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(E)-hept-2-enoyl chloride

Base Information
  • Chemical Name:(E)-hept-2-enoyl chloride
  • CAS No.:76875-23-5
  • Molecular Formula:C7H11ClO
  • Molecular Weight:146.617
  • Hs Code.:2916190090
  • European Community (EC) Number:673-233-4
  • Nikkaji Number:J2.981.352C
  • Wikidata:Q76310610
  • Mol file:76875-23-5.mol
(E)-hept-2-enoyl chloride

Synonyms:(E)-hept-2-enoyl chloride;76875-23-5;(E)-Hept-2-enoylchloride;(2E)-hept-2-enoyl chloride;hept-2-enoyl chloride;2-Heptenoic acid chloride;trans-2-heptenoyl chloride;SCHEMBL1569414;REDBNPUNYZYECN-AATRIKPKSA-N;AKOS006278408

Suppliers and Price of (E)-hept-2-enoyl chloride
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
  • Crysdot
  • (E)-Hept-2-Enoylchloride 95+%
  • 5g
  • $ 636.00
  • American Custom Chemicals Corporation
  • (2E)-HEPT-2-ENOYL CHLORIDE 95.00%
  • 5MG
  • $ 503.45
  • AHH
  • (E)-Hept-2-enoylchloride 98%
  • 10g
  • $ 830.00
Total 6 raw suppliers
Chemical Property of (E)-hept-2-enoyl chloride
Chemical Property:
  • Boiling Point:59-60 °C(Press: 6 Torr) 
  • PSA:17.07000 
  • Density:1.002±0.06 g/cm3(Predicted) 
  • LogP:2.49820 
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:4
  • Exact Mass:146.0498427
  • Heavy Atom Count:9
  • Complexity:108
Purity/Quality:

98%min *data from raw suppliers

(E)-Hept-2-Enoylchloride 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCC=CC(=O)Cl
  • Isomeric SMILES:CCCC/C=C/C(=O)Cl
Technology Process of (E)-hept-2-enoyl chloride

There total 3 articles about (E)-hept-2-enoyl chloride 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; In N,N-dimethyl-formamide; for 1.5h; Heating;
DOI:10.1002/hlca.19850680533
Guidance literature:
Multi-step reaction with 2 steps
1: 71 percent / pyridine
2: thionyl chloride / CH2Cl2 / 1 h / Heating
With pyridine; thionyl chloride; In dichloromethane;
DOI:10.1021/ol9910565
Guidance literature:
Multi-step reaction with 2 steps
1: 45 percent
2: 78 percent / SOCl2 / dimethylformamide / 1.5 h / Heating
With thionyl chloride; In N,N-dimethyl-formamide;
DOI:10.1002/hlca.19850680533
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