09164
(+)-二氢香芹酮，异构体混合物
analytical standard
登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C10H16O
化学文摘社编号:
分子量:
152.23
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
85151701
EC Number:
231-857-0
MDL number:
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
SMILES string
CC1CCC(CC1=O)C(C)=C
grade
analytical standard
vapor density
5.2 (vs air)
vapor pressure
0.06 mmHg ( 20 °C)
assay
≥98% (GC)
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
refractive index
n20/D 1.471 (lit.)
bp
87-88 °C/6 mmHg (lit.)
density
0.929 g/mL at 25 °C (lit.)
application(s)
cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care
format
neat
storage temp.
2-8°C
Quality Level
正在寻找类似产品? 访问 产品对比指南
General description
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.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
177.8 °F - closed cup
flash_point_c
81 °C - closed cup
Aromatic annulation: Two new methods for the synthesis of chiral bicyclic phenols
Corey EJ and Palani A
Tetrahedron Letters, 38(14), 2397-2400 (1997)
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)
A Convenient Procedure for the Preparation of Dihydrocarvone.
Raucher S and Hwang K-J.
Synthetic Communications, 10(2), 133-137 (1980)
(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)
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持