87649
(S)-(+)-1,2,3,4-四氢-1-萘酚
puriss., ≥99.0% (sum of enantiomers, GC)
别名:
(S)-(+)-α-四氢萘酚
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关于此项目
经验公式（希尔记法）:
C10H12O
化学文摘社编号:
分子量:
148.20
UNSPSC Code:
12352002
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2208779
产品名称
(S)-(+)-1,2,3,4-四氢-1-萘酚, puriss., ≥99.0% (sum of enantiomers, GC)
InChI
1S/C10H12O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-2,4,6,10-11H,3,5,7H2/t10-/m0/s1
SMILES string
O[C@H]1CCCc2ccccc12
InChI key
JAAJQSRLGAYGKZ-JTQLQIEISA-N
grade
puriss.
assay
≥99.0% (sum of enantiomers, GC)
form
crystals
optical activity
[α]20/D +33±1°, c = 2.5% in chloroform
optical purity
enantiomeric ratio: 99:1 (GC)
mp
37-39 °C
Gene Information
human ... UGT2B17(7367), UGT2B7(7364)
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Urmi Dhagat et al.
Bioorganic & medicinal chemistry letters, 20(17), 5274-5276 (2010-07-27)
A comparison of the structures and kinetic properties of human 20alpha-hydroxysteroid dehydrogenase (AKR1C1) and its mutant enzymes (Leu308Val and Leu308Ala) indicates that Leu308 is a selectivity determinant for substrate binding. While the Leu308Val mutation improved the catalytic efficiency (k(cat)/K(m)) of
Ingo Bichlmaier et al.
Journal of medicinal chemistry, 49(5), 1818-1827 (2006-03-03)
A set of 28 enantiomers comprising rigid and flexible secondary alcohols was synthesized by the asymmetric Corey-Bakshi-Shibata reduction. The enantiomerically pure alcohols were subjected to enzymatic glucuronidation assays employing the human UDP-glucuronosyltransferases (UGTs) 2B7 and 2B17. Both UGTs displayed high
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