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Merck

87649

Sigma-Aldrich

(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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About This Item

经验公式(希尔记法):
C10H12O
CAS号:
分子量:
148.20
Beilstein:
2208779
MDL號碼:
分類程式碼代碼:
12352002
PubChem物質ID:
NACRES:
NA.22

等級

puriss.

化驗

≥99.0% (sum of enantiomers, GC)

形狀

crystals

光學活性

[α]20/D +33±1°, c = 2.5% in chloroform

光學純度

enantiomeric ratio: 99:1 (GC)

mp

37-39 °C

SMILES 字串

O[C@H]1CCCc2ccccc12

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

InChI 密鑰

JAAJQSRLGAYGKZ-JTQLQIEISA-N

基因資訊

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象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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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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