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Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, ethyl ester

Base Information
  • Chemical Name:Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, ethyl ester
  • CAS No.:10138-32-6
  • Molecular Formula:C10H14O2
  • Molecular Weight:166.22
  • Hs Code.:2916209090
  • NSC Number:62714,26489
  • DSSTox Substance ID:DTXSID30884451
  • Nikkaji Number:J41.837D
  • Mol file:10138-32-6.mol
Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, ethyl ester

Synonyms:10138-32-6;ETHYL BICYCLO[2.2.1]HEPT-5-ENE-2-CARBOXYLATE;Ethyl 5-norbornene-2-carboxylate;Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, ethyl ester;5-Norbornene-2-carboxylic acid, ethyl ester;NSC 26489;UNII-QEA96R4A1Z;2,5-Endomethylene-3-cyclohexene carboxylic acid, ethyl ester;BICYCLO(2.2.1)HEPT-5-ENE-2-CARBOXYLIC ACID, ETHYL ESTER;WLN: L55 A CUTJ FVO2;ethyl bicyclo[2.2.1]hept-2-ene-5-carboxylate;NSC26489;NCIOpen2_000131;QEA96R4A1Z;2-ethoxycarbonyl-5-norbornene;SCHEMBL200507;DTXSID30884451;NSC62714;NSC-26489;NSC-62714;AKOS015917768;AC-4862;AS-75467;LS-43706;FT-0766049;Norborna-2-ene-5-carboxylic acid ethyl ester;E77868;J-650254;bicyclo[2.2.1]hept-5-ene-2-carboxylic acid ethyl ester;Ethyl (1S,2S,4S)-bicyclo[2.2.1]hept-5-ene-2-carboxylate

Suppliers and Price of Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, ethyl ester
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
  • Ethylbicyclo[2.2.1]hept-5-ene-2-carboxylate 97%
  • 10g
  • $ 60.00
  • Chemenu
  • ethylbicyclo[2.2.1]hept-5-ene-2-carboxylate 97%
  • 100g
  • $ 337.00
  • American Custom Chemicals Corporation
  • ETHYL-5-NORBORNENE-2-CARBOXYLATE 95.00%
  • 1G
  • $ 686.88
  • Ambeed
  • Ethylbicyclo[2.2.1]hept-5-ene-2-carboxylate 98%
  • 500g
  • $ 729.00
  • Ambeed
  • Ethylbicyclo[2.2.1]hept-5-ene-2-carboxylate 98%
  • 100g
  • $ 223.00
  • Ambeed
  • Ethylbicyclo[2.2.1]hept-5-ene-2-carboxylate 98%
  • 25g
  • $ 65.00
  • Ambeed
  • Ethylbicyclo[2.2.1]hept-5-ene-2-carboxylate 98%
  • 5g
  • $ 18.00
Total 36 raw suppliers
Chemical Property of Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, ethyl ester
Chemical Property:
  • Vapor Pressure:0.142mmHg at 25°C 
  • Refractive Index:1.508 
  • Boiling Point:216.164 °C at 760 mmHg 
  • Flash Point:75.303 °C 
  • PSA:26.30000 
  • Density:1.089 g/cm3 
  • LogP:1.76170 
  • XLogP3:1.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:166.099379685
  • Heavy Atom Count:12
  • Complexity:220
Purity/Quality:

99%, *data from raw suppliers

Ethylbicyclo[2.2.1]hept-5-ene-2-carboxylate 97% *data from reagent suppliers

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

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CCOC(=O)C1CC2CC1C=C2
Technology Process of Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, ethyl ester

There total 18 articles about Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, ethyl ester 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 lithium perchlorate; In diethyl ether; for 5h; Product distribution; Ambient temperature; other dienes and dienophiles; other solvents, temp., and reaction times;
DOI:10.1021/ja00167a096
Guidance literature:
With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at -78 - -5 ℃; for 3h; Product distribution; Mechanism; other 1,3-dienes, var. conditions;
DOI:10.1021/jo00245a058
Guidance literature:
With lithium aluminium tetrahydride; In tetrahydrofuran; dichloromethane; at 0 - 20 ℃; for 3h; Cooling with ice; Inert atmosphere;
DOI:10.1055/s-0031-1290485
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