461407
(R)-(+)-2-苯基-1-丙醇
98%
别名:
(R)-β-甲基苯乙醇, (R)-2-苯丙醇
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关于此项目
线性分子式:
CH3CH(C6H5)CH2OH
化学文摘社编号:
分子量:
136.19
UNSPSC Code:
12352002
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2637521
InChI
1S/C9H12O/c1-8(7-10)9-5-3-2-4-6-9/h2-6,8,10H,7H2,1H3/t8-/m0/s1
SMILES string
C[C@@H](CO)c1ccccc1
InChI key
RNDNSYIPLPAXAZ-QMMMGPOBSA-N
assay
98%
optical activity
[α]22/D +17°, neat
refractive index
n20/D 1.526 (lit.)
bp
220 °C (lit.)
density
1 g/mL at 25 °C (lit.)
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
226.4 °F - closed cup
flash_point_c
108 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
W Gielsdorf et al.
Zeitschrift fur Rechtsmedizin. Journal of legal medicine, 89(3), 191-195 (1982-01-01)
The FAB (Fast Atom Bombardment)-mass spectrometric ionization technique, which has now been available for about 1 year, has been successfully employed in forensic toxicology. The mass spectral behaviour of some representative drug-glucuronides (Codeine, p-Nitrophenol and 2-Phenyl-1-propanol) were studied by positive-
I F Gaunt et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 20(5), 519-525 (1982-10-01)
Phenylpropan-1-ol was added to the diet of groups of 15 male and 15 female rats to provide intakes of 0 (control), 10, 40 or 160 mg/kg/day for 13 wk. No effects on body weight, food intake, water intake, haematology, semi-quantitative
K R Henne et al.
Biochemistry, 40(29), 8597-8605 (2001-07-18)
The active site topography of rabbit CYP4B1 has been studied relative to CYP2B1 and CYP102 using a variety of aromatic probe substrates. Oxidation of the prochiral substrate cumene by CYP4B1, but not CYP2B1 or CYP102, resulted in the formation of
S Goenechea et al.
Zeitschrift fur Rechtsmedizin. Journal of legal medicine, 97(2), 83-88 (1986-01-01)
The behaviour of 2-phenyl-1-propanol (I) and 2-phenyl-2-propanol (II) and their glucuronides with HCl has been investigated. While I shows a high acidic constancy, II undergoes a partial conversion into 2-phenylpropane (III) which itself yields numerous products. The glucosidic bond of
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