Weight | 86.134 g/mol |
---|---|
Formula | C5H10O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
1-PENTEN-3-OL (616-25-1)
1-pentene-3-ol
Score:
#68 in Physical chemistry
,
#1837 in Physics
,
#5727 in Chemistry
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- Sigma-Aldrich - 1-PENTEN-3-OL28.50 - 699.00 USD
- Fisher Scientific - Search for 1-PENTEN-3-OL
- TCI - 1-PENTEN-3-OL25.00 - 93.00 USD
- Studies of Sites of Action of a New Plant Growth Retardant (E)-1-(4-Chlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-1-penten-3-ol (S-3307) and Comparative Effects of Its Stereoisomers in a Cell-Free System from Cucurbita maxima (Plant and Cell Physiology, 1985)
- Effects of a New Plant Growth Retardant (E)-1-(4-Chlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-1-penten-3-ol (S-3307) on the Growth and Gibberellin Content of Rice Plants (Plant and Cell Physiology, 1984)
- Rate Coefficients and Product Yields from Reaction of OH with 1-Penten-3-ol, (Z)-2-Penten-1-ol, and Allyl Alcohol (2-Propen-1-ol) (Journal of Physical Chemistry A, 2001)
- Palladium(II)-catalyzed exchange and isomerization reactions. 14. Kinetics and stereochemistry of the isomerization and water exchange of 2-(methyl-d3)-4-methyl-1,1,1,5,5,5-hexafluoro-3-penten-2-ol in aqueous solution catalyzed by PdCl42-. Two new mechanistic probes for catalytic chemistry (Organometallics, 1991)
- Photooxidation of Leaf-Wound Oxygenated Compounds, 1-Penten-3-ol, (Z)-3-Hexen-1-ol, and 1-Penten-3-one, Initiated by OH Radicals and Sunlight (Environmental Science & Technology, 2009)
- Palladium(II)-catalyzed exchange and isomerization reactions. 15 : Kinetics and stereochemistry of the isomerization of 2-(methyl-d3)-4-methyl-1,1,1,5,5,5-hexafluoro-3-penten-2-ol in aqueous solution catalyzed by PdCI42- at high chloride concentrations (Organometallics, 1992)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1-pentene-3-ol
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SMILESCCC(C=C)O
-
InChIKeyVHVMXWZXFBOANQ-UHFFFAOYSA-N
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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