Tert-butyl 1-aminocyclopentane-1-carboxylate

Base Information

Chemical Name:Tert-butyl 1-aminocyclopentane-1-carboxylate
CAS No.:120225-90-3
Molecular Formula:C₁₀H₁₉NO₂
Molecular Weight:185.266
Hs Code.:
European Community (EC) Number:829-268-4
Mol file:120225-90-3.mol

Synonyms:120225-90-3;tert-butyl 1-aminocyclopentane-1-carboxylate;tert-butyl 1-aminocyclopentanecarboxylate;Cyclopentanecarboxylic acid, 1-amino-, 1,1-dimethylethyl ester (9CI);C10H19NO2;SCHEMBL3295142;KTYIEPAXQWLADO-UHFFFAOYSA-N;Cyclopentanecarboxylic acid, 1-amino-, 1,1-dimethylethyl ester;VEA22590;AKOS010133600;tert-butyl1-aminocyclopentanecarboxylate;CS-0261882;EN300-80384;F78801;1-aminocyclopentane carboxylic acid t-butyl ester;cyclopentanecarboxylic acid,1-amino-,tert-butyl ester

Suppliers and Price of Tert-butyl 1-aminocyclopentane-1-carboxylate

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

AK Scientific
Tert-butyl1-aminocyclopentane-1-carboxylate
2.5g
$ 1016.00

Acrotein
tert-butyl1-aminocyclopentanecarboxylate 97%
5g
$ 916.67

Total 8 raw suppliers

Chemical Property of Tert-butyl 1-aminocyclopentane-1-carboxylate

Chemical Property:

Boiling Point:235.4±23.0 °C(Predicted)
PKA:8.10±0.20(Predicted)
PSA：29.10000
Density:1.018±0.06 g/cm3(Predicted)
LogP:0.47120
XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:185.141578849
Heavy Atom Count:13
Complexity:200

Purity/Quality:

97% ^*data from raw suppliers

Tert-butyl1-aminocyclopentane-1-carboxylate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)C1(CCCC1)N

Technology Process of Tert-butyl 1-aminocyclopentane-1-carboxylate

There total 1 articles about Tert-butyl 1-aminocyclopentane-1-carboxylate 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: