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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
Study on the biosynthesis of dolichol in yeast: recognition of the prenyl chain length in polyprenol reduction.
2001 Feb
High-resolution analysis of polyprenols by supercritical fluid chromatography.
2001 Mar 9
Constituents of Pilocarpus trachylophus.
2001 Nov
[Synthesis of dolicyl- and polyprenyl sulfates].
2001 Nov-Dec
[Mechanisms of action of aerosol preparations based on Abies siberica polyprenols in experimental influenza infection].
2001 Nov-Dec
[Prophylactic efficacy of aerosol preparations based on Abies siberica polyprenols in experimental influenza infection].
2001 Nov-Dec
Rational design of enantioselective enzymes requires considerations of entropy.
2001 Sep
Chemical analysis of Ginkgo biloba leaves and extracts.
2002 Aug 16
Biosynthesis of a substituted cellulose from a mutant strain of Xanthomonas campestris.
2002 Feb 18
A general stereocontrolled, convergent synthesis of oligoprenols that parallels the biosynthetic pathway.
2002 Mar 20
Protein farnesyltransferase and protein prenylation in Plasmodium falciparum.
2002 Nov 1
Volatile compounds in Hispánico cheese manufactured using a mesophilic starter, a thermophilic starter, and bacteriocin-producing Lactococcus lactis subsp. lactis INIA 415.
2002 Nov 6
Chemical and sensorial aroma characterization of freshly distilled Calvados. 2. Identification of volatile compounds and key odorants.
2003 Jan 15
Chemical composition of the essential oils of two Rhodiola species from Tibet.
2003 Mar-Apr
The in vitro substrate regiospecificity of recombinant UGT85B1, the cyanohydrin glucosyltransferase from Sorghum bicolor.
2003 Sep
Defects in the N-linked oligosaccharide biosynthetic pathway in a Trypanosoma brucei glycosylation mutant.
2004 Apr
Heteromeric geranyl diphosphate synthase from mint: construction of a functional fusion protein and inhibition by bisphosphonate substrate analogs.
2004 Feb 1
Kinetics of the epoxidation of geraniol and model systems by dimethyldioxirane.
2004 Feb 28
[Studies on purification of polyprenol from Ginkgo biloba L. leaves].
2004 May
Sulfone and phosphinic acid analogs of decaprenolphosphoarabinose as potential anti-tuberculosis agents.
2004 Nov 1
Analysis of the volatile aroma constituents of parental and hybrid clones of pepino (Solanum muricatum).
2004 Sep 8
The occurrence of polyprenols in seeds and leaves of woody plants.
2005
Stereoselective 4-benzyloxybut-2-enylation of aldehydes via an allyl-transfer reaction using a chiral allyl donor.
2005 Jul 7
A comprehensive classification system for lipids.
2005 May
Separation of polyprenol and dolichol by monolithic silica capillary column chromatography.
2005 Oct
Studies towards the synthesis of epothilone A via organoboranes.
2005 Oct 21
Chemistry and biological activity of natural and synthetic prenyloxycoumarins.
2006
Activity of Pichia pastoris alternative cis-prenyltransferase is correlated with proliferation of peroxisomes.
2006 Feb
Precise bacterial polyprenol length control fails in Saccharomyces cerevisiae.
2007 Jun 5
Tumor-specificity and type of cell death induced by vitamin K2 derivatives and prenylalcohols.
2008 Jan-Feb
A strategy for position-selective epoxidation of polyprenols.
2008 Jun 25
Various oils and detergents enhance the microbial production of farnesol and related prenyl alcohols.
2008 Sep
Solid-phase organic synthesis of polyisoprenoid alcohols with traceless sulfone linker.
2008 Sep 19
Separation of hydrophobic metabolites using monolithic silica column in high-performance liquid chromatography and supercritical fluid chromatography.
2009 Aug
A minimalist substrate for enzymatic peptide and protein conjugation.
2009 Dec 14
Prenyl alcohol production by expression of exogenous isopentenyl diphosphate isomerase and farnesyl diphosphate synthase genes in Escherichia coli.
2009 Jan
Alkaline pH enhances farnesol production by Saccharomyces cerevisiae.
2009 Jul
Metabolomics reveals alterations in both primary and secondary metabolites by wine bacteria.
2009 Nov 25
Comparison of volatile profiles of nine litchi (Litchi chinensis Sonn.) cultivars from Southern China.
2009 Oct 28
Synthetic biology guides biofuel production.
2010
Fragrance material review on 3-methyl-2-buten-1-ol.
2010 Jan
Identification of a novel abscisic acid-regulated farnesol dehydrogenase from Arabidopsis.
2010 Nov
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:51:21 UTC 2023
Edited
by admin
on Fri Dec 15 18:51:21 UTC 2023
Record UNII
55MY0HM445
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-METHYLBUT-2-EN-1-OL
FHFI  
Systematic Name English
3-METHYL-2-BUTENOL
Systematic Name English
2-METHYL-2-BUTEN-4-OL
Systematic Name English
FEMA NO. 3647
Code English
NSC-158709
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 Fri Dec 15 18:51:21 UTC 2023 , Edited by admin on Fri Dec 15 18:51:21 UTC 2023
Code System Code Type Description
EVMPD
SUB130463
Created by admin on Fri Dec 15 18:51:21 UTC 2023 , Edited by admin on Fri Dec 15 18:51:21 UTC 2023
PRIMARY
SMS_ID
100000156480
Created by admin on Fri Dec 15 18:51:21 UTC 2023 , Edited by admin on Fri Dec 15 18:51:21 UTC 2023
PRIMARY
EPA CompTox
DTXSID2027206
Created by admin on Fri Dec 15 18:51:21 UTC 2023 , Edited by admin on Fri Dec 15 18:51:21 UTC 2023
PRIMARY
CAS
556-82-1
Created by admin on Fri Dec 15 18:51:21 UTC 2023 , Edited by admin on Fri Dec 15 18:51:21 UTC 2023
PRIMARY
PUBCHEM
11173
Created by admin on Fri Dec 15 18:51:21 UTC 2023 , Edited by admin on Fri Dec 15 18:51:21 UTC 2023
PRIMARY
JECFA MONOGRAPH
1209
Created by admin on Fri Dec 15 18:51:21 UTC 2023 , Edited by admin on Fri Dec 15 18:51:21 UTC 2023
PRIMARY
MESH
C009034
Created by admin on Fri Dec 15 18:51:21 UTC 2023 , Edited by admin on Fri Dec 15 18:51:21 UTC 2023
PRIMARY
CHEBI
16019
Created by admin on Fri Dec 15 18:51:21 UTC 2023 , Edited by admin on Fri Dec 15 18:51:21 UTC 2023
PRIMARY
FDA UNII
55MY0HM445
Created by admin on Fri Dec 15 18:51:21 UTC 2023 , Edited by admin on Fri Dec 15 18:51:21 UTC 2023
PRIMARY
ECHA (EC/EINECS)
209-141-4
Created by admin on Fri Dec 15 18:51:21 UTC 2023 , Edited by admin on Fri Dec 15 18:51:21 UTC 2023
PRIMARY
NSC
158709
Created by admin on Fri Dec 15 18:51:21 UTC 2023 , Edited by admin on Fri Dec 15 18:51:21 UTC 2023
PRIMARY
WIKIPEDIA
PRENOL
Created by admin on Fri Dec 15 18:51:21 UTC 2023 , Edited by admin on Fri Dec 15 18:51:21 UTC 2023
PRIMARY