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Merck
모든 사진(1)

주요 문서

37275

Sigma-Aldrich

(+)-Dihydrocarvone

mixture of isomers

동의어(들):

(2R,5R)-5-Isopropenyl-2-methylcyclohexanone

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크기 선택

25 ML
₩48,923

₩48,923


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보기 변경
25 ML
₩48,923

About This Item

실험식(Hill 표기법):
C10H16O
CAS Number:
Molecular Weight:
152.23
Beilstein:
2044615
EC Number:
MDL number:
UNSPSC 코드:
12352115
PubChem Substance ID:
NACRES:
NA.22

₩48,923


구입 가능 여부는 고객센터에 문의하십시오.

벌크 견적 요청

양식

liquid

광학 활성

[α]20/D +20±2°, neat

구성

n-(+)-dihydrocarvone, ~77%
iso-(+)-dihydrocarvone, ~20%

refractive index

n20/D 1.471

density

0.928 g/mL at 20 °C (lit.)

작용기

ketone

SMILES string

CC1CCC(CC1=O)C(C)=C

InChI

1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h8-9H,1,4-6H2,2-3H3

InChI key

AZOCECCLWFDTAP-UHFFFAOYSA-N

일반 설명

(+)-Dihydrocarvone, a monoterpenoid compound[1] found in caraway oil,[2] is a key building block to synthesize sesquiterpenes.[3] It is generally produced either by the hydrogenation of carvone or oxidation of limonene.[2]

애플리케이션

(+)-Dihydrocarvone may be used in the following processes:
  • Synthesis of dispiro 1,2,4,5-tetraoxanes, which show potent anti-malarial activity.[4]
  • Synthesis of an epoxylactone by oxidation, which can undergo copolymerization with ε-caprolactone to form cross-linked copolymers with shape memory properties.[2]
  • Synthesis of α-Cyperone, a eudesmane type sesquiterpenoid compound with potent insecticidal activity.[5]

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

215.6 °F - closed cup

Flash Point (°C)

102 °C - closed cup

개인 보호 장비

Eyeshields, Gloves


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문서 라이브러리 방문

Dan Jin et al.
Scientific reports, 10(1), 3309-3309 (2020-02-26)
Cannabis research has historically focused on the most prevalent cannabinoids. However, extracts with a broad spectrum of secondary metabolites may have increased efficacy and decreased adverse effects compared to cannabinoids in isolation. Cannabis's complexity contributes to the length and breadth
Oxidized dihydrocarvone as a renewable multifunctional monomer for the synthesis of shape memory polyesters.
Lowe JR, et al.
Biomacromolecules, 10(7), 2003-2008 (2009)
The structure and antimalarial activity of dispiro-1, 2, 4, 5-tetraoxanes derived from (+)-dihydrocarvone.
Dong Y, et al.
Bioorganic & Medicinal Chemistry Letters, 20(22), 6359-6361 (2010)
Insecticidal activity of sesquiterpenes skeleton synthesized by the conventional Robinson annulations reaction on Drosophila melanogaster.
Alarcon J, et al.
Industrial Crops and Products, 42, 268-272 (2013)
A Convenient Procedure for the Preparation of Dihydrocarvone.
Raucher S and Hwang K-J.
Synthetic Communications, 10(2), 133-137 (1980)

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