Dihydroactinidiolide

Available forms:Colorless crystal

pd_proNo:352618-30969781-aa19-4408-893c-5c3560e6f52b

pd_productuse:

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Detailed introduction

Manufacturer supply high quality Dihydroactinidiolide 17092-92-1 with GMP standards

  • Molecular Formula:C11H16O2
  • Molecular Weight:180.247
  • Appearance/Colour:Colorless crystal 
  • Vapor Pressure:0.00147mmHg at 25°C 
  • Melting Point:70-71° 
  • Refractive Index:1.504 
  • Boiling Point:296.099 °C at 760 mmHg 
  • Flash Point:120.249 °C 
  • PSA:26.30000 
  • Density:1.058 g/cm3 
  • LogP:2.43840 

(2,6,6-Trimethyl-2-hydroxycyclohexylidene)acetic acid lactone(Cas 17092-92-1) Usage

Biological activity

Dihydroactinidiolide is present in plant leaves and fruits, is a potent plant growth inhibitor, a regulator of gene expression, and is also responsible for light adaptation in Arabidopsis. Dihydroactinidiolide has antioxidant activity, antibacterial activity, anticancer activity and neuroprotection.

Use

Dihydroactinidiolide is an ester organic matter, which can be used as a food flavor.

InChI:InChI=1/C11H16O2/c1-10(2)5-4-6-11(3)8(10)7-9(12)13-11/h7H,4-6H2,1-3H3

17092-92-1 Relevant articles

Dihydroactinidiolide, a natural product against Aβ25-35 induced toxicity in Neuro2a cells: Synthesis, in silico and in vitro studies

Das, Mamali,Prakash, Sengodu,Nayak, Chirasmita,Thangavel, Nandhini,Singh, Sanjeev Kumar,Manisankar, Paramasivam,Devi, Kasi Pandima

, p. 340 - 349 (2018/09/10)

Synthesis of natural products has speede...

β-Carotene autoxidation: Oxygen copolymerization, non-vitamin A products, and immunological activity

Burton, Graham W.,Daroszewski, Janusz,Nickerson, James G.,Johnston, James B.,Mogg, Trevor J.,Nikiforov, Grigory B.

supporting information, p. 305 - 316 (2014/05/06)

Carotenoids are reported to have immunol...

Cu(I)-catalyzed oxidative cyclization of alkynyl oxiranes and oxetanes

Gronnier, Colombe,Kramer, Soren,Odabachian, Yann,Gagosz, Fabien

, p. 828 - 831 (2012/03/07)

In the presence of a Cu(I) catalyst and ...

Total synthesis of (±)-dihydroactinidiolide using selenium-stabilized carbenium ion

Dabdoub, Miguel J.,Silveira, Claudio C.,Lenard?o, Eder J.,Guerrero Jr., Palimécio G.,Viana, Luiz H.,Kawasoko, Cristiane Y.,Baroni, Adriano C.M.

scheme or table, p. 5569 - 5571 (2011/02/24)

A new, short total synthesis of dihydroa...

17092-92-1 Process route

12'-apo-β-caroten-12'-al
1638-05-7

12'-apo-β-caroten-12'-al

(7aR)-5,6,7,7a-tetrahydro-4,4,7a-trimethyl-2(4H)-benzofuranone
17092-92-1

(7aR)-5,6,7,7a-tetrahydro-4,4,7a-trimethyl-2(4H)-benzofuranone

(E)-β-ionone
79-77-6,14901-07-6

(E)-β-ionone

2,6,6-trimethylcyclohex-1-enecarbaldehyde
432-25-7

2,6,6-trimethylcyclohex-1-enecarbaldehyde

5,6-epoxy-trans-β-ionone
36340-49-5

5,6-epoxy-trans-β-ionone

Conditions
Conditions Yield
With dihydrogen peroxide; sodium acetate; In water; at 27 ℃; for 1h; pH=5; Enzymatic reaction;
beta-carotene
7235-40-7

beta-carotene

(7aR)-5,6,7,7a-tetrahydro-4,4,7a-trimethyl-2(4H)-benzofuranone
17092-92-1

(7aR)-5,6,7,7a-tetrahydro-4,4,7a-trimethyl-2(4H)-benzofuranone

2-hydroxy-2,2,6-trimethylcyclohexanone
7500-42-7

2-hydroxy-2,2,6-trimethylcyclohexanone

(E)-β-ionone
79-77-6,14901-07-6

(E)-β-ionone

2,6,6-trimethylcyclohex-1-enecarbaldehyde
432-25-7

2,6,6-trimethylcyclohex-1-enecarbaldehyde

5,6-epoxy-trans-β-ionone
36340-49-5

5,6-epoxy-trans-β-ionone

Conditions
Conditions Yield
With dihydrogen peroxide; sodium acetate; In water; at 27 ℃; for 1h; pH=5; Enzymatic reaction;

17092-92-1 Upstream products

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    16778-27-1

    4,4,7a-trimethylhexahydro-1-benzofuran-2(3H)-one

  • 29951-40-4
    29951-40-4

    (+/-)-aeginetolide

  • 472-66-2
    472-66-2

    (2,6,6-trimethyl-1-cyclohexen-1-yl)acetaldehyde

  • 472-68-4
    472-68-4

    (2,6,6-trimethylcyclohex-1-enyl)acetic acid

17092-92-1 Downstream products

  • 1258783-37-7
    1258783-37-7

    C11H20O2

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