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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
Structure of 3-METHYL-3-BUTEN-1-OL

SMILES

CC(=C)CCO

InChI

InChIKey=CPJRRXSHAYUTGL-UHFFFAOYSA-N
InChI=1S/C5H10O/c1-5(2)3-4-6/h6H,1,3-4H2,2H3

HIDE SMILES / InChI

Molecular Formula C5H10O
Molecular Weight 86.1323
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis of unsaturated carboacyclic nucleoside analogues via Mitsunobu reactions.
2000 May-Jun
Conformational preferences of anticodon 3'-adjacent hypermodified nucleic acid base cis-or trans-zeatin and its 2-methylthio derivative, cis-or trans- ms(2)zeatin.
2002 Feb
The in vitro substrate regiospecificity of recombinant UGT85B1, the cyanohydrin glucosyltransferase from Sorghum bicolor.
2003 Sep
Comprehensive two-dimensional normal-phase (adsorption)-reversed-phase liquid chromatography.
2004 May 1
Rooting the tree of life by transition analyses.
2006 Jul 11
In vitro inhibitory activity of boropinic acid against Helicobacter pylori.
2006 Nov 1
Chemistry and pharmacology of oxyprenylated secondary plant metabolites.
2007 Apr
Production of volatile compounds by Rhizopus oligosporus during soybean and barley tempeh fermentation.
2007 Jan 25
Rate coefficients for the reaction of OH with a series of unsaturated alcohols between 263 and 371 K.
2008 May 15
G-protein coupled receptor signaling architecture of mammalian immune cells.
2009
Comparison of volatile profiles of nine litchi (Litchi chinensis Sonn.) cultivars from Southern China.
2009 Oct 28
Various Terpenoids Derived from Herbal and Dietary Plants Function as PPAR Modulators and Regulate Carbohydrate and Lipid Metabolism.
2010
The Alveolate Perkinsus marinus: biological insights from EST gene discovery.
2010 Apr 7
Quantification of 4'-geranyloxyferulic acid, a new natural colon cancer chemopreventive agent, by HPLC-DAD in grapefruit skin extract.
2010 Oct 10
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:38:15 GMT 2023
Edited
by admin
on Fri Dec 15 18:38:15 GMT 2023
Record UNII
KJ25C8CPFA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-METHYL-3-BUTEN-1-OL
Systematic Name English
METHALLYLCARBINOL
Systematic Name English
2-METHYL-1-BUTEN-4-OL
Systematic Name English
3-ISOPENTENYL ALCOHOL
Common Name English
ISOPROPENYLETHYL ALCOHOL
Systematic Name English
3-METHYLENEBUTAN-1-OL
Systematic Name English
2-METHYL-4-HYDROXY-1-BUTENE
Systematic Name English
3-BUTEN-1-OL, 3-METHYL-
Systematic Name English
3-METHYL-3-BUTENOL
Systematic Name English
4-HYDROXY-2-METHYL-1-BUTENE
Systematic Name English
ISOPRENOL
Common Name English
NSC-122673
Code English
3-METHYLBUT-3-EN-1-OL
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
212-110-8
Created by admin on Fri Dec 15 18:38:15 GMT 2023 , Edited by admin on Fri Dec 15 18:38:15 GMT 2023
PRIMARY
NSC
122673
Created by admin on Fri Dec 15 18:38:15 GMT 2023 , Edited by admin on Fri Dec 15 18:38:15 GMT 2023
PRIMARY
CAS
763-32-6
Created by admin on Fri Dec 15 18:38:15 GMT 2023 , Edited by admin on Fri Dec 15 18:38:15 GMT 2023
PRIMARY
FDA UNII
KJ25C8CPFA
Created by admin on Fri Dec 15 18:38:15 GMT 2023 , Edited by admin on Fri Dec 15 18:38:15 GMT 2023
PRIMARY
WIKIPEDIA
ISOPRENOL
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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CHEBI
62898
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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EPA CompTox
DTXSID4052506
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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PUBCHEM
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
PRIMARY