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Details

Stereochemistry ACHIRAL
Molecular Formula C4H6O
Molecular Weight 70.0898
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-BUTYNOL

SMILES

OCCC#C

InChI

InChIKey=OTJZCIYGRUNXTP-UHFFFAOYSA-N
InChI=1S/C4H6O/c1-2-3-4-5/h1,5H,3-4H2

HIDE SMILES / InChI

Molecular Formula C4H6O
Molecular Weight 70.0898
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Total synthesis of (+/-)-kainic Acid with an aza-[2,3]-Wittig sigmatropic rearrangement as the key stereochemical determining step.
2003 Aug 8
Synthesis and structure-activity relationships of 4-alkynyloxy phenyl sulfanyl, sulfinyl, and sulfonyl alkyl hydroxamates as tumor necrosis factor-alpha converting enzyme and matrix metalloproteinase inhibitors.
2004 Dec 2
Synthesis, characterisation and molecular structure of Re(III) 2-oxacyclocarbenes stabilised by a benzoyldiazenido ligand.
2004 Mar 7
The fixation of bis(2-pyridylimino)isoindolato (BPI) ligands to dendritic carbosilanes.
2005 Apr 21
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
The use of silicon-based tethers for the Pauson-Khand reaction.
2007 Jul 6
The synthesis and enzymic hydrolysis of (E)-2-[2,3-2H2]propenyl glucosinolate: confirmation of the rearrangement of the thiohydroximate moiety.
2007 May
Synthesis of arylallenes by palladium-catalyzed retro-propargylation of homopropargyl alcohols.
2008 Apr 16
Zinc-catalyzed synthesis of pyrazolines and pyrazoles via hydrohydrazination.
2008 Jun 19
Intermolecular methoxycarbonylation of terminal alkynes catalyzed by palladium(II) bis(oxazoline) complexes.
2009
A novel enediynyl peptide inhibitor of furin that blocks processing of proPDGF-A, B and proVEGF-C.
2009 Nov 26
Catalytic enantioselective Cr-mediated propargylation: application to halichondrin synthesis.
2009 Oct 15
An efficient synthesis of (+/-)-trichostatic Acid and analogues: a new route to (+/-)-trichostatin A.
2010 Feb 19
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:50:57 GMT 2023
Edited
by admin
on Sat Dec 16 10:50:57 GMT 2023
Record UNII
P74L430293
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-BUTYNOL
Systematic Name English
3-BUTYNYL ALCOHOL
Systematic Name English
NSC-9708
Code English
4-HYDROXY-1-BUTYNE
Systematic Name English
3-BUTYN-1-OL
Systematic Name English
1-HYDROXY-3-BUTYNE
Systematic Name English
1-BUTYN-4-OL
Systematic Name English
(2-HYDROXYETHYL)ACETYLENE
Systematic Name English
Code System Code Type Description
NSC
9708
Created by admin on Sat Dec 16 10:50:57 GMT 2023 , Edited by admin on Sat Dec 16 10:50:57 GMT 2023
PRIMARY
PUBCHEM
13566
Created by admin on Sat Dec 16 10:50:57 GMT 2023 , Edited by admin on Sat Dec 16 10:50:57 GMT 2023
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CAS
927-74-2
Created by admin on Sat Dec 16 10:50:57 GMT 2023 , Edited by admin on Sat Dec 16 10:50:57 GMT 2023
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FDA UNII
P74L430293
Created by admin on Sat Dec 16 10:50:57 GMT 2023 , Edited by admin on Sat Dec 16 10:50:57 GMT 2023
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EPA CompTox
DTXSID1022136
Created by admin on Sat Dec 16 10:50:57 GMT 2023 , Edited by admin on Sat Dec 16 10:50:57 GMT 2023
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ECHA (EC/EINECS)
213-161-9
Created by admin on Sat Dec 16 10:50:57 GMT 2023 , Edited by admin on Sat Dec 16 10:50:57 GMT 2023
PRIMARY
CHEBI
27444
Created by admin on Sat Dec 16 10:50:57 GMT 2023 , Edited by admin on Sat Dec 16 10:50:57 GMT 2023
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