CAS 14731-10-3

3-(CHLOROMETHYL)-5-PHENYLISOXAZOLE

Description:

3-(Chloromethyl)-5-phenylisoxazole is an organic compound characterized by its isoxazole ring, which is a five-membered heterocyclic structure containing both nitrogen and oxygen atoms. The presence of a chloromethyl group (-CH2Cl) at the 3-position and a phenyl group (-C6H5) at the 5-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific solvent used. It is of interest in various fields, including medicinal chemistry, due to its potential biological activities. The chloromethyl group can serve as a reactive site for further chemical modifications, making it a versatile intermediate in organic synthesis. Additionally, the isoxazole moiety is known for its involvement in various pharmacological activities, which may include anti-inflammatory and antimicrobial properties. As with many organic compounds, safety precautions should be taken when handling this substance, as it may pose health risks if ingested or inhaled.

Formula: C₁₀H₈ClNO

InChI: InChI=1/C10H8ClNO/c11-7-9-6-10(13-12-9)8-4-2-1-3-5-8/h1-6H,7H2

SMILES: c1ccc(cc1)c1cc(CCl)no1

Synonyms:

• 3-(Chloromethyl)-5-phenylisoxazole 97%
• 3-(Chloromethyl)-5-Phenyl-1,2-Oxazole

Isoxazole, 3-(chloromethyl)-5-phenyl-

CAS: 14731-10-3

Formula: C₁₀H₈ClNO

Purity: 95%

Color and Shape: Solid

Molecular weight: 193.6296

Ref: IN-DA001ESF

3-(Chloromethyl)-5-phenylisoxazole

CAS: 14731-10-3

3-(Chloromethyl)-5-phenylisoxazole

Formula: C₁₀H₈ClNO

Purity: 97%

Color and Shape: brown crystalline solid

Molecular weight: 193.63g/mol

Ref: 54-OR9185

3-(Chloromethyl)-5-phenylisoxazole

CAS: 14731-10-3

Formula: C₁₀H₈ClNO

Purity: 95.0%

Molecular weight: 193.63

Ref: 10-F321926

3-(Chloromethyl)-5-phenylisoxazole

CAS: 14731-10-3

3-(Chloromethyl)-5-phenylisoxazole is a water soluble moiety that is used in the synthesis of conjugates with antitumor activity. 3-(Chloromethyl)-5-phenylisoxazole has been shown to inhibit the growth of brain tumors by binding to DNA, inhibiting transcription and replication. The drug also inhibits protein synthesis and cell division. This compound can be esterified and isothiazole substituted to form an antitumor drug that has a strong antiproliferative effect on human leukemia cells. The biological activity of 3-(chloromethyl)-5-phenylisoxazole can be enhanced by catalytic hydrogenation with methanol in acidic conditions.

Formula: C₁₀H₈ClNO

Purity: Min. 95%

Molecular weight: 193.63 g/mol

Ref: 3D-PAA73110