23182
氯甲酸(+)-1-(9-芴)乙酯 溶液
≥18 mM in acetone, derivatization grade (chiral), LiChropur™
别名:
(+)-FLEC 溶液
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关于此项目
经验公式（希尔记法）:
C16H13ClO2
化学文摘社编号:
分子量:
272.73
UNSPSC Code:
41115716
PubChem Substance ID:
NACRES:
NA.22
MDL number:
产品名称
氯甲酸(+)-1-(9-芴)乙酯 溶液, ≥18 mM in acetone, derivatization grade (chiral), LiChropur™
SMILES string
ClC(=O)OC(C1c2c(cccc2)c3c1cccc3)C
InChI
1S/C16H13ClO2/c1-10(19-16(17)18)15-13-8-4-2-6-11(13)12-7-3-5-9-14(12)15/h2-10,15H,1H3
InChI key
SFRVOKMRHPQYGE-UHFFFAOYSA-N
grade
derivatization grade (chiral)
product line
ChiraSelect™
optical purity
enantiomeric ratio: ≥99.0:1.0 (HPLC)
quality
LiChropur™
concentration
≥18 mM in acetone
technique(s)
HPLC: suitable
refractive index
n20/D 1.359
storage temp.
2-8°C
Quality Level
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Application
(+)-FLEC 可用于反相高效液相色谱-荧光检测系统的草铵膦对映选择性分析。
General description
(+)-1-（9-芴基）氯甲酸乙酯 [(+)-FLEC] 是一种手性衍生试剂。有助于分离 α 的对映体-氨基酸，以及有助于采用 HPLC 法测定其光学纯度。
Physical form
溶液，5mg 溶于 1mL 丙酮中
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
Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
target_organs
Central nervous system
supp_hazards
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
1.4 °F
flash_point_c
-17 °C
法规信息
危险化学品
易制毒化学品（3类）
此项目有
Separation of enantiomers of a-hydroxy acids by reversed-phase liquid chromatography after derivatization with 1-(9-fluorenyl) ethyl chloroformate.
Fransson, Bengt, and Ulf Ragnarsson.
Journal of Chromatography A, 827, 31-36 (1998)
Separation of amino acid enantiomers and chiral amines using precolumn derivatization with (+)-1-(9-fluorenyl)ethyl chloroformate and reversed-phase liquid chromatography.
S Einarsson et al.
Analytical chemistry, 59(8), 1191-1195 (1987-04-15)
Yasushi Hori et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 776(2), 191-198 (2002-07-26)
We have developed a new analytical method to quantify the DL-homoalanine-4-yl(methyl)phosphinate (DL-GLUF) enantiomers in biological specimens using a reversed-phase high-performance liquid chromatography system with a fluorescence detection system. The derivatization of DL-GLUF enantiomers with (+)-1-(9-fluorenyl)ethyl chloroformate was carried out under
Identifying the carboxy terminal amino acid of a protein.
T H Akiyama et al.
Methods in molecular biology (Clifton, N.J.), 64, 235-242 (1997-01-01)
Michelle A Camerino et al.
Organic & biomolecular chemistry, 11(16), 2571-2573 (2013-03-14)
An efficient synthesis of the enantiomers of fluorenylethylchloroformate (FLEC) has been achieved that allows the routine application of the reagent for the resolution of chiral amines including unusual amino acids. The utility of the fluorenylethoxycarbonyl (Feoc) group as a chiral
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