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Merck
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文件

219975

Sigma-Aldrich

5-羟基-1-四氢萘酮

99%

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About This Item

经验公式（希尔记法）:
C10H10O2
CAS号:
28315-93-7
分子量:
162.19
Beilstein:
2437410
EC號碼:
248-958-0
MDL號碼:
MFCD00001693
分類程式碼代碼:
12352100
PubChem物質ID:
24853157
NACRES:
NA.22

化驗

99%

mp

206-209 °C (lit.)

SMILES 字串

Oc1cccc2C(=O)CCCc12

InChI

1S/C10H10O2/c11-9-5-1-3-7-8(9)4-2-6-10(7)12/h1,3,5,11H,2,4,6H2

InChI 密鑰

YPPZCRZRQHFRBH-UHFFFAOYSA-N

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應用

5-Hydroxy-1-tetralone was used:
  • as internal standard during HPLC determination of 4-hydroxymephenytoin (4-OH-M) in human urine
  • as fluorescent labeling reagent during microdetection of glycosphingolipid on TLC plates
  • in synthesis of 1,2,3,4-tetrahydro-5H-1-benzazepine-quinone derivatives
  • in synthesis of new chiral oxathiane

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

Eyeshields, Gloves, type N95 (US)

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Studies on Quinones. Part 22.'Synthesis of 1-Benzazepine-6, 9-Quinone Derivatives.
Valderrama JA, et al.
Synthetic Communications, 22(4), 629-640 (1992)
K Watanabe et al.
Journal of lipid research, 36(8), 1848-1855 (1995-08-01)
A microdetection system for glycosphingolipid analysis has been developed using 5-hydroxy-1-tetralone as the fluorescent labeling reagent. The reagents in H2SO4 permit the fluorometric detection of acidic and neutral glycosphingolipids both in test tube and on thin-layer chromatographic plates. Glycosphingolipids can
A new chiral oxathiane: synthesis, resolution and absolute configuration determination by vibrational circular dichroism.
Solladie-Cavallo A, et al.
Tetrahedron Asymmetry, 12(18), 2605-2611 (2001)
M Tanaka et al.
Journal of chromatography. B, Biomedical applications, 676(1), 87-94 (1996-02-09)
A simple and selective HPLC method for the determination of 4-hydroxymephenytoin (4-OH-M) in human urine, using a controlled potential coulometric detector equipped with a dual working electrode cell of fully porous graphite, has been developed. After acid hydrolysis of urine

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