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线性分子式:
C10H13O3Cl
化学文摘社编号:
分子量:
216.66
UNSPSC Code:
23151817
NACRES:
NA.22
PubChem Substance ID:
EC Number:
254-552-4
Beilstein/REAXYS Number:
3590860
MDL number:
Assay:
≥98.0% (AT)
≥98.0%
≥98.0%
Form:
solid
产品名称
(1S)-(-)-莰烷酰氯, derivatization grade (chiral), LiChropur™, ≥98.0%
InChI key
PAXWODJTHKJQDZ-VHSXEESVSA-N
InChI
1S/C10H13ClO3/c1-8(2)9(3)4-5-10(8,6(11)12)14-7(9)13/h4-5H2,1-3H3/t9-,10+/m0/s1
SMILES string
CC1(C)[C@@]2(C)CC[C@@]1(OC2=O)C(Cl)=O
grade
derivatization grade (chiral)
product line
ChiraSelect™
assay
≥98.0% (AT)
≥98.0%
form
solid
optical activity
[α]20/D −18±1°, c = 2% in carbon tetrachloride
optical purity
enantiomeric ratio: ≥99.5:0.5 (GC)
quality
LiChropur™
technique(s)
HPLC: suitable
mp
67-70 °C
71-73 °C (lit.)
storage temp.
−20°C
Quality Level
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Application
(1S)-(-)-Camphanic chloride may be used in esterification of enantiomers in volatiles releasedf from wheat, in order to determine the proportion of enantiomers and also in quantifying the esters.
General description
(1S)-(-)-Camphanic chloride is a derivatizing agent.
Legal Information
ChiraSelect is a trademark of Sigma-Aldrich Co. LLC
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
A. Haag et al.
Helvetica Chimica Acta, 63, 10-10 (1980)
J.D. Fourneron et al
The Journal of Organic Chemistry, 54, 4686-4686 (1989)
H. Gerlach
Helvetica Chimica Acta, 68, 1815-1815 (1985)
K.D. Ward et al.
Journal of Chromatography A, 478, 169-169 (1989)
Activity of enantiomers of sulcatol on apterae of Rhopalosiphum padi.
Quiroz, A., and H. M. Niemeyer.
Journal of Chemical Ecology, 24, 361-370 (1998)
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