87625-10-3

Basic information

• Product Name: 4-PENTYLBICYCLOHEXYL-4-ONE
• Synonyms: 4-PENTYLBICYCLOHEXYL-4-ONE;4-Pentyl-[1,1-bi(cyclohexan)]-4-one
• CAS NO: 87625-10-3
• Molecular Formula: C17H30O
• Molecular Weight: 250.42
• Mol File: 87625-10-3.mol

Chemical Properties

• Appearance: /
• Density: 0.926
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-PENTYLBICYCLOHEXYL-4-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-PENTYLBICYCLOHEXYL-4-ONE(87625-10-3)
• EPA Substance Registry System: 4-PENTYLBICYCLOHEXYL-4-ONE(87625-10-3)

Safety Data

• Hazardous Substances Data: 87625-10-3(Hazardous Substances Data)

Usage

Uses

Used in Fragrance and Flavor Industry:
4-PENTYLBICYCLOHEXYL-4-ONE is used as an intermediate in the synthesis of fragrances and flavors, contributing to the creation of unique scents and tastes in various consumer products.
Used in Pharmaceutical Industry:
PBCH is utilized in the production of pharmaceuticals, serving as a key component in the development of new drugs and medicinal compounds.
Used as a Chemical Intermediate:
4-PENTYLBICYCLOHEXYL-4-ONE is used as a chemical intermediate in the manufacture of other organic compounds, playing a crucial role in the synthesis of a wide range of chemical products.
Used in Organic Synthesis:
PBCH has potential applications in the field of organic synthesis, where it can be employed to create new and innovative organic molecules for various purposes.
Used in Material Development:
4-PENTYLBICYCLOHEXYL-4-ONE is also involved in the development of new materials, showcasing its potential in contributing to advancements in material science and technology.

Upstream product

• 110568-39-3 4-(trans-4-Pentylcyclohexyl)-2-cyclohexen-1-on 
• 110568-28-0 trans-4-Pentyl-2-cyclohexen-1-ol 
• 110568-26-8 trans-6-Pentyl-2-cyclohexen-1-ol 
• 82575-69-7 4-(trans-4-n-pentylcyclohexyl)phenol 
• 82575-70-0 trans-4-cyclohexanol 
• 110568-36-0 1-piperidin 
• 95925-58-9 2-(4-Pentylcyclohexyl)acetaldehyd 
• 110568-30-4 (RS)-(1l,2l,3u,4l)-2,3-Epoxy-4-pentylcyclohexanol 
• 98789-91-4 4-n-pentyl-2-cyclohexen-1-one 
• 63606-79-1 6-Pentyl-2-cyclohexen-1-on 
• 110568-32-6 trans-3-(trans-6-Pentyl-2-cyclohexen-1-yloxy)acrylsaeure-methylester 
• 110568-37-1 5-Oxo-2-(4-pentyl-cyclohexyl)-hexanal 
• 110568-33-7 2-(4-Pentyl-2-cyclohexen-1-yl)formylessigsaeure-methylester 
• 110568-34-8 (6-Pentyl-2-cyclohexen-1-yl)vinylether 

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.

Aliphatic Liquid Crystals, 8. - Bi- and Tercyclohexyl Derivatives by Claisen Rearrangement

Claisen rearrangement of the acrylic esters 7 and 21 transfers the configuration of the cyclohexenols trans-2 and trans-17 to the aldehydes 11 and 23.Robinson annelation converts the latter to the title compounds 15a and 27a.The synthetic sequence is desi