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Propargyl chloride solution - 70wt. % in toluene, high purity , CAS No.624-65-7

    Grade & Purity:
  • 70wt. % in toluene
In stock
Item Number
P466781
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Price Qty
P466781-100ml
100ml
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$331.90

Basic Description

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.

Taxonomic Classification

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

Names and Identifiers

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=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

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

Citations of This Product

1. Zixuan Xu, Ke Liu, He Huang, Yadong Zhang, Zhouyang Long, Minman Tong, Guojian Chen.  (2022)  Quaternization-induced catalyst-free synthesis of viologen-linked ionic polyacetylenes towards heterogeneous catalytic CO2 fixation.  Journal of Materials Chemistry A,  10  (10): (5540-5549). 
2. Lingxiao Gu, Qingquan Xue, Shusen Peng, Gang Wang, Jin Han, Xuedong Wu.  (2016)  A novel and facile strategy to inhibit corrosion: thiol-click synthesis of polythiols and their skinning on a metal surface to form super thick protective films.  Polymer Chemistry,  (3): (625-632). 
3. Yujing Zuo, Dengxu Wang, Jie Zhang, Shengyu Feng.  (2014)  Multifunctional alkoxysilanes prepared by thiol–yne “click” chemistry: their luminescence properties and modification on a silicon surface.  RSC Advances,  (108): (62827-62834). 
4. Daoyi Jiang, Gang Wang, Feng Zheng, Jin Han, Xuedong Wu.  (2014)  Novel thermo-sensitive hydrogels containing polythioether dendrons: facile tuning of LCSTs, strong absorption of Ag ions, and embedment of smaller Ag nanocrystals.  Polymer Chemistry,  (4): (625-632). 
5. Jin Han, Bo Zhao, Aijin Tang, Yanqin Gao, Chao Gao.  (2012)  Fast and scalable production of hyperbranched polythioether-ynes by a combination of thiol-halogen click-like coupling and thiol-yne click polymerization.  Polymer Chemistry,  (7): (1918-1925). 

Solution Calculators

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