65132-43-6

Basic information

• Product Name: P-(TRANS-4-HYDROXYCYCLOHEXYL)PHENOL
• Synonyms: P-(TRANS-4-HYDROXYCYCLOHEXYL)PHENOL;4-(TRANS-4'-HYDROXYCYCLOHEXYL)-PHENOL
• CAS NO: 65132-43-6
• Molecular Formula: C₁₂H₁₆O₂
• Molecular Weight: 192.25
• Mol File: 65132-43-6.mol
• Article Data: 5

Chemical Properties

• Melting Point: 222.5-223.5 °C(Solv: ethyl acetate (141-78-6))
• Boiling Point: 357.5±42.0 °C(Predicted)
• Appearance: /
• Density: 1.157±0.06 g/cm3(Predicted)
• PKA: 10.21±0.30(Predicted)
• CAS DataBase Reference: P-(TRANS-4-HYDROXYCYCLOHEXYL)PHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: P-(TRANS-4-HYDROXYCYCLOHEXYL)PHENOL(65132-43-6)
• EPA Substance Registry System: P-(TRANS-4-HYDROXYCYCLOHEXYL)PHENOL(65132-43-6)

Safety Data

• Hazardous Substances Data: 65132-43-6(Hazardous Substances Data)

Usage

General Description

P-(trans-4-hydroxycyclohexyl)phenol is a chemical substance with the molecular formula C12H16O2. It is commonly used as an ultraviolet (UV) filter in sunscreens and other skincare products to protect the skin from harmful UV rays. This chemical compound is known for its ability to absorb and dissipate UV radiation, thereby preventing it from causing damage to the skin. P-(trans-4-hydroxycyclohexyl)phenol is also used as an antioxidant in various cosmetic and personal care products, where it helps to prevent the degradation of other ingredients and extend the shelf life of the product. Additionally, it has anti-inflammatory and soothing properties, making it beneficial for sensitive or irritated skin. Despite its beneficial properties, it is important to use products containing this chemical with caution and in accordance with usage guidelines to avoid any potential adverse effects.

Upstream product

• 92-88-6 4,4'-Dihydroxybiphenyl 
• 105640-07-1 4-(4-hydroxyphenyl)cyclohexan-1-one 
• 5309-16-0 4-(4-methoxyphenyl)cyclohexanone 
• 37810-35-8 4-(4-methoxyphenyl)cyclohexanol 

Downstream Products

• 216880-00-1 trans-4-(4-allyloxyphenyl)cyclohexanol 
• 1239310-97-4 trans-{4-[4-(5-benzyl[1.3.4]thiadiazol-2-ylcarbamoyl)phenyl]cyclohexyloxy}acetic acid 
• 1239311-02-4 tert-butyl trans-{4-[4-(5-benzyl[1.3.4]thiadiazol-2-ylcarbamoyl)phenyl]-cyclohexyloxy}acetate 
• 1239311-01-3 trans-4-(4-tert-butoxycarbonylmethoxycyclohexyl)benzoic acid 
• 1239311-00-2 tert-butyl trans-[4-(4-trifluoromethanesulfonyloxyphenyl)cyclohexyloxy]acetate 
• 1239310-99-6 tert-butyl trans-[4-(4-hydroxyphenyl)cyclohexyloxy]acetate 
• 1239310-98-5 tert-butyl [trans-4-(4-allyloxyphenyl)cyclohexyloxy]acetate 
• 1268813-68-8 C₂₀H₂₂O₄ 
• 1268813-67-7 trans-4-{4-(2,3-epoxypropoxy)phenyl}cyclohexyl 4-(2,3-epoxypropoxy)benzoate 
• 1268813-66-6 C₁₉H₂₀O₄ 
• 102162-14-1 (1r,4r)-4-(4-(benzyloxy)phenyl)cyclohexan-1-ol 
• 680584-26-3 4-Octyloxy-2-[4-(1,1,3,3-tetramethyl-disiloxanyl)-butoxy]-benzoic acid 4-[4-(4-octyloxy-benzoyloxy)-phenyl]-cyclohexyl ester 
• 680584-25-2 2-But-3-enyloxy-4-octyloxy-benzoic acid 4-[4-(4-octyloxy-benzoyloxy)-phenyl]-cyclohexyl ester 
• 680584-23-0 4-octyloxy-benzoic acid 4-(4-hydroxy-phenyl)-cyclohexyl ester 

Relevant articles and documents

A-C Estrogens as Potent and Selective Estrogen Receptor-Beta Agonists (SERBAs) to Enhance Memory Consolidation under Low-Estrogen Conditions

Estrogen receptor-beta (ERβ) is a drug target for memory consolidation in postmenopausal women. Herein is reported a series of potent and selective ERβ agonists (SERBAs) with in vivo efficacy that are A-C estrogens, lacking the B and D estrogen rings. The

SUBSTITUTED (4'-HYDROXYPHENYL)CYCLOALKANE COMPOUNDS AND USES THEREOF AS SELECTIVE AGONISTS OF THE ESTROGEN RECEPTOR BETA ISOFORM

Disclosed are substituted (4'-hydroxylphenyl)cycloalkane compounds and there use as selective agonists of the estrogen receptor beta isoform (ΕΚβ). The disclosed compounds may be formulated as pharmaceutical compositions and administered to treat diseases

Organic reaction in water. Part 3: A facile method for reduction of aromatic rings using a Raney Ni-Al alloy in dilute aqueous alkaline solution under mild conditions

Reduction of aromatic rings such as phenol, naphthalenes, biphenyls, acenaphthene, and acenaphthylene was smoothly performed using a Raney Ni-Al alloy in dilute aqueous alkaline solution without any organic solvents at 90°C under atmospheric pressure, and the corresponding reduced compounds were obtained in high yields. (C) 2000 Elsevier Science Ltd.