Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H8 |
| Molecular Weight | 68.117 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC#CC
InChI
InChIKey=NKTDTMONXHODTI-UHFFFAOYSA-N
InChI=1S/C5H8/c1-3-5-4-2/h3H2,1-2H3
| Molecular Formula | C5H8 |
| Molecular Weight | 68.117 |
| 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 |
|---|---|---|
| Considering Fe(II/IV) redox processes as mechanistically relevant to the catalytic hydrogenation of olefins by [PhBP iPr 3]Fe-H x species. | 2004 Nov 15 |
|
| Gold-catalyzed [4C+3C] intramolecular cycloaddition of allenedienes: synthetic potential and mechanistic implications. | 2009 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:31:29 GMT 2023
by
admin
on
Fri Dec 15 18:31:29 GMT 2023
|
| Record UNII |
57NG6HKI9D
|
| Record Status |
Validated (UNII)
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| Record Version |
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627-21-4
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2-Pentyne
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12310
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210-989-2
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57NG6HKI9D
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DTXSID80211758
Created by
admin on Fri Dec 15 18:31:29 GMT 2023 , Edited by admin on Fri Dec 15 18:31:29 GMT 2023
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