1-(2,6,6-trimethyl-1-cyclohexen-1-yl)butane-1,3-dione

  • Name: 1-(2,6,6-trimethyl-1-cyclohexen-1-yl)butane-1,3-dione
  • CAS: 39900-12-4
  • Purity: 99%
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Details

Chinese Factory Supply Wholesale 1-(2,6,6-trimethyl-1-cyclohexen-1-yl)butane-1,3-dione 39900-12-4 with Cheap Price

  • Molecular Formula: C13H20 O2
  • Molecular Weight: 208.301
  • Vapor Pressure: 0.00133mmHg at 25°C 
  • Boiling Point: 297.7°C at 760 mmHg 
  • PKA: 9.79±0.40(Predicted) 
  • Flash Point: 111.1°C 
  • PSA: 34.14000 
  • Density: 0.966g/cm3 
  • LogP: 3.06120 

1-(2,6,6-trimethyl-1-cyclohexen-1-yl)butane-1,3-dione(Cas 39900-12-4) Usage

General Description

1-(2,6,6-trimethyl-1-cyclohexen-1-yl)butane-1,3-dione, also known as α-Ionone, is a chemical compound commonly found in natural sources such as roses, violets, and jasmine. It is a cyclic compound with a fruity and floral odor commonly used in perfumes and flavorings. α-Ionone is also used in the production of vitamin A and as a precursor to the synthesis of other chemical compounds. It is considered safe for use in food and cosmetic products and has been approved by regulatory agencies for such applications. Additionally, α-Ionone has potential anti-inflammatory and antioxidant properties, making it of interest for further research in the fields of pharmaceuticals and skincare.

InChI:InChI=1/C13H20O2/c1-9-6-5-7-13(3,4)12(9)11(15)8-10(2)14/h5-8H2,1-4H3

39900-12-4 Relevant articles

1 - (2, 6, 6 - trimethyl - cyclohexenyl) - 2 - butene - 1 - ketone

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Paragraph 0092; 0127; 0128; 0130; 0131; 0133; 0134, (2017/08/25)

The invention provides a 1-(2,6,6-trimet...

Process for preparing 1-(2,6,6-trimethyl-1,3-cyclohexadien-1-yl)-1,3-butanedione and intermediates

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, (2008/06/13)

Described is a process for preparing an ...

1-(2,6,6-Trimethyl-1,3-cyclohexadien-1-yl)-1,3-butanedione and organoleptic uses thereof

-

, (2008/06/13)

Processes and compositions are described...

Process for the preparation of damascenone derivatives

-

, (2008/06/13)

New alicyclic ketones useful for perfume...

39900-12-4 Process route

ISOXAZOLE
288-14-2

ISOXAZOLE

1-(2,6,6-trimethyl-1-cyclohexenyl)-1,3-butanedione
39900-12-4

1-(2,6,6-trimethyl-1-cyclohexenyl)-1,3-butanedione

Conditions
Conditions Yield
1-(2,6,6-trimethyl-3-cyclohexenyl)-1,3-butanedione

1-(2,6,6-trimethyl-3-cyclohexenyl)-1,3-butanedione

1-(2,6,6-trimethyl-2-cyclohexenyl)-1,3-butanedione
39900-11-3

1-(2,6,6-trimethyl-2-cyclohexenyl)-1,3-butanedione

1-(2,6,6-trimethyl-1-cyclohexenyl)-1,3-butanedione
39900-12-4

1-(2,6,6-trimethyl-1-cyclohexenyl)-1,3-butanedione

Conditions
Conditions Yield
With sodium t-butanolate; In N,N-dimethyl-formamide; at 30 ℃; for 3h; Solvent; Reagent/catalyst; Temperature; Overall yield = 81.1 %;
58 g
88 g

39900-12-4 Upstream products

  • 39190-07-3
    39190-07-3

    2,6,6-trimethyl-1-[3-amino-but-2-en-1-oyl]-cyclohex-1-ene

  • 25915-53-1
    25915-53-1

    2,6,6-trimethyl-3-cyclohexenyl methyl ketone

39900-12-4 Downstream products

  • 39900-16-8
    39900-16-8

    2,6,6-trimethyl-1-[3-hydroxy-butan-1-oyl]-cyclohex-1-ene

  • 52087-89-5
    52087-89-5

    2,6,6-Trimethyl-1-[1,3-dihydroxy-but-1-yl]-cyclohex-1-ene

  • 35044-68-9
    35044-68-9

    1-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-buten-1-one

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