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Merck
CN

46208

Supelco

(+)-葑酮

analytical standard

别名:

(+)-1,3,3-三甲基-2-降冰片酮, (1S)-1,3,3-三甲基二环[2.2.1]庚-2-酮

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About This Item

经验公式(希尔记法):
C10H16O
CAS号:
分子量:
152.23
Beilstein:
2206555
EC 号:
MDL编号:
UNSPSC代码:
85151701
PubChem化学物质编号:
NACRES:
NA.24

等级

analytical standard

质量水平

检测方案

≥99.5% (sum of enantiomers, GC)

旋光性

[α]20/D +62±1°, neat

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

折射率

n20/D 1.462

bp

63-65 °C/13 mmHg (lit.)

mp

5-7 °C (lit.)

密度

0.945 g/mL at 20 °C (lit.)

应用

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

格式

neat

SMILES字符串

CC1(C)[C@@H]2CC[C@@](C)(C2)C1=O

InChI

1S/C10H16O/c1-9(2)7-4-5-10(3,6-7)8(9)11/h7H,4-6H2,1-3H3/t7-,10+/m1/s1

InChI key

LHXDLQBQYFFVNW-XCBNKYQSSA-N

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应用

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

其他说明

高纯度 (+)-葑酮;酮官能可以多种方式转化

储存分类代码

10 - Combustible liquids

WGK

WGK 2

闪点(°F)

150.8 °F - closed cup

闪点(°C)

66 °C - closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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分析证书(COA)

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P. Gosselin et al.
Tetrahedron Letters, 31, 3151-3151 (1990)
L.A. Paquette et al.
The Journal of Organic Chemistry, 57, 3965-3965 (1992)
Santiago de la Moya Cerero et al.
The Journal of organic chemistry, 68(4), 1451-1458 (2003-02-15)
Valuable chiral sources of C(10)-substituted camphors and C(10)-substituted fenchones can be straightforwardly obtained by treatment of an appropriate, easily obtainable, camphor- or fenchone-derived 2-methylenenorbornan-1-ol with an electrophilic reagent. The process takes place via a tandem regioselective carbon-carbon double-bond addition/stereocontrolled Wagner-Meerwein
Mitsuo Miyazawa et al.
Biological & pharmaceutical bulletin, 29(12), 2354-2358 (2006-12-05)
The in vitro metabolism of (+)-fenchone was examined in human liver microsomes and recombinant enzymes. Biotransformation of (+)-fenchone was investigated by gas chromatography-mass spectrometry. (+)-Fenchone was found to be oxidized to 6-exo-hydroxyfenchone, 6-endo-hydroxyfenchone and 10-hydroxyfenchone by human liver microsomal P450
Dirk W Lachenmeier et al.
Journal of agricultural and food chemistry, 56(9), 3073-3081 (2008-04-19)
Thirteen samples of authentic absinthe dating from the preban era (i.e., prior to 1915) were analyzed for parameters that were hypothesized as contributing to the toxicity of the spirit, including naturally occurring herbal essences (thujone, pinocamphone, fenchone), methanol, higher alcohols

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