14168-34-4

Basic information

• Product Name: (1E)-3-methyl-1-(2,6,6-trimethylcyclohex-1-en-1-yl)hex-1-en-5-yn-3-ol
• CAS NO: 14168-34-4
• Molecular Formula: C₁₆H₂₄O
• Molecular Weight: 232.3612
• Mol File: 14168-34-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 345.5°C at 760 mmHg
• Flash Point: 326.7°C
• Density: 0.978g/cm³
• Vapor Pressure: 3.84E-06mmHg at 25°C
• Refractive Index: 1.543
• CAS DataBase Reference: (1E)-3-methyl-1-(2,6,6-trimethylcyclohex-1-en-1-yl)hex-1-en-5-yn-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (1E)-3-methyl-1-(2,6,6-trimethylcyclohex-1-en-1-yl)hex-1-en-5-yn-3-ol(14168-34-4)
• EPA Substance Registry System: (1E)-3-methyl-1-(2,6,6-trimethylcyclohex-1-en-1-yl)hex-1-en-5-yn-3-ol(14168-34-4)

Safety Data

• Hazardous Substances Data: 14168-34-4(Hazardous Substances Data)

Usage

Description

(1E)-3-methyl-1-(2,6,6-trimethylcyclohex-1-en-1-yl)hex-1-en-5-yn-3-ol is a chemical compound with the molecular formula C15H24O. It is a long-chain aliphatic alcohol containing a terminal alkyne group and a cyclohexene ring. (1E)-3-methyl-1-(2,6,6-trimethylcyclohex-1-en-1-yl)hex-1-en-5-yn-3-ol is a liquid at room temperature and is insoluble in water but soluble in organic solvents.

Uses

Used in Organic Synthesis:
(1E)-3-methyl-1-(2,6,6-trimethylcyclohex-1-en-1-yl)hex-1-en-5-yn-3-ol is used as a reagent in organic synthesis for the production of various compounds. Its unique structure, including the terminal alkyne group and cyclohexene ring, allows for versatile chemical reactions and the formation of a wide range of products.
Used in Chemical Research:
In the field of chemical research, (1E)-3-methyl-1-(2,6,6-trimethylcyclohex-1-en-1-yl)hex-1-en-5-yn-3-ol serves as an intermediate in the synthesis of complex organic molecules. Its properties and reactivity make it a valuable tool for studying reaction mechanisms and developing new synthetic methods.
The exact uses and applications of (1E)-3-methyl-1-(2,6,6-trimethylcyclohex-1-en-1-yl)hex-1-en-5-yn-3-ol may vary depending on the specific field and industry. Its versatility in organic synthesis and chemical research highlights its potential for further exploration and application in various sectors.

Upstream product

• 79-77-6 4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3-buten-2-one 
• 624-65-7 2-propynyl chloride 

Downstream Products

• 950-51-6 6-(2,6,6-Trimethyl-1-cyclohexenyl)-4-methyl-3,5-hexadienin 
• 94462-31-4 4-methyl-6-(2,6,6-trimethyl-cyclohex-2-enylidene)-hex-4-en-1-yne 
• 74352-13-9 (6E,8E)-1,1-Dimethoxy-3,7-dimethyl-9-(2,6,6-trimethyl-cyclohex-1-enyl)-nona-6,8-dien-4-yn-3-ol 
• 96578-66-4 9-(2,6,6-Trimethylcyclohexen-1-yl)-3,7-dimethyl-3-hydroxy-1,1-dimethoxynona-4,6,8-trien 

Relevant articles and documents

Efficient propargylation of aldehydes and ketones catalyzed by titanocene(III)

We describe a novel method for the propargylation of a wide range of aldehydes and ketones catalyzed by titanocene(III) complexes under mild reaction conditions and compatible with many functional groups. Homopropargylic alcohols are obtained as the sole products even when ketones are used as starting materials, which is unusual in Barbier-type propargylations.