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Details

Stereochemistry ACHIRAL
Molecular Formula C4H8O
Molecular Weight 72.1057
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-BUTEN-1-OL

SMILES

OCCC=C

InChI

InChIKey=ZSPTYLOMNJNZNG-UHFFFAOYSA-N
InChI=1S/C4H8O/c1-2-3-4-5/h2,5H,1,3-4H2

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Diastereoselective synthesis of polysubstituted tetrahydropyrans and thiacyclohexanes via indium trichloride mediated cyclizations.
2001 Feb 9
Enantioselective total synthesis of eunicenone A.
2001 Mar 7
Methylation methods for the quantitative analysis of conjugated linoleic acid (CLA) isomers in various lipid samples.
2002 Feb 27
Application of tin and nanometer tin in allylation of carbonyl compounds in tap water.
2002 May 16
Synthesis of (+/-)-secosyrin 1 and a formal synthesis of (-)-secosyrin 1.
2004 Feb 19
Calorimetric and computational study of 3-buten-1-ol and 3-butyn-1-ol. Estimation of the enthalpies of formation of 1-alkenols and 1-alkynols.
2005 Sep 1
Rapid stereocontrolled assembly of the fully substituted C-aryl glycoside of kendomycin with a Prins cyclization: a formal synthesis.
2006 Jun 14
Synthesis of 1,2,4-trioxepanes and 1,2,4-trioxocanes via photooxygenation of homoallylic alcohols.
2006 Nov 24
Highly enantioselective carbonyl-ene reactions catalyzed by a hindered silyl-salen-cobalt complex.
2007 Sep 27
Rhodium-catalyzed allylation of aldehydes with homoallylic alcohols by retroallylation and isomerization to saturated ketones with conventional or microwave heating.
2008 Jan 4
Catalytic enantioselective allyl- and crotylboration of aldehydes using chiral diol x SnCl4 complexes. optimization, substrate scope and mechanistic investigations.
2008 Jul 2
Oxygen-directed intramolecular hydroboration.
2008 Jul 23
Asymmetric allylation of methyl ketones by using chiral phenyl carbinols.
2009 Jun 15
Patents
Name Type Language
3-BUTEN-1-OL
Systematic Name English
NSC-60194
Code English
3-BUTENE-1-OL
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID2060836
Created by admin on Fri Dec 15 18:05:17 GMT 2023 , Edited by admin on Fri Dec 15 18:05:17 GMT 2023
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FDA UNII
3DB2KRM1I9
Created by admin on Fri Dec 15 18:05:17 GMT 2023 , Edited by admin on Fri Dec 15 18:05:17 GMT 2023
PRIMARY
CAS
627-27-0
Created by admin on Fri Dec 15 18:05:17 GMT 2023 , Edited by admin on Fri Dec 15 18:05:17 GMT 2023
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NSC
60194
Created by admin on Fri Dec 15 18:05:17 GMT 2023 , Edited by admin on Fri Dec 15 18:05:17 GMT 2023
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PUBCHEM
69389
Created by admin on Fri Dec 15 18:05:17 GMT 2023 , Edited by admin on Fri Dec 15 18:05:17 GMT 2023
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ECHA (EC/EINECS)
210-991-3
Created by admin on Fri Dec 15 18:05:17 GMT 2023 , Edited by admin on Fri Dec 15 18:05:17 GMT 2023
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