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8-Chlorochroman

Base Information
  • Chemical Name:8-Chlorochroman
  • CAS No.:3722-69-8
  • Molecular Formula:C9H9ClO
  • Molecular Weight:168.623
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30697780
  • Nikkaji Number:J3.665.819C
  • Mol file:3722-69-8.mol
8-Chlorochroman

Synonyms:8-Chlorochroman;3722-69-8;8-Chloro-3,4-dihydro-2H-1-benzopyran;8-chloro-3,4-dihydro-2H-chromene;SCHEMBL15319473;DTXSID30697780;CYSQTUPJQFEKES-UHFFFAOYSA-N;MFCD03695452;AKOS006279204;DS-3275;CS-0155312;J3.665.819C;N10904

Suppliers and Price of 8-Chlorochroman
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
Total 8 raw suppliers
Chemical Property of 8-Chlorochroman
Chemical Property:
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:168.0341926
  • Heavy Atom Count:11
  • Complexity:138
Purity/Quality:

98%Min *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CC2=C(C(=CC=C2)Cl)OC1
Technology Process of 8-Chlorochroman

There total 6 articles about 8-Chlorochroman 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 di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 ℃; for 15h; Inert atmosphere;
Guidance literature:
With Co(dmgBF2)2(CH3CN)2; 3-cyano-N-methyl-quinolinium perchlorate; In acetonitrile; at 20 ℃; Overall yield = 68 %; regioselective reaction; Sealed tube; Inert atmosphere; Irradiation; High pressure;
DOI:10.1021/acs.orglett.7b00463
Guidance literature:
Multi-step reaction with 2 steps
1.1: borane-THF / tetrahydrofuran / 15 h / 20 °C
1.2: 1.75 h / 20 °C
2.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 15 h / 0 °C / Inert atmosphere
With borane-THF; di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran;
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