CAS 859932-64-2

Benzeneacetaldehyde,4-chloro-a-oxo-, hydrate (1:1)

Description:

Benzeneacetaldehyde, 4-chloro-α-oxo-, hydrate (1:1) is a chemical compound characterized by its structure, which includes a benzene ring, an aldehyde functional group, and a chloro substituent. The presence of the α-oxo group indicates that it has a carbonyl functionality adjacent to the benzene ring, which can influence its reactivity and interactions. As a hydrate, it contains water molecules in its crystalline structure, which can affect its solubility and stability. This compound may exhibit properties typical of both aldehydes and chlorinated compounds, such as potential reactivity in nucleophilic addition reactions and possible biological activity due to the presence of the chloro group. Its applications could span various fields, including organic synthesis and pharmaceuticals, although specific uses would depend on further research into its properties and behavior in different environments. Safety data should be consulted, as chlorinated compounds can pose health risks.

Formula: C₈H₅ClO₂H₂O

Synonyms:

• Glyoxal,(p-chlorophenyl)-, hydrate (3CI)
• 2-(4-chlorophenyl)-2-oxoacetaldehyde hydrate
• Benzeneacetaldehyde,4-chloro-a-oxo-, hydrate (1:1)
• 2-(4-CHLOROPHENYL)-2-OXOACETALDEHYDE-HYDRATE 1G

Benzeneacetaldehyde,4-chloro-a-oxo-, hydrate (1:1)

CAS: 859932-64-2

Formula: C₈H₇ClO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 186.5924

Ref: IN-DA00IDUH

4-Chlorophenylglyoxal hydrate

CAS: 859932-64-2

4-Chlorophenylglyoxal hydrate

Purity: 95%

Color and Shape: Solid

Molecular weight: 186.59g/mol

Ref: 54-OR1593

2-(4-Chlorophenyl)-2-oxoacetaldehyde hydrate

CAS: 859932-64-2

Purity: 97%

Molecular weight: 186.008

Ref: 10-F569140

4-Chlorophenylglyoxal hydrate

CAS: 859932-64-2

4-Chlorophenylglyoxal hydrate is an antibacterial agent that is synthesized from glyoxal and chloroform. It has a nitro group, which confers antibacterial activity to the compound. 4-Chlorophenylglyoxal hydrate can be reused for up to five cycles without significant loss of its antibacterial activity. This compound has been shown to have high yields with methoxy groups and amines. Synthesis of this compound starts with the reaction of glyoxal and chloroform in an approximate 1:1 ratio. The reaction is carried out at a temperature between 40-60 degrees Celsius for approximately two hours, after which it is cooled to room temperature and filtered. The product is then purified by recrystallization.

Formula: C₈H₇ClO₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 186.59 g/mol

Ref: 3D-JJB93264