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Details

Stereochemistry ACHIRAL
Molecular Formula C6H10
Molecular Weight 82.1436
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-Hexyne

SMILES

CCCCC#C

InChI

InChIKey=CGHIBGNXEGJPQZ-UHFFFAOYSA-N
InChI=1S/C6H10/c1-3-5-6-4-2/h1H,4-6H2,2H3

HIDE SMILES / InChI

Molecular Formula C6H10
Molecular Weight 82.1436
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Fluorescent DNA: the development of 7-deazapurine nucleoside triphosphates applicable for sequencing at the single molecule level.
2001 Apr 13
Ruthenium complex-catalyzed anti-Markovnikov hydration of terminal alkynes.
2001 Mar 8
First highly stereoselective synthesis of fungicide systhane.
2002 Jan 10
Adducts of thianthrene- and phenoxathiin cation radical tetrafluoroborates to 1-alkynes. Structures and formation of 1-(5-thianthreniumyl)- and 1-(10-phenoxathiiniumyl)alkynes on alumina leading to alpha-ketoylides and alpha-ketols.
2005 Nov 25
Reactivity of alkynes containing alpha-hydrogen atoms with a triruthenium hydrido carbonyl cluster: alkenyl versus allyl cluster derivatives.
2005 Oct 7
Quassinoid support studies: fused carbocycle synthesis from benzoic acid derivatives via 5-hexynyl and 6-heptynyl radical cyclizations.
2006 Sep 28
Sex pheromone of Lonomia obliqua: daily rhythm of production, identification, and synthesis.
2007 Mar
Revealing phenylium, phenonium, vinylenephenonium, and benzenium ions in solution.
2008
Conversion of methane to liquid products, hydrogen, and ammonia with environmentally friendly condition-based microgap discharge.
2008 Dec
Ruthenium complexes with vinyl, styryl, and vinylpyrenyl ligands: a case of non-innocence in organometallic chemistry.
2008 Jan 9
Synthesis and characterization of polyacetylene with side-chain thiophene functionality.
2008 Mar
Spectroscopic observation of the resonance-stabilized 1-phenylpropargyl radical.
2008 Mar 12
Mechanistic variety in zirconium-catalyzed bond-forming reaction of arsines.
2008 Sep 7
Trisulfonated porphyrazines: new photosensitizers for the treatment of retinal and subretinal edema.
2009 Jul 23
4-Butyl-1-(2,3,4-tri-O-acetyl-β-l-fuco-pyranos-yl)-1H-1,2,3-triazole.
2009 Jul 25
Competition between cluster fragmentation, C-C bond coupling and C-X bond activation in silver hexynyl cluster cations, [(C(4)H(9)CCAg)(n)Ag](+). Size does matter!
2009 Jun 7
Palladium-catalyzed cross coupling reactions of 4-bromo-6H-1,2-oxazines.
2009 Sep 16
Organozirconium complexes as catalysts for Markovnikov-selective intermolecular hydrothiolation of terminal alkynes: scope and mechanism.
2010 Aug 4
Synthesis of 2a,8b-Dihydrocyclobuta[a]naphthalene-3,4-diones.
2010 Jul 13
Structure-activity relationships of mono-substituted trisulfonated porphyrazines for the photodynamic therapy (PDT) of cancer.
2010 Mar
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:33:09 GMT 2023
Edited
by admin
on Fri Dec 15 19:33:09 GMT 2023
Record UNII
5FZF2F38F5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1-Hexyne
Systematic Name English
Butylacetylene
Common Name English
NSC-9709
Code English
n-Butylacetylene
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID30870753
Created by admin on Fri Dec 15 19:33:09 GMT 2023 , Edited by admin on Fri Dec 15 19:33:09 GMT 2023
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NSC
9709
Created by admin on Fri Dec 15 19:33:09 GMT 2023 , Edited by admin on Fri Dec 15 19:33:09 GMT 2023
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PUBCHEM
12732
Created by admin on Fri Dec 15 19:33:09 GMT 2023 , Edited by admin on Fri Dec 15 19:33:09 GMT 2023
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ECHA (EC/EINECS)
211-736-9
Created by admin on Fri Dec 15 19:33:09 GMT 2023 , Edited by admin on Fri Dec 15 19:33:09 GMT 2023
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CAS
693-02-7
Created by admin on Fri Dec 15 19:33:09 GMT 2023 , Edited by admin on Fri Dec 15 19:33:09 GMT 2023
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CAS
26856-30-4
Created by admin on Fri Dec 15 19:33:09 GMT 2023 , Edited by admin on Fri Dec 15 19:33:09 GMT 2023
NON-SPECIFIC SUBSTITUTION
WIKIPEDIA
1-Hexyne
Created by admin on Fri Dec 15 19:33:09 GMT 2023 , Edited by admin on Fri Dec 15 19:33:09 GMT 2023
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FDA UNII
5FZF2F38F5
Created by admin on Fri Dec 15 19:33:09 GMT 2023 , Edited by admin on Fri Dec 15 19:33:09 GMT 2023
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