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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
Quantification of 4'-geranyloxyferulic acid, a new natural colon cancer chemopreventive agent, by HPLC-DAD in grapefruit skin extract.
2010-10-10
The Alveolate Perkinsus marinus: biological insights from EST gene discovery.
2010-04-07
Various Terpenoids Derived from Herbal and Dietary Plants Function as PPAR Modulators and Regulate Carbohydrate and Lipid Metabolism.
2010
Comparison of volatile profiles of nine litchi (Litchi chinensis Sonn.) cultivars from Southern China.
2009-10-28
G-protein coupled receptor signaling architecture of mammalian immune cells.
2009
Rate coefficients for the reaction of OH with a series of unsaturated alcohols between 263 and 371 K.
2008-05-15
Chemistry and pharmacology of oxyprenylated secondary plant metabolites.
2007-04
Electrophysiological and behavioral responses of Ips subelongatus to semiochemicals from its hosts, non-hosts, and conspecifics in China.
2007-02
Production of volatile compounds by Rhizopus oligosporus during soybean and barley tempeh fermentation.
2007-01-25
In vitro inhibitory activity of boropinic acid against Helicobacter pylori.
2006-11-01
Rooting the tree of life by transition analyses.
2006-07-11
Comprehensive two-dimensional normal-phase (adsorption)-reversed-phase liquid chromatography.
2004-05-01
The in vitro substrate regiospecificity of recombinant UGT85B1, the cyanohydrin glucosyltransferase from Sorghum bicolor.
2003-09
Volatile metabolites from actinomycetes.
2002-04-24
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.
2002-02
Volatile flavor constituents of acerola (Malpighia emarginata DC.) fruit.
2001-12
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.
2001-11-30
Synthesis of unsaturated carboacyclic nucleoside analogues via Mitsunobu reactions.
2000-07-14
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:17:35 GMT 2025
Edited
by admin
on Mon Mar 31 19:17:35 GMT 2025
Record UNII
KJ25C8CPFA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-METHYL-3-BUTEN-1-OL
Systematic Name English
NSC-122673
Preferred 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
3-METHYLBUT-3-EN-1-OL
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
212-110-8
Created by admin on Mon Mar 31 19:17:35 GMT 2025 , Edited by admin on Mon Mar 31 19:17:35 GMT 2025
PRIMARY
SMS_ID
300000053106
Created by admin on Mon Mar 31 19:17:35 GMT 2025 , Edited by admin on Mon Mar 31 19:17:35 GMT 2025
PRIMARY
NSC
122673
Created by admin on Mon Mar 31 19:17:35 GMT 2025 , Edited by admin on Mon Mar 31 19:17:35 GMT 2025
PRIMARY
CAS
763-32-6
Created by admin on Mon Mar 31 19:17:35 GMT 2025 , Edited by admin on Mon Mar 31 19:17:35 GMT 2025
PRIMARY
FDA UNII
KJ25C8CPFA
Created by admin on Mon Mar 31 19:17:35 GMT 2025 , Edited by admin on Mon Mar 31 19:17:35 GMT 2025
PRIMARY
WIKIPEDIA
ISOPRENOL
Created by admin on Mon Mar 31 19:17:35 GMT 2025 , Edited by admin on Mon Mar 31 19:17:35 GMT 2025
PRIMARY
CHEBI
62898
Created by admin on Mon Mar 31 19:17:35 GMT 2025 , Edited by admin on Mon Mar 31 19:17:35 GMT 2025
PRIMARY
EPA CompTox
DTXSID4052506
Created by admin on Mon Mar 31 19:17:35 GMT 2025 , Edited by admin on Mon Mar 31 19:17:35 GMT 2025
PRIMARY
PUBCHEM
12988
Created by admin on Mon Mar 31 19:17:35 GMT 2025 , Edited by admin on Mon Mar 31 19:17:35 GMT 2025
PRIMARY