis and medicinal chemistry.

Formula: C₈H₇ClO₂

Synonyms:

• Tulobuterol Impurity 7
• 1-(2-chlorophenyl)-2-hydroxyethanone
• 2’-Chloro-2-hydroxyacetophenone
• 1-(2-Chlorophenyl)-2-hydroxyethan-1-one
• Ethanone, 1-(2-chlorophenyl)-2-hydroxy-
• 2a€-Chloro-2-hydroxyacetophenone

1-(2-Chlorophenyl)-2-hydroxyethan-1-one

CAS: 133662-20-1

Formula: C₈H₇ClO₂

Purity: 95%

Color and Shape: Liquid

Molecular weight: 170.5930

Ref: IN-DA003G9J

1-(2-Chlorophenyl)-2-hydroxyethanone

CAS: 133662-20-1

1-(2-Chlorophenyl)-2-hydroxyethanone

Purity: 98%

Ref: 54-OR1037426

1-(2-Chlorophenyl)-2-hydroxyethanone

CAS: 133662-20-1

Purity: 98%

Molecular weight: 170.5899963

Ref: 10-F718388

2'-Chloro-2-hydroxyacetophenone

CAS: 133662-20-1

2'-Chloro-2-hydroxyacetophenone is a chiral compound that is used as an intermediate in the synthesis of other compounds. The enantiomerically pure form of 2'-chloro-2-hydroxyacetophenone can be obtained by catalytic asymmetric reduction of 2,2-dichloroacetophenone. The two enantiomers are optically active and can be separated by column chromatography. C. parapsilosis produces the racemic mixture of 2'-chloro-2-hydroxyacetophenone, while Candida candida produces only the (R) enantiomer.

Formula: C₈H₇ClO₂

Purity: Min. 95%

Molecular weight: 170.59 g/mol

Ref: 3D-IFA66220