Pharmaceutical

6-METHYL-3,5-HEPTADIEN-2-ONE

  • Chemical Name: 6-METHYL-3,5-HEPTADIEN-2-ONE
  • CAS: 1604-28-0
  • Purity: 99%
Inquiry

Purity 99% Min 6-METHYL-3,5-HEPTADIEN-2-ONE 1604-28-0 Spot Supply with Safe Transportation

  • Molecular Formula:C8H12O
  • Molecular Weight:124.183
  • Vapor Pressure:0.464mmHg at 25°C 
  • Refractive Index:1.5340 
  • Boiling Point:193.45 °C at 760 mmHg 
  • Flash Point:68.582 °C 
  • PSA:17.07000 
  • Density:0.858 g/cm3 
  • LogP:2.09780 

6-METHYL-3,5-HEPTADIEN-2-ONE(Cas 1604-28-0) Usage

Preparation

By reacting 2-methylbuten-2-al with acetone in the presence of sodium ethylate or sodium hydroxide; by pyrolysis of tertiary acetylenic carbinyl acetoacetates in the presence of an acid catalyst.

Aroma threshold values

Detection: 375 ppb

Taste threshold values

Taste characteristics at 30 ppm: green and sweet with a brown, herbal aftertaste.

InChI:InChI=1/C8H12O/c1-7(2)5-4-6-8(3)9/h4-6H,1-3H3/b6-4-

1604-28-0 Relevant articles

Method for synthesizing methyl heptenone from methyl butynol

-

Page/Page column 7-8; 11-12, (2020/05/02)

The invention provides a method for synt...

Method for synthesizing alpha,gamma-unsaturated dienone from propargyl alcohol and catalyst system used for method

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, (2019/04/10)

The invention discloses a method for syn...

Palladium-Catalyzed Cleavage of α-Allenylic Aryl Ether toward Pyrazolemethylene-Substituted Phosphinyl Allenes and Their Transformations via Alkenyl C-P(O) Cleavage

Zhu, Jie,Mao, Mao,Ji, Huan-Jing,Xu, Jiang-Yan,Wu, Lei

supporting information, p. 1946 - 1949 (2017/04/28)

A palladium-catalyzed two-component coup...

Gold-catalyzed cycloisomerization of cyclopropyl alkynyl acetates: A versatile approach to 5-, 6-, and 7-membered carbocycles

Zou, Yue,Garayalde, David,Wang, Quanrui,Nevado, Cristina,Goeke, Andreas,Ito, Yoshihiko

supporting information; experimental part, p. 10110 - 10113 (2009/05/30)

Nonclassical chirality transfer? Dependi...

1604-28-0 Process route

2-methyl-but-3-yn-2-ol
115-19-5

2-methyl-but-3-yn-2-ol

1-methyl-4-isopropenylbenzene
1195-32-0

1-methyl-4-isopropenylbenzene

3,3-dimethyl acrylaldehyde
107-86-8

3,3-dimethyl acrylaldehyde

6-methylhepta-3,5-dien-2-one
16647-04-4,29178-96-9,1604-28-0

6-methylhepta-3,5-dien-2-one

p-cymene-8-ol
1197-01-9

p-cymene-8-ol

4,6,6-trimethyl-1,3-cyclohexadiene-1-carboxaldehyde
41793-01-5

4,6,6-trimethyl-1,3-cyclohexadiene-1-carboxaldehyde

Conditions
Conditions Yield
polyvanadioorganosiloxane (3.1percent V); In xylene; at 150 - 160 ℃; for 6h; Mechanism; Rate constant; Product distribution;
62 % Chromat.
6 % Turnov.
4%
2-ethoxyprop-1-ene
926-66-9

2-ethoxyprop-1-ene

2-methyl-but-3-yn-2-ol
115-19-5

2-methyl-but-3-yn-2-ol

6-methylhepta-3,5-dien-2-one
16647-04-4,29178-96-9,1604-28-0

6-methylhepta-3,5-dien-2-one

6-methyl-hepta-4,5-dien-2-one
16647-01-1

6-methyl-hepta-4,5-dien-2-one

Conditions
Conditions Yield
With zinc(II) chloride; at 70 ℃; for 1h; under 15001.5 Torr; Reagent/catalyst; Pressure; Temperature; Overall yield = 63.197 g; Autoclave; Inert atmosphere;

1604-28-0 Upstream products

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    4-methyleneoxetan-2-one

  • 115-19-5
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    1-diethylamino-1-buten-3-one

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    2-methylpropen-1-ylmagnesium bromide

1604-28-0 Downstream products

  • 72345-84-7
    72345-84-7

    (+/-)-β-curcumene

  • 792856-38-3
    792856-38-3

    6-Methyl-2-p-tolyl-3,5-heptadien-2-ol

  • 4630-06-2
    4630-06-2

    6-methylhept-5-en-2-ol

  • 928-68-7
    928-68-7

    6-methylheptan-2-one

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