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Chloroacetyl chloride-1-13C

Base Information
  • Chemical Name:Chloroacetyl chloride-1-13C
  • CAS No.:159301-42-5
  • Molecular Formula:C2H2Cl2O
  • Molecular Weight:113.932
  • Hs Code.:
  • European Community (EC) Number:687-240-5
  • DSSTox Substance ID:DTXSID70479981
  • Wikidata:Q82314414
  • Mol file:159301-42-5.mol
Chloroacetyl chloride-1-13C

Synonyms:Chloroacetyl chloride-1-13C;159301-42-5;SCHEMBL1331137;DTXSID70479981;Chloroacetyl chloride-1-13C, 99 atom % 13C

Suppliers and Price of Chloroacetyl chloride-1-13C
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • ChloroacetylChloride-13C
  • 100mg
  • $ 185.00
  • American Custom Chemicals Corporation
  • CHLOROACETYL CHLORIDE-1-13C 95.00%
  • 5MG
  • $ 503.47
Total 1 raw suppliers
Chemical Property of Chloroacetyl chloride-1-13C
Chemical Property:
  • PSA:17.07000 
  • LogP:0.99060 
  • XLogP3:1.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:112.9516249
  • Heavy Atom Count:5
  • Complexity:42.9
Purity/Quality:

ChloroacetylChloride-13C *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C(C(=O)Cl)Cl
  • Isomeric SMILES:C([13C](=O)Cl)Cl
  • Uses Chloroacetyl Chloride-13C is isotope labelled Chloroacetyl Chloride, is a versatile building block used for the construction of various chemical compounds. It can be used for the synthesis of novel Inulin (I666680) derivatives with chlorinated benzene having antifungal activity.
Technology Process of Chloroacetyl chloride-1-13C

There total 2 articles about Chloroacetyl chloride-1-13C which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With thionyl chloride; at 76 ℃; for 4h;
DOI:10.1021/es950423e
Guidance literature:
With hydrogenchloride; N-chloro-succinimide; thionyl chloride; acetic acid; Yield given. Multistep reaction; 1.) 70 deg C, 30 min, 2.) 85 deg C, 90 min;
DOI:10.1002/jlcr.2580340908
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