CAS 15356-74-8|(±)-Dihydroactinidiolide

Introduction：Basic information about CAS 15356-74-8|(±)-Dihydroactinidiolide, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. (±)-Dihydroactinidiolide BiologicalActivity
3. Chemical & Physical Properties
4. Safety Information
5. Synonyms

Common Name	(±)-Dihydroactinidiolide
CAS Number	15356-74-8	Molecular Weight	180.243
Density	1.1±0.1 g/cm3	Boiling Point	296.1±9.0 °C at 760 mmHg
Molecular Formula	C₁₁H₁₆O₂	Melting Point	42-43°
MSDS	/	Flash Point	120.2±16.1 °C

Names

Name	Dihydroactinidiolide
Synonym	More Synonyms

(±)-Dihydroactinidiolide BiologicalActivity

Description	(±)-Dihydroactinidiolide, an important aroma compound of black tea and tobacco, has been isolated from several plants. (±)-Dihydroactinidiolide can be formation from β-Carotene by the treatment of polyphenoloxidase, the lipoxygenase, and the xanthine oxidase[1][2].
Related Catalog	Research Areas >>OthersSignaling Pathways >>Others >>Others
References	[1]. Kaneko H, et, al. The Aroma of Cigar Tobacco. Part I. Isolation of 2-Hydroxy-2,6,6-trimethylcyclohexylidene-1-acetic Acid Lactone (Dihydroactinidiolide) from Ether Extract of Cigar Leaves. Agricultural and Biological Chemistry. 1968 Jou; 32(11): 1337-40. [2]. Bosser A, et, al. A Simple Way to (±)-Dihydroactinidiolide from β-Ionone Related to the Enzymic Co-oxidation of β-Carotene in Aqueous Solution. Biotechnology Progress. 1995 Jou; 11(6): 689-92.

Description

(±)-Dihydroactinidiolide, an important aroma compound of black tea and tobacco, has been isolated from several plants. (±)-Dihydroactinidiolide can be formation from β-Carotene by the treatment of polyphenoloxidase, the lipoxygenase, and the xanthine oxidase[1][2].

Related Catalog

Research Areas >>OthersSignaling Pathways >>Others >>Others

References

[1]. Kaneko H, et, al. The Aroma of Cigar Tobacco. Part I. Isolation of 2-Hydroxy-2,6,6-trimethylcyclohexylidene-1-acetic Acid Lactone (Dihydroactinidiolide) from Ether Extract of Cigar Leaves. Agricultural and Biological Chemistry. 1968 Jou; 32(11): 1337-40.

[2]. Bosser A, et, al. A Simple Way to (±)-Dihydroactinidiolide from β-Ionone Related to the Enzymic Co-oxidation of β-Carotene in Aqueous Solution. Biotechnology Progress. 1995 Jou; 11(6): 689-92.

Chemical & Physical Properties

Density	1.1±0.1 g/cm3
Boiling Point	296.1±9.0 °C at 760 mmHg
Melting Point	42-43°
Molecular Formula	C₁₁H₁₆O₂
Molecular Weight	180.243
Flash Point	120.2±16.1 °C
Exact Mass	180.115036
PSA	26.30000
LogP	2.26
Vapour Pressure	0.0±0.6 mmHg at 25°C
Index of Refraction	1.504
InChIKey	IMKHDCBNRDRUEB-UHFFFAOYSA-N
SMILES	CC1(C)CCCC2(C)OC(=O)C=C12
Storage condition	2-8°C

Safety Information

Hazard Codes	Xi

Synonyms

dihydroactinidiolide

T56 BVO AH&TJ A1 F1 F1

2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-, (S)-

2-Hydroxy-2,6,6-trimethylcyclohexylideneacetic acid γ-lactone

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

2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-, (7aS)-

(±)-(2,6,6,-Trimethyl-2-hydroxycyclohexylidene)acetic acid γ-lactone

4,4,7a-Trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one

4,4,7a-Trimethyl-5,6,7,7a-tetrahydro-1-benzofuran-2(4H)-one

UNII:BH8469LVA9

(7aS)-4,4,7a-Trimethyl-5,6,7,7a-tetrahydro-1-benzofuran-2(4H)-one

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

Recommended......