80192-56-9

Basic information

• Product Name: 2,4-DIMETHYL-2,6-HEPTADIEN-1-OL
• Synonyms: 2,4-DIMETHYL-2,6-HEPTADIEN-1-OL;2,4-dimethylhepta-2,6-dien-1-ol;2,4-DIMETHYL-2,6-HEPTADIEN-1-OL, 96%, MIXTURE OF ISOMERS;2,4-Mimethyl-2,6-heptadien-1-ol;2,6-Heptadien-1-ol, 2,4-dimethyl-;2,4-Dimethyl-2,6-heptadien-1-ol,mixture of isomers;2,4-Dimethyl-2,6-heptadien-1-ol,99%
• CAS NO: 80192-56-9
• Molecular Formula: C₉H₁₆O
• Molecular Weight: 140.22
• EINECS: 279-418-2
• Mol File: 80192-56-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 86 °C10 mm Hg(lit.)
• Flash Point: 173 °F
• Appearance: /
• Density: 0.865 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.143mmHg at 25°C
• Refractive Index: n20/D 1.464(lit.)
• PKA: 14.71±0.10(Predicted)
• CAS DataBase Reference: 2,4-DIMETHYL-2,6-HEPTADIEN-1-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-DIMETHYL-2,6-HEPTADIEN-1-OL(80192-56-9)
• EPA Substance Registry System: 2,4-DIMETHYL-2,6-HEPTADIEN-1-OL(80192-56-9)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• WGK Germany: 3
• Hazardous Substances Data: 80192-56-9(Hazardous Substances Data)

Usage

Chemical Properties

clear colorless to pale yellow liquid

InChI:InChI=1/C9H16O/c1-4-5-8(2)6-9(3)7-10/h4,6,8,10H,1,5,7H2,2-3H3/b9-6+/t8-/m0/s1

Upstream product

• 85136-08-9 2,4-dimethyl-2,6-heptadienal 

Relevant articles and documents

Highly chemoselective catalytic hydrogenation of unsaturated ketones and aldehydes to unsaturated alcohols using phosphine-stabilized copper(I) hydride complexes

A base metal hydrogenation catalyst composed of the phenyldimethylphosphine-stabilized copper(I) hydride complex provides for the highly chemoselective hydrogenation of unsaturated ketones and aldehydes to unsaturated alcohols, including the regioselective 1,2-reduction of α,β- unsaturated ketones and aldehydes to allylic alcohols. The active catalyst can be derived in situ by phosphine exchange using commercial [(Ph3P)CuH]6 or from the reaction of copper(l) chloride, sodium tert-butoxide, and dimethylphenylphosphine under hydrogen. The catalyst derived from 1,1,1- tris(diphenylphosphinomethyl)ethane is mechanistically interesting but less synthetically useful. (C) 2000 Elsevier Science Ltd.