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
SMILES
CCC#CCC
InChI
InChIKey=DQQNMIPXXNPGCV-UHFFFAOYSA-N
InChI=1S/C6H10/c1-3-5-6-4-2/h3-4H2,1-2H3
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
Title | Date | PubMed |
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Experimental Raman spectra of dilute and laser-light-sensitive [Rh(4)(CO)(9)(mu-CO)(3)] and [(mu(4)-eta(2)-3-hexyne)Rh(4)(CO)(8)(mu-CO)(2)]. Comparison with theoretically predicted spectra. | 2006 Sep 21 |
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Alkyne as a spectator ligand for the nickel-catalyzed multicomponent connection reaction of diphenylzinc, 1,3-butadiene, aldehydes, and amines. | 2007 May 10 |
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Synthetic, mechanistic, and computational investigations of nitrile-alkyne cross-metathesis. | 2008 Jul 16 |
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Mesityl alkyne substituents for control of regiochemistry and reversibility in zirconocene couplings: new synthetic strategies for unsymmetrical zirconacyclopentadienes and conjugated polymers. | 2009 Apr 8 |
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Gold(I) chloride coordinated 3-hexyne. | 2009 Jan 19 |
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Synthesis and reactivity of metal carbene complexes with heterobiaryl spacer substituents. | 2009 Jan 28 |
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Si3C2-rings: from a nonconjugated trisilacyclopentadiene to an aromatic trisilacyclopentadienide and cyclic disilenide. | 2009 May 13 |
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Preparation of imidazolin-2-iminato molybdenum and tungsten benzylidyne complexes: a new pathway to highly active alkyne metathesis catalysts. | 2010 Aug 2 |
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Alkoxydienes via copper-promoted couplings: utilizing an alkyne effect. | 2010 Jun 4 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:37:13 GMT 2023
by
admin
on
Fri Dec 15 19:37:13 GMT 2023
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Record UNII |
9GTQ990Q4K
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Record Status |
Validated (UNII)
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Record Version |
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928-49-4
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13568
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DTXSID30239144
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9GTQ990Q4K
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3-Hexyne
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213-173-4
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