Details
Stereochemistry | ACHIRAL |
Molecular Formula | C5H10O |
Molecular Weight | 86.1323 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=C)CCO
InChI
InChIKey=CPJRRXSHAYUTGL-UHFFFAOYSA-N
InChI=1S/C5H10O/c1-5(2)3-4-6/h6H,1,3-4H2,2H3
Approval Year
PubMed
Title | Date | PubMed |
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Synthesis of unsaturated carboacyclic nucleoside analogues via Mitsunobu reactions. | 2000 May-Jun |
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Studies on the alkylation of 3-methyl-3-buten-1-ol dianion: an efficient synthesis of 3-methylene-1-alkanols including a San Jose scale sex pheromone. | 2001 Nov 30 |
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Volatile metabolites from actinomycetes. | 2002 Apr 24 |
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The in vitro substrate regiospecificity of recombinant UGT85B1, the cyanohydrin glucosyltransferase from Sorghum bicolor. | 2003 Sep |
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Rooting the tree of life by transition analyses. | 2006 Jul 11 |
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In vitro inhibitory activity of boropinic acid against Helicobacter pylori. | 2006 Nov 1 |
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Chemistry and pharmacology of oxyprenylated secondary plant metabolites. | 2007 Apr |
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Production of volatile compounds by Rhizopus oligosporus during soybean and barley tempeh fermentation. | 2007 Jan 25 |
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Comparison of volatile profiles of nine litchi (Litchi chinensis Sonn.) cultivars from Southern China. | 2009 Oct 28 |
Patents
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212-110-8
Created by
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122673
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763-32-6
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KJ25C8CPFA
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ISOPRENOL
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62898
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DTXSID4052506
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12988
Created by
admin on Fri Dec 15 18:38:15 GMT 2023 , Edited by admin on Fri Dec 15 18:38:15 GMT 2023
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SUBSTANCE RECORD