140856
3-苯基-1-丙醇
98%
别名:
3-苯丙醇, 氢化肉桂醇
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线性分子式:
C6H5(CH2)3OH
化学文摘社编号:
分子量:
136.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-587-6
Beilstein/REAXYS Number:
1857542
MDL number:
Assay:
98%
Form:
liquid
InChI key
VAJVDSVGBWFCLW-UHFFFAOYSA-N
InChI
1S/C9H12O/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6,10H,4,7-8H2
SMILES string
OCCCc1ccccc1
assay
98%
form
liquid
refractive index
n20/D 1.526 (lit.)
bp
119-121 °C/12 mmHg (lit.)
mp
−18 °C (lit.)
density
1.001 g/mL at 20 °C (lit.)
functional group
hydroxyl, phenyl
Quality Level
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General description
3-苯基-1-丙醇是一种香味成分 。
Application
3-苯基-1-丙醇被用于使用水溶性有机金属配合物研究 反式 -肉桂醛的氢化反应。在 (S)-和 (R)-达泊西汀的对映选择性合成中用作起始试剂 。
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
248.0 °F - closed cup
flash_point_c
120 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
The regioselective biphasic hydrogenation of trans-cinnaldehyde by meta sulfonatophenyl-diphenylphosphine (TPPMS) Ru (II) and Os (II) species. The influence of ionic strength, ligand tensoactivity and metal nature in the selective production of the unsaturated alcohol.
Lopez-Linares F, et al.
J. Mol. Catal. A: Chem., 145(1), 61-68 (1999)
S P Bhatia et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 49 Suppl 2, S246-S251 (2011-08-23)
A toxicologic and dermatologic review of 3-phenyl-1-propanol when used as a fragrance ingredient is presented. 3-Phenyl-1-propanol is a member of the fragrance structural group cinnamyl phenylpropyl compounds. The common characteristic structural element of cinnamyl phenylpropyl materials is an aryl substituted
Jörgen Samuelsson et al.
Journal of chromatography. A, 1217(46), 7215-7221 (2010-10-12)
The elution by characteristic points (ECP) method is a very rapid and precise method for determination of the phase system equilibrium of phase systems in broad solute concentration ranges. Thus, the method is especially suitable for rapid characterization of high
Soyeong Kang et al.
The Journal of organic chemistry, 75(1), 237-240 (2009-12-05)
A highly efficient, enantioselective sequence has been developed for the synthesis of (S)- and (R)-dapoxetine. The pathways involve the intermediacy of the 6-membered-ring sulfamate esters 4, which were generated by Du Bois asymmetric C-H amination reactions of the prochiral sulfamate
Ryan L Jones et al.
Langmuir : the ACS journal of surfaces and colloids, 26(21), 16355-16361 (2010-09-23)
Self-assembled monolayers (SAMs) have been widely studied as potential lubricants for microelectromechanical system (MEMS) devices. However, these single-layer films have nominally been found to be insufficient for mitigating wear in sliding contacts because of their rapid breakdown under the high
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