219975
5-羟基-1-四氢萘酮
99%
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关于此项目
经验公式（希尔记法）:
C10H10O2
化学文摘社编号:
分子量:
162.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
248-958-0
Beilstein/REAXYS Number:
2437410
MDL number:
产品名称
5-羟基-1-四氢萘酮, 99%
InChI key
YPPZCRZRQHFRBH-UHFFFAOYSA-N
InChI
1S/C10H10O2/c11-9-5-1-3-7-8(9)4-2-6-10(7)12/h1,3,5,11H,2,4,6H2
SMILES string
Oc1cccc2C(=O)CCCc12
assay
99%
mp
206-209 °C (lit.)
functional group
ketone
Quality Level
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Application
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
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)
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
Studies on Quinones. Part 22.'Synthesis of 1-Benzazepine-6, 9-Quinone Derivatives.
Valderrama JA, et al.
Synthetic Communications, 22(4), 629-640 (1992)
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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