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Merck
모든 사진(1)

문서

713937

Sigma-Aldrich

(1S,2S)-trans-1,2-Dihydro-1,2-naphthalenediol

≥96.0% (HPLC)

동의어(들):

(1S-trans)-1,2-Dihydro-1,2-dihydroxynaphthalene

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About This Item

실험식(Hill 표기법):
C10H10O2
CAS Number:
Molecular Weight:
162.19
Beilstein:
1909467
MDL number:
UNSPSC 코드:
12352002
PubChem Substance ID:

분석

≥96.0% (HPLC)

광학 순도

enantiomeric excess: ≥97.0%

저장 온도

2-8°C

SMILES string

O[C@H]1C=Cc2ccccc2[C@@H]1O

InChI

1S/C10H10O2/c11-9-6-5-7-3-1-2-4-8(7)10(9)12/h1-6,9-12H/t9-,10-/m0/s1

InChI key

QPUHWUSUBHNZCG-UWVGGRQHSA-N

포장

Bottomless glass bottle. Contents are inside inserted fused cone.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


시험 성적서(COA)

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문서 라이브러리 방문

Angela M McIver et al.
Biotechnology progress, 24(3), 593-598 (2008-05-13)
The selective oxidation of aryl substrates to chiral cis-1,2-dihydrodiols is an industrially important reaction for the production of intermediates that can be used to produce fine chemicals, pharmaceuticals, and many other bioactive natural products. More specifically, the oxidation of naphthalene
R E Parales et al.
Journal of bacteriology, 180(9), 2337-2344 (1998-05-09)
Bacterial three-component dioxygenase systems consist of reductase and ferredoxin components which transfer electrons from NAD(P)H to a terminal oxygenase. In most cases, the oxygenase consists of two different subunits (alpha and beta). To assess the contributions of the alpha and
Gabriela Chilom et al.
Chemosphere, 56(9), 853-860 (2004-07-21)
The formation of bound residues by naphthalene and its metabolite, cis-naphthalene-1,2-dihydrodiol, in a sediment (1% OC), a silty loam soil (2.9% OC) and a peat (26% OC) was examined. The experiments were carried out under both sterile and nonsterile conditions
N A Leneva et al.
Biochemistry. Biokhimiia, 75(5), 562-569 (2010-07-17)
The ability of Pseudomonas fluorescens 26K strain to utilize naphthalene at concentrations up to 600 mg/liter as the sole source of carbon and energy in mineral liquid media was shown. Using HPLC, TLC, and mass-spectrometry, the intermediates of naphthalene transformation
S Sato et al.
Experimental eye research, 68(5), 601-608 (1999-05-18)
The effects of aldose reductase inhibitors on lens protein modifications induced by naphthalene-1,2-dihydrodiol were investigated in vitro to confirm the role of aldose reductase on naphthalene cataract formation. HPLC analysis of naphthalene-1, 2-dihydrodiol incubated with aldose reductase and NAD+indicated the

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