459798
Allyl alcohol
≥98.5%
Synonym(s):
2-Propen-1-ol
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About This Item
Linear Formula:
CH2=CHCH2OH
CAS Number:
Molecular Weight:
58.08
UNSPSC Code:
12352200
NACRES:
NA.21
PubChem Substance ID:
EC Number:
203-470-7
Beilstein/REAXYS Number:
605307
MDL number:
Assay:
≥98.5%
vapor density
2 (vs air)
Quality Level
vapor pressure
23.8 mmHg ( 25 °C)
assay
≥98.5%
autoignition temp.
712 °F
expl. lim.
18 %
refractive index
n20/D 1.412 (lit.)
bp
96-98 °C (lit.)
mp
−129 °C (lit.)
density
0.854 g/mL at 25 °C (lit.)
functional group
hydroxyl
SMILES string
OCC=C
InChI
1S/C3H6O/c1-2-3-4/h2,4H,1,3H2
InChI key
XXROGKLTLUQVRX-UHFFFAOYSA-N
Application
Used to induce a mouse model of liver damage that has been used to study the mechanisms of hepatotoxicity and hepatic stem cell-mediated repair.
Packaging
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signalword
Danger
Hazard Classifications
Acute Tox. 2 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 2 - Repr. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
71.6 °F - closed cup
flash_point_c
22 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Madeleine C Warner et al.
Organic letters, 14(19), 5094-5097 (2012-09-26)
A general and efficient route for the synthesis of enantiomerically pure α-substituted ketones and the corresponding lactones has been developed. Ruthenium- and enzyme-catalyzed dynamic kinetic resolution (DKR) with a subsequent Cu-catalyzed α-allylic substitution are the key steps of the route.
Copper-catalyzed tandem trifluoromethylation/semipinacol rearrangement of allylic alcohols.
Zhi-Min Chen et al.
Angewandte Chemie (International ed. in English), 52(37), 9781-9785 (2013-07-23)
J Stephen Clark et al.
The Journal of organic chemistry, 78(2), 673-696 (2012-12-12)
The enantioselective total syntheses of 10 cladiellin natural products have been completed, starting from the known allylic alcohol (+)-14, which can be prepared in large quantities. The bridged tricyclic core of the cladiellins has been constructed via three ring-forming reactions: