| Weight | 66.103 g/mol |
|---|---|
| Formula | C5H6 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Cyclopropylacetylene (6746-94-7)
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- Synthesis and Evaluation of Efavirenz (SustivaTM) Analogues as HIV-1 Reverse Transcriptase Inhibitors: Replacement of the Cyclopropylacetylene Side Chain (Bioorganic & Medicinal Chemistry Letters, 2001)
- Microwave structures of cyanocyclopropane and cyclopropylacetylene. Effects of cyclopropyl .pi. conjugation on structure (Journal of the American Chemical Society, 1983)
- Free-radical selenosulfonation of vinylcyclopropanes, a cyclopropylidene, and cyclopropylacetylene. Relative rates of chain-transfer, ring-opening, and inversion in radical intermediates (Journal of Organic Chemistry, 1989)
- Addition to halogens to cyclopropylacetylene (Journal of Organic Chemistry, 1978)
- Molecular structure of cyclopropylacetylene as determined by a combined analysis of electron diffraction and microwave spectroscopic data (The Journal of Physical Chemistry, 1983)
- Efficient synthesis of cyclopropylacetylene (1998)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H225: Highly Flammable liquid and vapor
Danger Flammable liquids - Category 2 - H318: Causes serious eye damage
Danger Serious eye damage/eye irritation - Category 1 -
SMILESC#CC1CC1
-
InChIKeyNPTDXPDGUHAFKC-UHFFFAOYSA-N
- Pubchem - Cyclopropylacetylene
- Wikipedia - Cyclopropylacetylene
Cyclopropylacetylene is an organic compound with the chemical formula C 5H 6. Under normal conditions, the substance is a clear, flammable liquid. Cyclopropylacetylene is used as an important reagent to synthesize pharmaceuticals and other organic compounds.
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