| Weight | 68.119 g/mol |
|---|---|
| Formula | C5H8 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
1-PENTYNE (627-19-0)
Score:
#2360 in Physics
,
#7216 in Chemistry
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- Chemical Selection of Mutants That Affect Alcohol Dehydrogenase in Drosophila II. Use of 1PENTYNE3Ol (Genetics, 1975)
- Extension of Sugar Chains through Acetylenic Intermediates. IV Derivatives of 1-pentyne-D-erythro(andD-threo)-3,4,5-triol (Journal of Organic Chemistry, 1968)
- MECHANISM-BASED INACTIVATION OF CYTOCHROMES P450 2E1 AND 2B1 BY 5-PHENYL-1-PENTYNE (Archives of Biochemistry and Biophysics, 1998)
- Rotational Isomerism in 1Pentyne from the Microwave Spectrum (Journal of Chemical Physics, 1972)
- Hydrosilylation of 1-Pentyne by Triethylsilane Catalyzed by Phosphine-Rhodium Complexes (Journal of Organometallic Chemistry, 1981)
- Highly permeable poly(4-methyl-1-pentyne)/NH2-MIL 53 (Al) mixed matrix membrane for CO2/CH4 separation (RSC Advances, 2014)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCCC#C
-
InChIKeyIBXNCJKFFQIKKY-UHFFFAOYSA-N
- Pubchem - 1-PENTYNE
- Wikipedia - 1-Pentyne
1-Pentyne, an organic compound, is a terminal alkyne. It is an isomer of 2-pentyne, an internal alkyne.
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1-PENTYNE
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