1-Boc-4-(aminomethyl)piperidine

Base Information Edit

Chemical Name:1-Boc-4-(aminomethyl)piperidine
CAS No.:144222-22-0
Molecular Formula:C11H22N2O2
Molecular Weight:214.308
Hs Code.:29339900
European Community (EC) Number:672-194-0
DSSTox Substance ID:DTXSID10353110
Nikkaji Number:J495.255C
Wikidata:Q72448257
Mol file:144222-22-0.mol

Synonyms:144222-22-0;1-Boc-4-(aminomethyl)piperidine;tert-butyl 4-(aminomethyl)piperidine-1-carboxylate;1-Boc-4-Aminomethylpiperidine;1-Boc-4-aminomethyl-piperidine;4-(Aminomethyl)-1-N-Boc-piperidine;4-aminomethyl-1-n-(t-butoxycarbonyl)piperidine;1-n-boc-4-(aminomethyl)piperidine;boc-4-(aminomethyl)-piperidine;4-aminomethyl-piperidine-1-carboxylic acid tert-butyl ester;MFCD01076207;N-Boc-4-(aminomethyl)piperidine;4-(aminomethyl)-1-BOC-piperidine;1-Piperidinecarboxylic acid, 4-(aminomethyl)-, 1,1-dimethylethyl ester;1-Boc-4-aminomethyl-piperidine, HCl;4-(aminomethyl)-1-tert-butoxycarbonylpiperidine;tert-butyl 4-(aminomethyl)-1-piperidinecarboxylate;1,1-dimethylethyl 4-(aminomethyl)-1-piperidinecarboxylate;4-Aminomethylpiperidine-1-carboxylic acid tert-butyl ester;4-Aminomethyl-1-Boc-piperidine;1-tert-Butoxycarbonyl-4-aminomethylpiperidine;tert-Butyl 4-aminomethylpiperidine-1-carboxylate;4-(aminomethyl)-1-(tert-butoxycarbonyl)piperidine;SCHEMBL103083;4-aminomethyl-N-Boc-piperidine;N-Boc-4-aminomethyl piperidine;4-(Aminomethyl)-Boc-piperidine;1-N-Boc-4-aminomethylpiperidine;DTXSID10353110;KLKBCNDBOVRQIJ-UHFFFAOYSA-N;1-boc-4-(aminomethyl)-piperidine;4-(Aminomethyl)-1-piperidinecarboxylic Acid tert-Butyl Ester;N-Boc-4-(aminomethyl)-piperidine;BCP22304;CS-B0408;4-(aminomethyl)-1-N-Boc piperidine;STK503785;AKOS005146254;DS-0462;PS-6021;1-Boc-4-(aminomethyl)piperidine, 97%;BP-11083;HY-40007;SY007891;4-aminomethyl-1-t-butoxycarbonylpiperidine;(1-t-Butoxycarbonyl-4-piperidyl)methylamine;1-t-butoxycarbonyl-4-(aminomethyl)piperidine;1-t-butyloxycarbonyl-4-aminomethylpiperidine;4-Aminomethyl-1-tert-butoxycarbonylpiperidine;AM20080335;B4445;BB 0254286;FT-0601662;N-tert-butoxycarbonyl-4-aminomethylpiperidine;(1-t-butoxycarbonyl-4-piperidyl)me-thylamine;EN300-40882;1-(tert-Butoxycarbonyl)-4-aminomethylpiperidine;1-tert-Butoxycarbonyl-4-(aminomethyl)piperidine;4-aminomethyl-1-(tert-butoxycarbonyl)piperidine;4-Aminomethyl-1-tert-butyloxycarbonylpiperidine;N-(tert-Butoxycarbonyl)-4-aminomethylpiperidine;N-(tert-butoxycarbonyl)4-aminomethyl piperidine;(1-tert-Butoxycarbonylpiperidin-4-yl)methylamine;1-(tert-butoxycarbonyl)-4(aminomethyl)piperidine;1-(tert-butoxycarbonyl)piperidin-4-ylmethylamine;N-tert-butyloxycarbonyl-4-(aminomethyl)piperidine;N-tert-butyloxycarbonyl4-(aminomethyl)piperidine;tert-butyl 4-(aminomethyl)piperidine-carboxylate;tert-butyl 4-aminomethyl-1-piperidinecarboxylate;1-(t-butyloxycarbonyl)-4-(aminomethyl)piperidine;1-(tert-butoxycarbonyl)-4-(aminomethyl)piperidine;1-(tert-butoxycarbonyl)piperidine-4-ylmethylamine;1-tert-Butyloxycarbonyl-4-(aminomethyl)piperidine;tert-butyl-4-(aminomethyl)piperidine-1-carboxylate;[(1-tert-butoxycarbonyl-4-piperidinyl)-methyl]amine;[1-(tert-butoxycarbonyl)piperidin-4-yl]methylamine;1-(tert-butyloxycarbonyl)-4-(aminomethyl)piperidine;Q-102979;tert-butyl-4-(aminomethyl)-piperidine-1-carboxylate;tertiary butyl 4-(aminomethyl)piperidine-1-carboxylate;4-(aminomethyl)piperidine-1-carboxylic tert-butyl ester;Z382715692;racemic tert-butyl 4-(aminomethyl)piperidine-1-carboxylate;t-butyl 4-(aminomethyl)tetrahydropyridine-1(2H)-carboxylate;4-(aminomethyl)piperidine-1-carboxylic acid tert-butyl ester;4-(aminomethyl)-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester

Suppliers and Price of 1-Boc-4-(aminomethyl)piperidine

Supply Marketing:Edit

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

TRC
N-Boc-4-(aminomethyl)piperidine
25g
$ 350.00

TCI Chemical
4-(Aminomethyl)-1-tert-butoxycarbonylpiperidine >98.0%(GC)(T)
5g
$ 183.00

TCI Chemical
4-(Aminomethyl)-1-tert-butoxycarbonylpiperidine >98.0%(GC)(T)
1g
$ 73.00

Sigma-Aldrich
1-Boc-4-(aminomethyl)piperidine 97%
5g
$ 47.30

Sigma-Aldrich
1-Boc-4-(aminomethyl)piperidine 97%
25g
$ 217.00

Oakwood
4-(Aminomethyl)-1-N-Boc-piperidine 97%
25g
$ 80.00

Oakwood
4-(Aminomethyl)-1-N-Boc-piperidine 97%
5g
$ 20.00

Oakwood
4-(Aminomethyl)-1-N-Boc-piperidine 97%
1g
$ 10.00

Matrix Scientific
tert-Butyl 4-(aminomethyl)piperidine-1-carboxylate
1g
$ 10.00

Matrix Scientific
tert-Butyl 4-(aminomethyl)piperidine-1-carboxylate
5g
$ 14.00

Total 107 raw suppliers

Chemical Property of 1-Boc-4-(aminomethyl)piperidine Edit

Chemical Property:

Vapor Pressure:0.00325mmHg at 25°C
Refractive Index:n20/D 1.473(lit.)
Boiling Point:299.4 °C at 760 mmHg
PKA:10.13±0.29(Predicted)
Flash Point:134.9 °C
PSA：55.56000
Density:1.023 g/cm³
LogP:2.23040
Storage Temp.:Room temperature.
Solubility.:Soluble in chloroform and methanol.
XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:214.168127949
Heavy Atom Count:15
Complexity:215

Purity/Quality:

99.9% ^*data from raw suppliers

N-Boc-4-(aminomethyl)piperidine ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi,C
Hazard Codes:Xi,C,N
Statements: 36/37/38-34-50
Safety Statements: 26-36-45-36/37/39-24/25-23-61

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CC(C)(C)OC(=O)N1CCC(CC1)CN
Uses 1-Boc-4-(aminomethyl)piperidine is a protected 4-substituted piperidinecarboxylate used in the preparation of orally active platelet-activating factor antagonists as well as other biologically active compounds. 4-Aminomethyl-1-Boc-piperidine is used in the preparation biologically active compounds and orally active platelet-activating factor antagonists. It is used as an inhibitor for aspartic acid protease and Kinesin spindle protein. It is an active reactant involved in the enantioselective synthesis of N-alkyl terminal aziridines.

Technology Process of 1-Boc-4-(aminomethyl)piperidine

There total 32 articles about 1-Boc-4-(aminomethyl)piperidine 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: 100.0%