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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-METHYLBUT-2-EN-1-OL

SMILES

CC(C)=CCO

InChI

InChIKey=ASUAYTHWZCLXAN-UHFFFAOYSA-N
InChI=1S/C5H10O/c1-5(2)3-4-6/h3,6H,4H2,1-2H3

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
Identification of a novel abscisic acid-regulated farnesol dehydrogenase from Arabidopsis.
2010-11
Fragrance material review on 3-methyl-2-buten-1-ol.
2010-01
Synthetic biology guides biofuel production.
2010
A minimalist substrate for enzymatic peptide and protein conjugation.
2009-12-14
Metabolomics reveals alterations in both primary and secondary metabolites by wine bacteria.
2009-11-25
Comparison of volatile profiles of nine litchi (Litchi chinensis Sonn.) cultivars from Southern China.
2009-10-28
Separation of hydrophobic metabolites using monolithic silica column in high-performance liquid chromatography and supercritical fluid chromatography.
2009-08
Alkaline pH enhances farnesol production by Saccharomyces cerevisiae.
2009-07
Prenyl alcohol production by expression of exogenous isopentenyl diphosphate isomerase and farnesyl diphosphate synthase genes in Escherichia coli.
2009-01
Solid-phase organic synthesis of polyisoprenoid alcohols with traceless sulfone linker.
2008-09-19
Various oils and detergents enhance the microbial production of farnesol and related prenyl alcohols.
2008-09
A strategy for position-selective epoxidation of polyprenols.
2008-06-25
Tumor-specificity and type of cell death induced by vitamin K2 derivatives and prenylalcohols.
2008-04-04
Antidyslipidemic activity of polyprenol from Coccinia grandis in high-fat diet-fed hamster model.
2007-12
Precise bacterial polyprenol length control fails in Saccharomyces cerevisiae.
2007-06-05
Alloprenols: novel alpha-trans-polyprenols of Allophylus caudatus.
2007-06
Chemistry and pharmacology of oxyprenylated secondary plant metabolites.
2007-04
Synthesis of O-prenylated and O-geranylated derivatives of 5-benzylidene2,4-thiazolidinediones and evaluation of their free radical scavenging activity as well as effect on some phase II antioxidant/detoxifying enzymes.
2007-03-01
The search for polyprenols in dendroflora of Vietnam.
2007
Analysis of ubiquinones, dolichols, and dolichol diphosphate-oligosaccharides by liquid chromatography-electrospray ionization-mass spectrometry.
2007
Comparative analysis of volatile constituents from mice and their urine.
2006-06
A new approach for the asymmetric total synthesis of umbelactone.
2006-05-05
Activity of Pichia pastoris alternative cis-prenyltransferase is correlated with proliferation of peroxisomes.
2006-02
Chemistry and biological activity of natural and synthetic prenyloxycoumarins.
2006
Studies towards the synthesis of epothilone A via organoboranes.
2005-10-21
Separation of polyprenol and dolichol by monolithic silica capillary column chromatography.
2005-10
Stereoselective 4-benzyloxybut-2-enylation of aldehydes via an allyl-transfer reaction using a chiral allyl donor.
2005-07-07
Polyprenyl lipid synthesis in mammalian cells expressing human cis-prenyl transferase.
2005-06-03
A comprehensive classification system for lipids.
2005-05
The occurrence of polyprenols in seeds and leaves of woody plants.
2005
Light conditions alter accumulation of long chain polyprenols in leaves of trees and shrubs throughout the vegetation season.
2005
Sulfone and phosphinic acid analogs of decaprenolphosphoarabinose as potential anti-tuberculosis agents.
2004-11-01
Analysis of the volatile aroma constituents of parental and hybrid clones of pepino (Solanum muricatum).
2004-09-08
[Studies on purification of polyprenol from Ginkgo biloba L. leaves].
2004-05
Defects in the N-linked oligosaccharide biosynthetic pathway in a Trypanosoma brucei glycosylation mutant.
2004-04
Kinetics of the epoxidation of geraniol and model systems by dimethyldioxirane.
2004-02-28
Heteromeric geranyl diphosphate synthase from mint: construction of a functional fusion protein and inhibition by bisphosphonate substrate analogs.
2004-02-01
The in vitro substrate regiospecificity of recombinant UGT85B1, the cyanohydrin glucosyltransferase from Sorghum bicolor.
2003-09
Chemical composition of the essential oils of two Rhodiola species from Tibet.
2003-04-25
Chemical and sensorial aroma characterization of freshly distilled Calvados. 2. Identification of volatile compounds and key odorants.
2003-01-15
Volatile compounds in Hispánico cheese manufactured using a mesophilic starter, a thermophilic starter, and bacteriocin-producing Lactococcus lactis subsp. lactis INIA 415.
2002-11-06
Protein farnesyltransferase and protein prenylation in Plasmodium falciparum.
2002-11-01
Chemical analysis of Ginkgo biloba leaves and extracts.
2002-08-16
A general stereocontrolled, convergent synthesis of oligoprenols that parallels the biosynthetic pathway.
2002-03-20
Biosynthesis of a substituted cellulose from a mutant strain of Xanthomonas campestris.
2002-02-18
[Synthesis of dolicyl- and polyprenyl sulfates].
2002-01-29
[Mechanisms of action of aerosol preparations based on Abies siberica polyprenols in experimental influenza infection].
2002-01-12
[Prophylactic efficacy of aerosol preparations based on Abies siberica polyprenols in experimental influenza infection].
2002-01-12
Constituents of Pilocarpus trachylophus.
2001-11
Rational design of enantioselective enzymes requires considerations of entropy.
2001-09
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:22:45 GMT 2025
Edited
by admin
on Mon Mar 31 19:22:45 GMT 2025
Record UNII
55MY0HM445
Record Status Validated (UNII)
Record Version
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Name Type Language
3-METHYLBUT-2-EN-1-OL
FHFI  
Systematic Name English
NSC-158709
Preferred Name English
3-METHYL-2-BUTENOL
Systematic Name English
2-METHYL-2-BUTEN-4-OL
Systematic Name English
FEMA NO. 3647
Code English
ISOPENT-2-EN-1-OL
Common Name English
PRENYL ALCOHOL
Systematic Name English
3,3-DIMETHYLALLYL ALCOHOL
Systematic Name English
3-METHYL-2-BUTEN-1-OL
Systematic Name English
PRENOL
Common Name English
2-BUTEN-1-OL, 3-METHYL-
Systematic Name English
3-METHYLBUT-2-EN-1-OL [FHFI]
Common Name English
DIMETHYLALLYL ALCOHOL
Systematic Name English
.GAMMA.,.GAMMA.-DIMETHYLALLYL ALCOHOL
Common Name English
3-METHYL-2-BUTENE-1-OL
Systematic Name English
3-METHYL-2-BUTENYL ALCOHOL
Systematic Name English
3-METHYLCROTYL ALCOHOL
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION 3-METHYL-2-BUTEN-1-OL
Created by admin on Mon Mar 31 19:22:45 GMT 2025 , Edited by admin on Mon Mar 31 19:22:45 GMT 2025
Code System Code Type Description
EVMPD
SUB130463
Created by admin on Mon Mar 31 19:22:45 GMT 2025 , Edited by admin on Mon Mar 31 19:22:45 GMT 2025
PRIMARY
SMS_ID
100000156480
Created by admin on Mon Mar 31 19:22:45 GMT 2025 , Edited by admin on Mon Mar 31 19:22:45 GMT 2025
PRIMARY
EPA CompTox
DTXSID2027206
Created by admin on Mon Mar 31 19:22:45 GMT 2025 , Edited by admin on Mon Mar 31 19:22:45 GMT 2025
PRIMARY
CAS
556-82-1
Created by admin on Mon Mar 31 19:22:45 GMT 2025 , Edited by admin on Mon Mar 31 19:22:45 GMT 2025
PRIMARY
PUBCHEM
11173
Created by admin on Mon Mar 31 19:22:45 GMT 2025 , Edited by admin on Mon Mar 31 19:22:45 GMT 2025
PRIMARY
JECFA MONOGRAPH
1209
Created by admin on Mon Mar 31 19:22:45 GMT 2025 , Edited by admin on Mon Mar 31 19:22:45 GMT 2025
PRIMARY
MESH
C009034
Created by admin on Mon Mar 31 19:22:45 GMT 2025 , Edited by admin on Mon Mar 31 19:22:45 GMT 2025
PRIMARY
CHEBI
16019
Created by admin on Mon Mar 31 19:22:45 GMT 2025 , Edited by admin on Mon Mar 31 19:22:45 GMT 2025
PRIMARY
FDA UNII
55MY0HM445
Created by admin on Mon Mar 31 19:22:45 GMT 2025 , Edited by admin on Mon Mar 31 19:22:45 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-141-4
Created by admin on Mon Mar 31 19:22:45 GMT 2025 , Edited by admin on Mon Mar 31 19:22:45 GMT 2025
PRIMARY
NSC
158709
Created by admin on Mon Mar 31 19:22:45 GMT 2025 , Edited by admin on Mon Mar 31 19:22:45 GMT 2025
PRIMARY
WIKIPEDIA
PRENOL
Created by admin on Mon Mar 31 19:22:45 GMT 2025 , Edited by admin on Mon Mar 31 19:22:45 GMT 2025
PRIMARY