(Z)-1-methoxy-3,7-dimethylocta-2,6-diene

  • CasNo:2565-83-5
  • purity:99%
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Details

Perfect Factory Offer Excellent quality (Z)-1-methoxy-3,7-dimethylocta-2,6-diene 2565-83-5 with Safe Shipping

  • Molecular Formula: C11H20 O
  • Molecular Weight: 168.279
  • Vapor Pressure: 0.169mmHg at 25°C 
  • Boiling Point: 220.3°Cat760mmHg 
  • Flash Point: 73.5°C 
  • PSA: 9.23000 
  • Density: 0.827g/cm3 
  • LogP: 3.32550 

(Z)-1-methoxy-3,7-dimethylocta-2,6-diene(Cas 2565-83-5) Usage

General Description

(Z)-1-methoxy-3,7-dimethylocta-2,6-diene, also known as myrcene, is a natural organic compound found in the essential oils of various plants, including cannabis, hops, and bay. It is a volatile liquid with a fruity and earthy aroma, and is commonly used in the fragrance and flavor industries. Myrcene has been found to have sedative, analgesic, and anti-inflammatory properties, and is also known to enhance the effects of THC, the psychoactive compound in cannabis. Additionally, myrcene has been studied for its potential as an antitumor and antimutagenic agent. Overall, myrcene is a versatile and bioactive compound with various potential applications in medicine and industry.

InChI:InChI=1/C11H20O/c1-10(2)6-5-7-11(3)8-9-12-4/h6,8H,5,7,9H2,1-4H3/b11-8-

2565-83-5 Relevant articles

Synergic actions of BEA-type zeolites and ultrasonic irradiation in conversion of geraniol

Ramishvili, Ts.,Tsitsishvili,Ivanova,Kokiashvili,Bukia,Kurtsikidze

, p. 438 - 444 (2019)

The geraniol conversion reaction was ini...

Organometallic derivatives of natural products: Dicobalt hexacarbonyl complexes of geranyl-alkynes

Moore, Angela,Ostermann, Johannes,Ortin, Yannick,McGlinchey, Michael J.

, p. 7881 - 7888 (2016/09/12)

Treatment of methyl geranyl ether with d...

Bis(phosphine)cobalt dialkyl complexes for directed catalytic alkene hydrogenation

Friedfeld, Max R.,Margulieux, Grant W.,Schaefer, Brian A.,Chirik, Paul J.

supporting information, p. 13178 - 13181 (2015/03/30)

Planar, low-spin cobalt(II) dialkyl comp...

Hydroxy-group effect on the regioselectivity in a photochemical oxetane formation reaction (the Paterno-Buechi Reaction) of geraniol derivatives

Hisamoto, Ken,Hiraga, Yoshikazu,Abe, Manabu

experimental part, p. 1469 - 1473 (2012/06/18)

The Paterno-Buechi (PB) reaction of gera...

2565-83-5 Process route

methanol
67-56-1

methanol

3,7-dimethylocta-1,6-dien-3-ol
78-70-6

3,7-dimethylocta-1,6-dien-3-ol

3-methoxy-3,7-dimethyl-1,6-octadiene
60763-44-2

3-methoxy-3,7-dimethyl-1,6-octadiene

geraniol methyl ether
2565-83-5,72152-72-8,2565-82-4

geraniol methyl ether

(2Z)-1-methoxy-3,7-dimethylocta-2,6-diene
2565-83-5

(2Z)-1-methoxy-3,7-dimethylocta-2,6-diene

Conditions
Conditions Yield
With ruthenium trichloride;
47%
22%
12%
methanol
67-56-1

methanol

3,7-dimethylocta-1,6-dien-3-ol
78-70-6

3,7-dimethylocta-1,6-dien-3-ol

3-methoxy-3,7-dimethyl-1,6-octadiene
60763-44-2

3-methoxy-3,7-dimethyl-1,6-octadiene

geraniol methyl ether
2565-83-5,72152-72-8,2565-82-4

geraniol methyl ether

(2Z)-1-methoxy-3,7-dimethylocta-2,6-diene
2565-83-5

(2Z)-1-methoxy-3,7-dimethylocta-2,6-diene

Conditions
Conditions Yield
With ruthenium trichloride;
47%
22%
12%

2565-83-5 Upstream products

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    sodium methylate

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    diazomethane

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    Geraniol

2565-83-5 Downstream products

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    α-Cyclogeraniol-methylether

  • 123-35-3
    123-35-3

    7-methyl-3-methene-1,6-octadiene

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    3,7-dimethyl-2,6-octadienal

  • 494-90-6
    494-90-6

    menthofuran

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