3-Boc-aminopiperidine

Base Information

Chemical Name:3-Boc-aminopiperidine
CAS No.:172603-05-3
Molecular Formula:C₁₀H₂₀N₂O₂
Molecular Weight:200.281
Hs Code.:29333990
European Community (EC) Number:676-009-4
DSSTox Substance ID:DTXSID50401088
Nikkaji Number:J2.494.121C
Mol file:172603-05-3.mol

Synonyms:172603-05-3;3-Boc-aminopiperidine;tert-butyl piperidin-3-ylcarbamate;3-N-Boc-aminopiperidine;3-(boc-amino)piperidine;tert-butyl N-(piperidin-3-yl)carbamate;piperidin-3-yl-carbamic acid tert-butyl ester;3-N-Boc-amino piperidine;3-(N-Boc-amino)piperidine;tert-butyl N-piperidin-3-ylcarbamate;tert-butyl n-(3-piperidinyl)carbamate;3-aminopiperidine, 3-boc protected;3-tert-butoxycarbonylaminopiperidine;MFCD03839941;3-(tert-butoxycarbonylamino)piperidine;Piperidin-3-ylcarbamic acid tert-butyl ester;N-3-Piperidinylcarbamic Acid 1,1-Dimethylethyl Ester;MFCD03093382;THALLICACETATE;CARBAMIC ACID, 3-PIPERIDINYL-, 1,1-DIMETHYLETHYL ESTER;R-1-BOC-3-aminopiperdine;3-(N-Boc-amino) piperidine;SCHEMBL219190;t-butyl piperidin-3-ylcarbamate;3-(Boc-amino)piperidine, 97%;t-butyl piperidine-3-ylcarbamate;DTXSID50401088;BCP06666;CS-D0639;tert-butyl piperidin-3-yl-carbamate;tert.butyl piperidin-3-yl-carbamate;3-tert-butyloxycarbonylaminopiperidine;AKOS000169166;AKOS016339690;AC-2177;C-(4-Phenylmorpholin-2-yl)methylamine;EC-0728;PB10276;PB30744;3-tert.-butyloxycarbonylamino-piperidine;TERT-BUTYL 3-PIPERIDINYLCARBAMATE;SY003695;SY005515;SY006326;3-(tert.-butyloxycarbonylamino)-piperidine;Piperidin-3-yl-carbamic acid t-butyl ester;AM20090028;BB 0248299;FT-0601682;FT-0601683;FT-0643653;FT-0650083;FT-0651598;EN300-51971;A13037;A13038;A847289;(RS)-piperidin-3-yl-carbamic acid tert-butyl ester;W-206035;3-piperidinyl-carbamic acid, 1,1-dimethylethyl ester;racemic piperidin-3-yl-carbamic acid tert-butyl ester;F2196-0043;Z285919724;3-(Boc-amino)piperidine

Suppliers and Price of 3-Boc-aminopiperidine

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

TRC
N-3-PiperidinylcarbamicAcid1,1-DimethylethylEster
25g
$ 425.00

Sigma-Aldrich
3-(Boc-amino)piperidine 97%
1g
$ 57.20

Medical Isotopes, Inc.
N-3-PiperidinylcarbamicAcid1,1-DimethylethylEster
100 g
$ 2425.00

Matrix Scientific
tert-Butyl N-(3-piperidinyl)carbamate 95%
5g
$ 38.00

Matrix Scientific
tert-Butyl N-(3-piperidinyl)carbamate 95%
25g
$ 99.00

Labseeker
3-BOC-AMINOPIPERIDINE 98
1g
$ 266.00

Labseeker
3-BOC-AMINOPIPERIDINE 98
2g
$ 306.00

JR MediChem
3-(Boc-Amino)piperidine 97%
100g
$ 798.00

Frontier Specialty Chemicals
3-(Boc-amino)piperidine 98%
1g
$ 70.00

Frontier Specialty Chemicals
3-(Boc-amino)piperidine 98%
5g
$ 230.00

Total 81 raw suppliers

Chemical Property of 3-Boc-aminopiperidine

Chemical Property:

Vapor Pressure:0.000854mmHg at 25°C
Melting Point:102-108°C
Refractive Index:1.479
Boiling Point:304.8 °C at 760 mmHg
PKA:12.37±0.20(Predicted)
Flash Point:138.2 °C
PSA：50.36000
Density:1.02 g/cm³
LogP:1.98280
Storage Temp.:2-8°C
Solubility.:DMSO, Methanol
XLogP3:1.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:200.152477885
Heavy Atom Count:14
Complexity:199

Purity/Quality:

99%, ^*data from raw suppliers

N-3-PiperidinylcarbamicAcid1,1-DimethylethylEster ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi,N
Statements: 36/37/38-50/53
Safety Statements: 26-36/37/39-61-60

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NC1CCCNC1
Uses N-3-Piperidinylcarbamic Acid 1,1-Dimethylethyl Ester is used in the synthesis of highly selective spleen tyrosine kinase inhibitors. Also used in the synthesis of a potent NHE1 inhibitor displaying cardioprotective effects.

Technology Process of 3-Boc-aminopiperidine

There total 46 articles about 3-Boc-aminopiperidine 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: 97.0%