3-Benzyloxy-propan-1-ol
Names
[ CAS No. ]:
4799-68-2
[ Name ]:
3-Benzyloxy-propan-1-ol
[Synonym ]:
1-Propanol, 3- (benzyloxy)-
1-Propanol, 3- (phenylmethoxy)-
1-Propanol, 3-(phenylmethoxy)-
3-(Benzyloxy)-1-propanol
3-phenylmethoxypropan-1-ol
MFCD00029659
3-(Benzyloxy)propan-1-ol
3-Benzyloxy-1-Propanol
1-Propanol, 3-(benzyloxy)-
3-Benzyloxy-propan-1-ol
Chemical & Physical Properties
[ Density]:
1.0±0.1 g/cm3
[ Boiling Point ]:
274.3±0.0 °C at 760 mmHg
[ Melting Point ]:
38ºC
[ Molecular Formula ]:
C10H14O2
[ Molecular Weight ]:
166.217
[ Flash Point ]:
126.9±14.6 °C
[ Exact Mass ]:
166.099380
[ PSA ]:
29.46000
[ LogP ]:
1.67
[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C
[ Index of Refraction ]:
1.520
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
[ Hazard Codes ]:
Xi:Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S37/39
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2909499000
Synthetic Route
Customs
[ HS Code ]: 2909499000
[ Summary ]:
2909499000. ether-alcohols and their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:5.5%. General tariff:30.0%
Articles
Org. Lett. 14(12) , 2992-5, (2012)
The ruthenium catalyzed selective sp(3) C-O cleavage with amide formation was reported in reactions of 3-alkoxy-1-propanol derivatives and amines. The cleavage only occurs at the C3-O position even wi...
Total synthesis of (+)-cocaine via desymmetrization of a meso-dialdehyde.Org. Lett. 6(19) , 3305-8, (2004)
[reaction: see text] The total synthesis of (+)-cocaine is described. An extension of the recently reported proline catalyzed intramolecular enol-exo-aldol reaction to a meso-dialdehyde provided the t...
Synthesis of galactosyl phosphate diester derivatives of nucleosides.Carbohydr. Res. 257(2) , 323-30, (1994)