7-Oxabicyclo[2.2.1]heptane-2-carboxylic acid

Base Information

Chemical Name:7-Oxabicyclo[2.2.1]heptane-2-carboxylic acid
CAS No.:19800-01-2
Molecular Formula:C7H10O3
Molecular Weight:142.155
Hs Code.:
European Community (EC) Number:826-886-6,828-234-6
DSSTox Substance ID:DTXSID90545051
Nikkaji Number:J2.501.389A

Synonyms:7-OXABICYCLO[2.2.1]HEPTANE-2-CARBOXYLIC ACID;19800-01-2;7-oxa-bicyclo[2.2.1]heptane-2-carboxylic acid;C7H10O3;rac-(1R,2S,4S)-7-oxabicyclo[2.2.1]heptane-2-carboxylic acid;1034079-37-2;38263-55-7;38263-56-8;7-Oxabicyclo(2.2.1)heptane-2-carboxylic acid;SCHEMBL2969767;DTXSID90545051;UYLYISCHTFVYHN-UHFFFAOYSA-N;MFCD18838957;AKOS006381607;AB86071;AB86122;AB86336;BS-13331;CS-0099964;EN300-77106;F51361;7-OXABICYCLO[2.2.1]HEPTANE-2-CARBOXYLICACID

Suppliers and Price of 7-Oxabicyclo[2.2.1]heptane-2-carboxylic acid

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 7-Oxabicyclo[2.2.1]heptane-2-carboxylic acid

Chemical Property:

XLogP3:0.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:142.062994177
Heavy Atom Count:10
Complexity:166

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CC2C(CC1O2)C(=O)O

Technology Process of 7-Oxabicyclo[2.2.1]heptane-2-carboxylic acid

There total 3 articles about 7-Oxabicyclo[2.2.1]heptane-2-carboxylic acid 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:

Reference yield: 89.0%

: 90760-56-8
(-)-7-endo-oxabicyclo<2.2.1>hept-5-ene-2-carboxylic acid

: 19800-01-2,38263-55-7,38263-56-8,64589-27-1
endo-2-Carboxy-7-oxabicyclo<2.2.1>heptan

Guidance literature:: With hydrogen; palladium on activated charcoal;
DOI:10.1039/c39860000771

Reference yield:

: 19800-01-2,38263-55-7,38263-56-8,64589-27-1
endo-2-Carboxy-7-oxabicyclo<2.2.1>heptan

Guidance literature:: endo-2-Carboxy-7-oxabicyclo<2.2.1>hepten-(5), H2/Pd/C;
DOI:10.1021/ja00880a030

Reference yield:

: 19800-01-2,38263-55-7,38263-56-8,64589-27-1
endo-2-Carboxy-7-oxabicyclo<2.2.1>heptan

Guidance literature:: Mischg. von endo- u. exo-2-Carbomethoxy-7-oxabicyclo<2.2.1>heptan (13 u. 14), wss. Na-Hydroxid (neben d. exo-Isomeren 12);
DOI:10.1021/jm00290a007