| Weight | 76.526 g/mol |
|---|---|
| Formula | C3H5Cl |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1-Chloropropene
590-21-6, 16136-85-9, 36472-34-1, 16136-84-8
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- Ab initio heats of formation for chlorinated hydrocarbons: Allyl chloride, cis- and trans-1-chloropropene, and vinyl chloride (Journal of Chemical Physics, 1997)
- Reactions of triphenylsilyllithium with 1-chloropropene and 1-chloro-1-butene (Journal of Organometallic Chemistry, 1964)
- Raman and infrared spectra, vibrational assignments and barriers to internal rotation of cis- and trans-1-chloropropene (Journal of Raman Spectroscopy, 1982)
- Cycloaddition. XVII. Twelve products of photosensitized addition of 1-chloropropene to cyclopentadiene (Journal of Organic Chemistry, 1975)
- The reaction of guanine with some potential metabolites of 1-chloropropene (Tetrahedron Letters, 1979)
- DIMETHYL 3-CHLOROPROPENE-2-PHOSPHONATE 1. SYNTHESIS THROUGH OXIDATIVE CHLOROPHOSPHORYLATION OF ALLYL CHLORIDE (Phosphorus Sulfur and Silicon and The Related Elements, 1995)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC=CCl
-
InChIKeyOWXJKYNZGFSVRC-UHFFFAOYSA-N
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Alternate Names
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Synthesis
4-chloro-3,4-dimethyl-2-pentanone
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
Similar Compounds
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(590-21-6, 16136-84-8)
1 alternate name
3 suppliers
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(590-21-6, 36472-34-1, 16136-84-8)
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(107-30-2)
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(352-93-2, 68990-36-3)
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(75-29-6)
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(109-68-2, 58718-78-8, 68956-55-8, 627-20-3, 646-04-8)
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(29656-63-1, 543-59-9)
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(693-07-2)
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(68956-55-8, 109-68-2, 627-20-3)
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butyraldehyde
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(513-37-1)
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(115-11-7, 68037-14-9)
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(928-96-1, 544-12-7)
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2-(Methylamino)ethanol
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CYCLOPROPANE
(75-19-4)
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(75-33-2)
1 alternate name
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1-PENTENE
(109-67-1, 25377-72-4, 68814-91-5)
1 alternate name
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Acetaldoxime
(107-29-9, 5780-37-0)
1 alternate name
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1,2-DIETHYLHYDRAZINE
(1615-80-1)
1 alternate name
1 safety hazard
3 suppliers
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