추천 제품
Quality Level
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 found in caraway oil, is a key building block to synthesize sesquiterpenes. It is generally produced either by the hydrogenation of carvone or oxidation of limonene.
애플리케이션
(+)-Dihydrocarvone may be used in the following processes:
- Synthesis of dispiro 1,2,4,5-tetraoxanes, which show potent anti-malarial activity.
- Synthesis of an epoxylactone by oxidation, which can undergo copolymerization with ε-caprolactone to form cross-linked copolymers with shape memory properties.
- Synthesis of α-Cyperone, a eudesmane type sesquiterpenoid compound with potent insecticidal activity.
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
이미 열람한 고객
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)
Oxidized dihydrocarvone as a renewable multifunctional monomer for the synthesis of shape memory polyesters.
Lowe JR, et al.
Biomacromolecules, 10(7), 2003-2008 (2009)
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
Redife Aslihan Ucar et al.
Food microbiology, 91, 103454-103454 (2020-06-17)
This research determined the concentration of trehalose, xylose and l-citrulline in fresh and fermented cucumbers and their utilization by Lactobacillus pentosus, Lactobacillus plantarum, Lactobacillus brevis and Lactobacillus buchneri. Targeted compounds were measured by HPLC and the ability of the lactobacilli
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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