672599
(R)-(+)-1-(2,4,6-三异丙基苯基)乙醇
≥96.0% (HPLC)
别名:
(R)-Stericol®
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关于此项目
经验公式（希尔记法）:
C17H28O
化学文摘社编号:
分子量:
248.40
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352002
MDL number:
Assay:
≥96.0% (HPLC)
InChI
1S/C17H28O/c1-10(2)14-8-15(11(3)4)17(13(7)18)16(9-14)12(5)6/h8-13,18H,1-7H3/t13-/m1/s1
SMILES string
CC(C)c1cc(C(C)C)c([C@@H](C)O)c(c1)C(C)C
InChI key
VYKPQIIFUMKNLF-CYBMUJFWSA-N
assay
≥96.0% (HPLC)
optical purity
enantiomeric ratio: ≥98:2 (HPLC)
functional group
hydroxyl
storage temp.
2-8°C
Application
Legal Information
Stericol is a registered trademark of Université Joseph Fourier
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
A New Asymmetric Carbon-Carbon Bond Forming Reaction: Four-Component Stereoselective Synthesis of (Z)-4,6-Dihydroxy-3-methylalk-2-enyl Methyl Sulfones This work was supported by the Swiss National Science Foundation.
Narkevitch et al.
Angewandte Chemie (International ed. in English), 39(10), 1806-1808 (2000-08-10)
Hamel, M., et al.
Tetrahedron Asymmetry, 16, 3406-3415 (2005)
Caroline Roche et al.
The Journal of organic chemistry, 70(21), 8352-8363 (2005-10-08)
Three natural pyrrolizidines, (+)-amphorogynines A and D and (+)-retronecine, have been prepared from a common lactam intermediate. This central compound, in turn, was synthesized in diastereomerically enriched form through a highly selective [2 + 2]-cycloaddition of dichloroketene with a chiral
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