What is the DIHYDROACTINIDIOLIDE?

DIHYDROACTINIDIOLIDE is , while it's Molecular Formula is C 11 H 16 O 2 . Used in Fragrance Industry: DIHYDROACTINIDIOLIDE is used as a fragrance ingredient for its powerful musky or coumarin-like odor, which adds depth and complexity to perfumes and other scented products. Used in Flavor Industry: DIHYDROACTINIDIOLIDE is used as a flavor enhancer for its ability to mimic the taste of certain fruits at their peak of ripeness, providing a natural and authentic flavor profile to various food and beverage products. Used in Cosmetics Industry: DIHYDROACTINIDIOLIDE can be used as an additive in the cosmetics industry, where its unique odor can contribute to the overall sensory experience of products such as lotions, creams, and other personal care items. Used in Pharmaceutical Industry: Although not explicitly mentioned in the provided materials, DIHYDROACTINIDIOLIDE's unique chemical properties and odor profile may have potential applications in the pharmaceutical industry, possibly as a component in the development of new drugs or as a flavoring agent for medications. Further research would be required to explore these possibilities.

What is the CAS number for DIHYDROACTINIDIOLIDE?

The CAS number of DIHYDROACTINIDIOLIDE is 15356-74-8.

What is DIHYDROACTINIDIOLIDE (15356-74-8) used for?

DIHYDROACTINIDIOLIDE, also known as (+/–)-(2,6,6-Trimethyl-2-hydroxycyclohexylidene) acetic acid gamma-lactone, is a chemical compound derived from the photooxidation of carotene-like structures. It is characterized by its powerful musky or coumarin-like odor and is associated with the taste of certain fruits at their peak of ripeness. DIHYDROACTINIDIOLIDE is reportedly present in lemongrass and sweet grass oil.InChI:InChI=1/C11H16O2/c1-10(2)5-4-6-11(3)8(10)7-9(12)13-11/h7H,4-6H2,1-3H3

What is the DIHYDROACTINIDIOLIDE?

DIHYDROACTINIDIOLIDE is , while it's Molecular Formula is C 11 H 16 O 2 . Used in Fragrance Industry: DIHYDROACTINIDIOLIDE is used as a fragrance ingredient for its powerful musky or coumarin-like odor, which adds depth and complexity to perfumes and other scented products. Used in Flavor Industry: DIHYDROACTINIDIOLIDE is used as a flavor enhancer for its ability to mimic the taste of certain fruits at their peak of ripeness, providing a natural and authentic flavor profile to various food and beverage products. Used in Cosmetics Industry: DIHYDROACTINIDIOLIDE can be used as an additive in the cosmetics industry, where its unique odor can contribute to the overall sensory experience of products such as lotions, creams, and other personal care items. Used in Pharmaceutical Industry: Although not explicitly mentioned in the provided materials, DIHYDROACTINIDIOLIDE's unique chemical properties and odor profile may have potential applications in the pharmaceutical industry, possibly as a component in the development of new drugs or as a flavoring agent for medications. Further research would be required to explore these possibilities.

What is the CAS number for DIHYDROACTINIDIOLIDE?

The CAS number of DIHYDROACTINIDIOLIDE is 15356-74-8.

What is DIHYDROACTINIDIOLIDE (15356-74-8) used for?

DIHYDROACTINIDIOLIDE, also known as (+/–)-(2,6,6-Trimethyl-2-hydroxycyclohexylidene) acetic acid gamma-lactone, is a chemical compound derived from the photooxidation of carotene-like structures. It is characterized by its powerful musky or coumarin-like odor and is associated with the taste of certain fruits at their peak of ripeness. DIHYDROACTINIDIOLIDE is reportedly present in lemongrass and sweet grass oil.InChI:InChI=1/C11H16O2/c1-10(2)5-4-6-11(3)8(10)7-9(12)13-11/h7H,4-6H2,1-3H3

Detailed introduction

Factory Sells Best Quality Dihydroactinidiolide 15356-74-8 with ISO standards

Molecular Formula:C₁₁H₁₆O₂
Molecular Weight:180.247
Vapor Pressure:0.00147mmHg at 25°C
Melting Point:42-43°
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

DIHYDROACTINIDIOLIDE(Cas 15356-74-8) Usage

Preparation

Prepared in a patented process by degradation of beta-carotene in the presence of nitrogen and air.

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

15356-74-8 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)

Synthesis of natural products has speede...

AN IMPROVED SYNTHESIS OF (+/-)-DIHYDROACTINIDIOLIDE

Subbaraju, Gottumukkala V.,Manhas, Maghar S.,Bose, Ajay K.

, p. 4871 - 4874 (1991)

An improved synthesis of (+/-)-aeginetol...

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...

15356-74-8 Process route

: 302-79-4
all-trans-retinoic-acid

: 15356-74-8,17092-92-1,19432-05-4,81800-41-1
(+/-)-dihydroactinidiolide

: 79-77-6,14901-07-6
(E)-β-ionone

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

: 129454-99-5,195991-40-3
2E,4E-2-methyl-6-oxo-2,4-heptadienal

: 129454-95-1
4-ethoxyretinoic acid

: 3012-76-8,112018-12-9,129520-10-1,129520-11-2
trans-5,8-epoxy-5,8-dihydroretinoic acid

Conditions

Conditions	Yield
With oxygen; In ethanol; water; at 85.5 ℃; for 8h; under 760 Torr; Product distribution; Kinetics; Thermodynamic data; ΔE(excit.); different ratios of O2, solvent, reaction times and temperatures;

: 472-68-4
(2,6,6-trimethylcyclohex-1-enyl)acetic acid

: 15356-74-8,17092-92-1,19432-05-4,81800-41-1
(+/-)-dihydroactinidiolide

Conditions

Conditions	Yield
With diphenyl diselenide; tetraethylammonium bromide; water; sodium carbonate; In acetonitrile; for 0.6h; Ambient temperature; electrolysis under a constant current 70 mA;	92%