4-(4-Hydroxyphenyl)cyclohexanone

CAS : 105640-07-1

Ref. 3D-FH140342

Informations sur le produit

• Nom: 4-(4-Hydroxyphenyl)cyclohexanone
• Synonymes: 4-(4-Oxocyclohexyl)phenol, 4-(P-hydroxyphenyl)cyclohexanone, Cyclohexanone, 4-(4-hydroxyphenyl)-, Cyclohexanone, 4-(p-hydroxyphenyl)-, Hopck, Labotest-Bb Lt00847424, 4-(4'-hydroxyphenyl)-cyclohexanone, 4-(4-Hydroxyphenyl)-cyclohexanone, 4-(4-Hydroxyphenyl) cyclohexanone, 4-(4′-Hydroxyphenyl)cyclohexanone

Description

4-Hydroxyphenylcyclohexanone (4-HPCH) is a reactive molecule that can be used as a precursor in the synthesis of pharmaceuticals and other organic compounds. 4-HPCH reacts with grignard reagents to form cyclohexanol. It also has hydroxyl groups, which are susceptible to radiation. This reaction is catalyzed by various enzymes, such as sphingosine kinase, and is involved in many physiological functions such as effective dose and cell signaling. The products of this reaction are called supramolecular complexes, which can be formed through the interaction of different molecules or atoms. The main product of this reaction is diazide, which has been shown to inhibit the enzyme acetylcholinesterase in mammals cells. The mechanism for this inhibition is thought to involve the formation of an intermediate complex between 4-HPCH and acetyl choline esterase that stabilizes the active site of the enzyme.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 190.24 g/mol
• Formule: C₁₂H₁₄O₂
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C12H14O2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-2,5-6,10,13H,3-4,7-8H2
• Code InChI: InChIKey=SLJYPZJZQIHNGU-UHFFFAOYSA-N
• SMILES: O=C1CCC(c2ccc(O)cc2)CC1