83811-73-8

Basic information

• Product Name: (4-PHENYLCYCLOHEXYL)METHANOL
• Synonyms: (4-PHENYLCYCLOHEXYL)METHANOL
• CAS NO: 83811-73-8
• Molecular Formula: C₁₃H₁₈O
• Molecular Weight: 190.28142
• Mol File: 83811-73-8.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: (4-PHENYLCYCLOHEXYL)METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (4-PHENYLCYCLOHEXYL)METHANOL(83811-73-8)
• EPA Substance Registry System: (4-PHENYLCYCLOHEXYL)METHANOL(83811-73-8)

Safety Data

• Hazardous Substances Data: 83811-73-8(Hazardous Substances Data)

Usage

General Description

(4-Phenylcyclohexyl)methanol, also known as PCP alcohol, is a chemical compound that is commonly used as a fragrance ingredient in perfumes and personal care products. It is a white crystalline solid with a floral, woody odor. PCP alcohol is classified as a fragrance allergen and is known to cause skin sensitization in some individuals. It is used in small concentrations in fragrances to impart a warm and floral scent. However, it is important to note that PCP alcohol can cause irritation and allergic reactions in sensitive individuals, and proper safety precautions should be taken when handling and using products containing this chemical.

Upstream product

• 36296-69-2 trans-4-phenylcyclohexanecarboxylic acid methyl ester 
• 497-19-8 sodium carbonate 
• 87143-17-7 4-phenyl-1-methylenecyclohexane 
• 4894-75-1 1-phenyl-4-cyclohexanone 
• 142-82-5 n-heptane 
• 143287-94-9 1,2,3,6-tetrahydro-[1,1'-biphenyl]-4-carboxylic acid 
• 22748-63-6 1,2,3,6-tetrahydro-[1,1′-biphenyl]-4-carbonitrile 
• 873949-18-9 ethyl 4-phenyl-1-cyclohexenecarboxylate 

Downstream Products

• 87090-92-4 ((1r,4r)-4-phenylcyclohexyl)methyl 4-methylbenzenesulfonate 
• 1466-73-5 trans-4-phenylcyclohexanecarboxylic acid 
• 56288-51-8 (1s,4s)-4-phenylcyclohexane-1-carboxylic acid 

Relevant articles and documents

Functional Group Interconversion of Alkylidenemalononitriles to Primary Alcohols by a Cooperative Redox Operation

Functional group interconversions are essential chemical processes enabling synthesis. In this report, we describe a strategy to convert alkylidenemalononitriles into primary alcohols in one step. The reaction relies on a choreographed redox process invol

First structure-activity relationship study on dopamine D3 receptor agents with N-[4-(4-Arylpiperazin-1-yl)butyl]-arylcarboxamide structure

Structure-affinity relationships of N-[4-(4-arylpiperazin-1-yl)butyl] arylcarboxamides as D3 receptor ligands have been well characterized but not structure-activity relationships. In a first attempt to clarify this issue, seven 1-(2,3-dichloro

Novel succinate derivative compounds useful as cysteine protease inhibitors

Disclosed are novel succinate derivative compounds of the formula (I)/(Ia): wherein R1, R2, R3, R4, R5, R6, R7, X and A are defined herein. The compounds are useful as inhibitors of cysteine proteases. Also disclosed are methods of using and methods of making such compounds.