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| SKU | Size | Availability |
Price | Qty |
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P466781-100ml
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100ml |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
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$331.90
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| Synonyms | DTXSID4060789 | EINECS 210-856-9 | PROPARGYL CHLORIDE [MI] | 3-Chloropropyne | 3-Chloroprop-1-yne (Propargyl chloride) | Propargyl chloride | P0810 | 1-Propyne, 3-chloro- | 3-CHLORO-1-PROPYNE | EN300-119441 | Q420202 | A833787 | 3-chloranylprop-1-yne | CH |
|---|---|
| Specifications & Purity | 70wt. % in toluene |
| Storage Temp | Store at 2-8°C |
| Shipped In |
Wet ice This product requires cold chain shipping. Ground and other economy services are not available. |
| Product Description |
Description Product is the 70wt.% solution of propargyl chloride in toluene. Propargyl chloride is a propargyl halide. Its trimethylsilylation reaction has been reported. Liquid-phase Raman spectra, and vapor-phase and solution-phase infrared spectra of propargyl chloride has been studied at 100-3400cm-1and 300-3800cm-1, respectively. It participates in the addition reaction with acyclic 1,3-dienes (at -78°C) in the presence of zinc chloride.Propargyl chloride solution may be used for the enantioselective synthesis of enantiomerically enriched homopropargyl alcohols.Propargyl chloride may be used as propargylating agent in the preparation of arabinogalactan propargyl ethers with degree of substitution up to 1.8. It may be used for thein situpreparation of propargyltrichlorosilane and allenyltrichlorosilane, required for the synthesis of optically active allenic and homopropargylic alcohols. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Acetylides |
| Class | Not available |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Acetylides |
| Alternative Parents | Organochlorides Hydrocarbon derivatives Alkyl chlorides |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Acetylide - Hydrocarbon derivative - Organochloride - Organohalogen compound - Alkyl halide - Alkyl chloride - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as acetylides. These are compounds arising by replacement of one or both hydrogen atoms of acetylene (ethyne) by a metal or other cationic group. E.g. NaC#CH monosodium acetylide. By extension, analogous compounds derived from terminal acetylenes, RC#CH. The class is limited here to derivatives of acetylene where the hydrogen atom is replaced with an element with similar or lower electronegativity that carbon. |
| External Descriptors | Not available |
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| IUPAC Name | 3-chloroprop-1-yne |
|---|---|
| INCHI | InChI=1S/C3H3Cl/c1-2-3-4/h1H,3H2 |
| InChIKey | LJZPPWWHKPGCHS-UHFFFAOYSA-N |
| Smiles | C#CCCl |
| Isomeric SMILES | C#CCCl |
| WGK Germany | 2 |
| Molecular Weight | 74.51 |
| Beilstein | 506005 |
| Reaxy-Rn | 506005 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506005&ln= |
| Refractive Index | 1.44 |
|---|---|
| Flash Point(°F) | 66.2 °F |
| Flash Point(°C) | 19 °C |
| Boil Point(°C) | 57 °C |
| Melt Point(°C) | -78 °C |
| Molecular Weight | 74.510 g/mol |
| XLogP3 | 0.900 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 0 |
| Exact Mass | 73.9923 Da |
| Monoisotopic Mass | 73.9923 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 4 |
| Formal Charge | 0 |
| Complexity | 38.500 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |