14314-21-7

Basic information

• Product Name: 2-methyl-6-methyleneoct-7-en-4-ol
• Synonyms: Einecs 238-254-1;2-methyl-6-methylideneoct-7-en-4-ol
• CAS NO: 14314-21-7
• Molecular Formula: C₁₀H₁₈O
• Molecular Weight: 154.2493
• EINECS: 238-254-1
• Mol File: 14314-21-7.mol
• Article Data: 30

Chemical Properties

• Melting Point: 82-86℃ (0.8 Torr)
• Boiling Point: 222.2±9.0℃ (760 Torr)
• Flash Point: 83.4±15.0℃
• Appearance: /
• Density: 0.848±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 0.0211mmHg at 25°C
• Refractive Index: 1.4688 (20℃)
• PKA: 15.04±0.20(Predicted)
• CAS DataBase Reference: 2-methyl-6-methyleneoct-7-en-4-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-6-methyleneoct-7-en-4-ol(14314-21-7)
• EPA Substance Registry System: 2-methyl-6-methyleneoct-7-en-4-ol(14314-21-7)

Safety Data

• Hazardous Substances Data: 14314-21-7(Hazardous Substances Data)

Usage

General Description

2-methyl-6-methyleneoct-7-en-4-ol is a chemical compound with a molecular formula of C10H18O. It is a terpene alcohol, also known as myrcenol, that is commonly found in the essential oils of various plants including hops, mango, and lemongrass. It is characterized by its fruity and herbal odor and is often used in the fragrance industry to impart a fresh and citrusy scent to perfumes, soaps, and cosmetics. Additionally, 2-methyl-6-methyleneoct-7-en-4-ol has shown potential anti-inflammatory and anti-cancer properties in some studies, making it a subject of interest in the field of medicinal chemistry.

InChI:InChI=1/C10H18O/c1-5-9(4)7-10(11)6-8(2)3/h5,8,10-11H,1,4,6-7H2,2-3H3

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Relevant articles and documents

Einfache Herstellung von 2-Bromomethyl-1,3-butadien, Ipsenol und Ipsdienol

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A REGIO- AND STEREOCONTROLLED ACCESS TO 2,4-DIENOLS BY AMIDE/ALCOHOLATE-PROMOTED RING-OPENING OF DIHYDRO-PYRANS

3,6-Dihydro-2H-pyrans and other, cyclic or acyclic, homoallyl ethers undergo smooth ring-opening through β-elimination when treated with lithium diisopropylamide in the presence of catalytic amounts of potassium tert-butoxide.

2-DIPROPYLBORYLMETHYL-1,3-BUTADIENE - A NEW REAGENT FOR ISOPRENYLATION. EFFICIENT SYNTHESIS OF IPSENOL AND IPSDIENOL

A simple and convenient method for isoprenylation of carbonyl compounds and ethoxyacetylene using the titled new boron containing "isoprene C-5 synthon" and application of this efficient procedure to the synthesis of ipsenol and ipsdienol are described.

ISOPRENYLATION OF CARBONYL COMPOUNDS, ESTERS, AND ALKOXYACETYLENES WITH 2-DIPROPYLBORYLMETHYL-1,3-BUTADIENE AND THE SYNTHESIS OF IPSENOL AND IPSDIENOL

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Pd-catalyzed cross-coupling of allylsilane-vinylcopper species with aryl and vinyl halides: the first total synthesis of (-)-nomadone

The reaction of allene with a lower order silylcuprate 3 leads to an allylsilane-vinylcopper intermediate 4, which undergoes palladium-catalyzed cross-coupling reaction with both vinyl and aryl halides. The influence of several factors such as the nature

A General Method for the Synthesis of 2-Alkyl Substituted 1,3-Dienes Starting from 2-(Chloromethyl)-3-tosylpropene

The alkylation of the monolithium derivative 5 of 2-(chloromethyl)-3-tosylpropene (1) with bromo- or iodo-methyltrimethylsilane affords the β-silyl sulfone 7, which after nucleophilic substitution of the chlorine atom followed by β-elimination of tosyltrimethylsilane, promoted by tetrabutylammonium fluoride (TBAF), gives 2-substituted conjugated dienes 6 and the outer-ring diene 14.Racemic ipsenol (10b), an aggregation pheromone of the bark beetle Ips paraconfusus Lanier, is prepared.