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等级
analytical standard
质量水平
蒸汽密度
5.2 (vs air)
蒸汽压
0.06 mmHg ( 20 °C)
方案
≥98% (GC)
保质期
limited shelf life, expiry date on the label
技术
HPLC: suitable
gas chromatography (GC): suitable
折射率
n20/D 1.471 (lit.)
沸点
87-88 °C/6 mmHg (lit.)
密度
0.929 g/mL at 25 °C (lit.)
应用
cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care
包装形式
neat
储存温度
2-8°C
SMILES字符串
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
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一般描述
Dihydrocarvone, an oxygenated monoterpene, is used in the synthesis of several products, including chiral bicyclic phenols, hydroxy ketone 7, lucinone, etc. Dihydrocarvone is also a potential insect repellent known to be effective against the rice weevil Sitophilus oryzae (L), and an inhibitor of bacterial and fungal growth.[1][2][3][4][5]
包装
Bottomless glass bottle. Contents are inside inserted fused cone.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
10 - Combustible liquids
WGK
WGK 2
闪点(°F)
177.8 °F - closed cup
闪点(°C)
81 °C - closed cup
Application of the tandem Stryker reduction--aldol cyclization strategy to the asymmetric synthesis of lucinone
Chiu P, et al.
Tetrahedron Letters, 42(24), 4091-4093 (2001)
(+)-Occidentalol: Absolute Stereostructure and Total Synthesis
Amano Y and Heathcock CH
Canadian Journal of Chemistry, 50(3), 340-345 (1972)
Aromatic annulation: Two new methods for the synthesis of chiral bicyclic phenols
Corey EJ and Palani A
Tetrahedron Letters, 38(14), 2397-2400 (1997)
(R)-(-)-carvone and (1R, 4R)-trans-(+)-dihydrocarvone from poiretia latifolia vogel
Porto C, et al.
Journal of the Brazilian Chemical Society, 21(5), 782-786 (2010)
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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