41641-09-2

Basic information

• Product Name: 1-(3-hydroxybut-1-yn-1-yl)-2,2,6-trimethylcyclohexanol
• CAS NO: 41641-09-2
• Molecular Formula: C₁₃H₂₂O₂
• Molecular Weight: 210.3126
• Mol File: 41641-09-2.mol

Chemical Properties

• Boiling Point: 321.1°C at 760 mmHg
• Flash Point: 145.8°C
• Density: 1.02g/cm³
• Vapor Pressure: 2.46E-05mmHg at 25°C
• Refractive Index: 1.509
• CAS DataBase Reference: 1-(3-hydroxybut-1-yn-1-yl)-2,2,6-trimethylcyclohexanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-hydroxybut-1-yn-1-yl)-2,2,6-trimethylcyclohexanol(41641-09-2)
• EPA Substance Registry System: 1-(3-hydroxybut-1-yn-1-yl)-2,2,6-trimethylcyclohexanol(41641-09-2)

Safety Data

• Hazardous Substances Data: 41641-09-2(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1-(3-hydroxybut-1-yn-1-yl)-2,2,6-trimethylcyclohexanol is used as a building block for the synthesis of other organic compounds, which can be further utilized in the development of new drugs. Its unique structure allows for the creation of a variety of molecules with potential therapeutic properties.
Used in Chemical Industry:
In the chemical industry, 1-(3-hydroxybut-1-yn-1-yl)-2,2,6-trimethylcyclohexanol is used as a component in the development of new materials. Its specific properties and reactivity can contribute to the creation of innovative materials with diverse applications, such as in coatings, adhesives, or polymers.

Upstream product

• 2408-37-9 2,2,6-trimethylcyclohexan-1-one 
• 2028-63-9 but-3-yn-2-ol 
• 820-01-9 3-(1-butoxy-ethoxy)-but-1-yne 
• 20013-73-4 2,6,6-trimethylcyclohex-2-en-1-one 
• 41613-59-6 1-ethynyl-2,2,6-trimethyl-1-cyclohexanol 
• 75-07-0 acetaldehyde 

Downstream Products

• 101170-07-4 4-(2,2,6-trimethyl-cyclohexylidene)-but-3-en-2-ol 
• 106950-29-2 optically inactive 1-(3-hydroxy-but-1-en-c-yl)-2,2,6-trimethyl-cyclohexanol 
• 106950-29-2 optically inactive 1-(3-hydroxy-but-1-en-t-yl)-2,2,6-trimethyl-cyclohexanol 
• 53767-45-6 4-(1-hydroxy-2,2,6-trimethyl-cyclohexyl)-but-3-yn-2-one 
• 23726-91-2 beta damascone 
• 468-70-2 Bicyclofarnesic acid 
• 446293-91-0 4-(2,6,6-trimethyl-cyclohex-1-enyl)-butan-2-ol 
• 4211-33-0 (E) 3-Methyl-5-(2,2,6-trimethylcyclohexen-1-yl)-2-pentenoic Acid 
• 236744-59-5 Ethyl 3-Methyl-5-(2,2,6-trimethylcyclohexen-1-yl)-2-pentenoate 
• 17283-81-7 4-(2,6,6-Trimethyl-cyclohex-1-enyl)-butan-2-on 
• 4179-00-4 Methyl (E)-3-methyl-5-(2,6,6-trimethylcyclohexen-1-yl)-2-pentenoate 
• 82462-59-7 4-(1-Hydroxy-2,2,6-trimethylcyclohexyl)-2-butanol 

Relevant articles and documents

Synthesis method of beta-damascenone

The invention provides a synthesis method of beta-damascenone. The synthesis method comprises the following steps: 1) carrying out nucleophilic addition reaction on a compound II and acetylene to generate a compound III; (2) carrying out condensation reaction on the compound III and acetaldehyde to generate a compound IV, and (3) carrying out Meyer-Schureter rearrangement reaction on the compoundIV to obtain a compound V, namely the beta-damascenone.