140856
3-Phenyl-1-propanol
98%
Synonym(s):
3-Phenylpropyl alcohol, Hydrocinnamyl alcohol
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About This Item
Linear Formula:
C6H5(CH2)3OH
CAS Number:
Molecular Weight:
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
Quality Level
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
SMILES string
OCCCc1ccccc1
InChI
1S/C9H12O/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6,10H,4,7-8H2
InChI key
VAJVDSVGBWFCLW-UHFFFAOYSA-N
General description
3-Phenyl-1-propanol is a fragrance ingredient.
Application
3-Phenyl-1-propanol was used to study the hydrogenation of trans-cinnamaldehyde using water-soluble organometallic complexes. It was used as starting reagent during the enantioselective synthesis of (S)- and (R)-dapoxetine.
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
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
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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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 140856-250G | 04061838733764 |
| 140856-50G | 04061838733771 |