82575-70-0

Basic information

• Product Name: trans-4-(trans-4-Pentylcyclohexyl)cyclohexanol
• Synonyms: trans-4-(trans-4-pentylcyclohexyl)cyclohexanol;Trans-4-(Trans-4-Pentylcyclohexyl)Cyclohexanol,5HheC18H32O;trans-4-n-pentylcyclohexylcyclohexane-4'-carboxylicalcohol;Trans-4-n-Phentylcyclohexyl Cyclohexane-4'-Carboxylc Alcohol;4-TRANS-N-AMYL-CYCLOHEXYLCYCLOHEXANOL;5HHE;4'-Pentyl- (trans,trans)- [1,1'-Bicyclohexyl]-4-methanol;Trans-4-(trans-pentylcyclohexyl)cyclohexanol
• CAS NO: 82575-70-0
• Molecular Formula: C₁₇H₃₂O
• Molecular Weight: 252.44
• Product Categories: Liquid Crystal intermediates
• Mol File: 82575-70-0.mol
• Article Data: 2

Chemical Properties

• Melting Point: 126 °C
• Boiling Point: 342.6±10.0 °C(Predicted)
• Appearance: /
• Density: 0.932±0.06 g/cm3(Predicted)
• Refractive Index: 1.489
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 15.29±0.40(Predicted)
• CAS DataBase Reference: trans-4-(trans-4-Pentylcyclohexyl)cyclohexanol(CAS DataBase Reference)
• NIST Chemistry Reference: trans-4-(trans-4-Pentylcyclohexyl)cyclohexanol(82575-70-0)
• EPA Substance Registry System: trans-4-(trans-4-Pentylcyclohexyl)cyclohexanol(82575-70-0)

Safety Data

• Hazardous Substances Data: 82575-70-0(Hazardous Substances Data)

Usage

Chemical Properties

Milky white liquid

Uses

Intermediates of Liquid Crystals

InChI:InChI=1/C17H32O/c1-2-3-4-5-14-6-8-15(9-7-14)16-10-12-17(18)13-11-16/h14-18H,2-13H2,1H3/t14-,15-,16?,17-

Upstream product

• 82575-69-7 4-(trans-4-n-pentylcyclohexyl)phenol 

Downstream Products

• 71458-06-5 trans-4-propyl-1-(hydroxymethyl)cyclohexane 
• 84868-02-0 4-(trans-4-n-pentylcyclohexyl)cyclohexanone 

Relevant articles and documents

Method for catalytically synthesizing 4-(trans-4-alkylcyclohexyl) cyclohexanone

The invention provides a method for catalytically synthesizing 4-(trans-4-alkylcyclohexyl) cyclohexanone, which comprises the following steps: by taking trans-4-alkylcyclohexyl phenol as a raw material, carrying out catalytic hydrogenation to obtain trans-4-(trans-4-alkylcyclohexyl) cyclohexanol, and then, oxidizing the trans-4-(trans-4-alkylcyclohexyl) cyclohexanol with an oxidizing agent under the catalytic action of piperidine nitroxide free radicals to obtain 4-(trans-4-alkyl cyclohexyl) cyclohexanone. According to the synthesis method, piperidine nitroxide free radicals containing substituent groups are used as the catalyst, compared with a TEMPO catalyst, the production cost is reduced, cost economy is achieved, meanwhile, the problem that TEMPO is difficult to separate and causes pollution easily is solved, and the synthesis method is suitable for actual industrial production.