CAS 771-98-2

1-Phenylcyclohexene

Description:

1-Phenylcyclohexene is an organic compound characterized by its bicyclic structure, which consists of a cyclohexene ring fused with a phenyl group. This compound is classified as an alkene due to the presence of a double bond within the cyclohexene ring. It typically appears as a colorless to pale yellow liquid with a distinctive aromatic odor. The molecular formula of 1-Phenylcyclohexene is C12H14, and it has a relatively low boiling point, indicating that it can exist as a vapor at room temperature. This compound is known for its reactivity, particularly in electrophilic addition reactions due to the presence of the double bond. It is also used in various chemical syntheses and can serve as a precursor for more complex organic molecules. Additionally, 1-Phenylcyclohexene is of interest in materials science and polymer chemistry, where it may be utilized in the development of new materials. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested.

Formula: C₁₂H₁₄

InChI: InChI=1S/C12H14/c1-3-7-11(8-4-1)12-9-5-2-6-10-12/h1,3-4,7-9H,2,5-6,10H2

InChI key: InChIKey=WCMSFBRREKZZFL-UHFFFAOYSA-N

SMILES: C=1(CCCCC1)C2=CC=CC=C2

Synonyms:

• 1-Cyclohexen-1-ylbenzene
• 1-Cyclohexenylbenzene~2,3,4,5-Tetrahydrobiphenyl
• 1-Phenylcyclohexene
• 2,3,4,5-Tetrahydro-1,1′-biphenyl
• 2-Phenylcyclohexene
• Benzene, 1-cyclohexen-1-yl-
• Cyclohex-1-En-1-Ylbenzene
• Cyclohexene, 1-phenyl-
• NSC 403862
• NSC 44834
• 1-Phenyl-1-cyclohexene

1-Phenyl-1-cyclohexene

CAS: 771-98-2

Formula: C₁₂H₁₄

Purity: >95.0%(GC)

Color and Shape: Colorless to Almost colorless clear liquid

Molecular weight: 158.24

Ref: 3B-P1302

1-Phenylcyclohexene, 96%

CAS: 771-98-2

It is used as a pharmaceutical intermediate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as

Formula: C₁₂H₁₄

Purity: 96%

Color and Shape: Liquid, Clear colorless

Molecular weight: 158.24

Ref: 02-B20602

1-Phenyl-1-cyclohexene

CAS: 771-98-2

Formula: C₁₂H₁₄

Purity: 97%

Color and Shape: Liquid

Molecular weight: 158.2396

Ref: IN-DA0032TW

2,3,4,5-Tetrahydro-1,1'-biphenyl

CAS: 771-98-2

2,3,4,5-Tetrahydro-1,1'-biphenyl

Purity: 98%

Molecular weight: 158.24g/mol

Ref: 54-OR80280

1-PHENYL-1-CYCLOHEXENE

CAS: 771-98-2

Formula: C₁₂H₁₄

Purity: 98%

Color and Shape: No data available.

Molecular weight: 158.244

Ref: 10-F513072

1-Phenyl-1-cyclohexene

Controlled Product

CAS: 771-98-2

Applications 1-Phenyl-1-cyclohexene is metabolite of Phencyclidine (P295500), an anesthetic.
References Wong, L.K., et al.L Biomed. Sci. Spec., 2, 204 (1975); Chen, G., et al.: J. Pharmacol. Exp. Ther., 127, 241 (1959); Bailey, K., et al.: J. Pharm. Pharmacol., 28, 713 (1976); Balster, R.L., J. Psychedelic Drugs., 10115 (1978); Johnson, K.M., et al.: Annu. Rev. Pharmacol. Toxicol., 30, 707 (1990)

Formula: C₁₂H₁₄

Color and Shape: Neat

Molecular weight: 158.24

Ref: TR-P319750

1-Phenyl-1-cyclohexene

CAS: 771-98-2

1-Phenyl-1-cyclohexene is a phenolic compound that is synthesized by the cleavage of trifluoroacetic acid. It can be hydrogenated to form cyclohexylbenzene and hydroxylated to form cyclohexanone. 1-Phenyl-1-cyclohexene has been shown to have a locomotor activity in mice, which may be due to its effect on the central nervous system. This compound also reacts with phenol and cyclohexanone to form 1,2,3,4-tetrahydroquinoline and 1,2,3,4-tetrahydropyridine respectively. Kinetic data for this reaction were obtained using the catalyst (palladium) and reaction solution (dimethylformamide). Nitrogen atoms are observed in the reaction mechanism as they bind with oxygen atoms from water molecules in order to produce hydroxide ions. Reaction conditions

Formula: C₁₂H₁₄

Purity: Min. 95%

Molecular weight: 158.24 g/mol

Ref: 3D-AAA77198