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Merck

194654

Sigma-Aldrich

菊醇,顺反异构体混合物

98%

别名:

2,2-二甲基-3-(2-甲基丙烯基)环丙甲醇, 野菊花醇

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About This Item

线性分子式:
(CH3)2C3H2[CH=C(CH3)2]CH2OH
CAS号:
分子量:
154.25
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:

方案

98%

折射率

n20/D 1.475 (lit.)

沸点

66-69 °C/0.07 mmHg (lit.)

密度

0.888 g/mL at 25 °C (lit.)

SMILES字符串

C\C(C)=C\C1C(CO)C1(C)C

InChI

1S/C10H18O/c1-7(2)5-8-9(6-11)10(8,3)4/h5,8-9,11H,6H2,1-4H3

InChI key

HIPIENNKVJCMAP-UHFFFAOYSA-N

一般描述

Oxidation of chrysanthemyl alcohol in the presence of [RuO4]2- yields chrysantheniic acid[1].

应用

Chrysanthemyl alcohol was used in the determination of position of double bonds in various terepenes and branched chain compounds[2].

象形图

Environment

危险声明

预防措施声明

危险分类

Aquatic Chronic 2

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

185.0 °F - closed cup

闪点(°C)

85 °C - closed cup


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A B Attygalle et al.
Analytical chemistry, 65(18), 2528-2533 (1993-09-15)
The electron-impact mass spectra of alpha, beta-bis(methylthio) derivatives of certain terpenes and other compounds with branched alkenyl groups contain diagnostic peaks that can be used for locating the position of the double bond in the parent compound. In contrast to
Oxo complexes of ruthenium (VI) and (VII) as organic oxidants.
Green G, et al.
Journal of the Chemical Society. Perkin Transactions 1, 681-686 (1984)
L Y Mou et al.
Journal of Asian natural products research, 3(2), 103-116 (2001-06-16)
Chrysanthemol (1), a trans-eudesmane type sesquiterpene from Chrysanthemum indicum L., possesses certain anti-inflammatory activity. Its total synthesis was approached from two alternative routes and finally accomplished in ten steps from R-(+)-carvone via alpha-eudesmol (10) as the key intermediate. The overall
[Studies on the chemical constituents of Chrysanthemum indicum L].
D Q Yu et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 22(11), 837-840 (1987-11-01)
Gas chromatographic determination of racemic cis- and trans-chrysanthemols and their potential aldehyde and carboxylic acid microbial metabolites.
M Miski et al.
Journal of chromatography, 437(2), 436-441 (1988-03-25)

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