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(6-Oxobicyclo[2.2.1]heptan-2-yl)methyl acetate

Base Information
  • Chemical Name:(6-Oxobicyclo[2.2.1]heptan-2-yl)methyl acetate
  • CAS No.:81523-34-4
  • Molecular Formula:C10H14O3
  • Molecular Weight:182.219
  • Hs Code.:
  • NSC Number:134989
  • DSSTox Substance ID:DTXSID901002024
(6-Oxobicyclo[2.2.1]heptan-2-yl)methyl acetate

Synonyms:81523-34-4;NSC134989;(6-oxobicyclo[2.2.1]heptan-2-yl)methyl acetate;SCHEMBL9593536;DTXSID901002024;NSC-134989

Suppliers and Price of (6-Oxobicyclo[2.2.1]heptan-2-yl)methyl acetate
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 4 raw suppliers
Chemical Property of (6-Oxobicyclo[2.2.1]heptan-2-yl)methyl acetate
Chemical Property:
  • Vapor Pressure:0.00797mmHg at 25°C 
  • Boiling Point:267.8°Cat760mmHg 
  • Flash Point:114°C 
  • Density:1.144g/cm3 
  • XLogP3:0.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:182.094294304
  • Heavy Atom Count:13
  • Complexity:247
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=O)OCC1CC2CC1C(=O)C2
Technology Process of (6-Oxobicyclo[2.2.1]heptan-2-yl)methyl acetate

There total 7 articles about (6-Oxobicyclo[2.2.1]heptan-2-yl)methyl acetate 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:
Multi-step reaction with 4 steps
1: 78 percent / diethyl ether / Ambient temperature
2: 92 percent / p-toluenesulfonic acid / benzene / 6 h / Heating
3: 1.) lithium aluminum hydride, 2.) hydrochloric acid / 1.) ether, 4 h, 2.) room temperature, 3 h
4: 84 percent / pyridine / Ambient temperature
With hydrogenchloride; lithium aluminium tetrahydride; toluene-4-sulfonic acid; In pyridine; diethyl ether; benzene;
DOI:10.1021/ja00378a033
Guidance literature:
Multi-step reaction with 4 steps
1: 73 percent / iodine, triethylamine / methanol / 48 h / Heating
2: 8 percent Chromat. / diethyl ether / 4 h / Irradiation
3: 73 percent Chromat. / sulfuric acid / 2.5 h / Ambient temperature
4: 84 percent / pyridine / Ambient temperature
With sulfuric acid; iodine; triethylamine; In pyridine; methanol; diethyl ether;
DOI:10.1021/ja00378a033
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