(S)-3-Boc-aminopiperidine

Base Information Edit

Chemical Name:(S)-3-Boc-aminopiperidine
CAS No.:216854-23-8
Molecular Formula:C10H20N2O2
Molecular Weight:200.281
Hs Code.:29339900
European Community (EC) Number:626-980-5
DSSTox Substance ID:DTXSID70363795
Wikidata:Q72448377
Mol file:216854-23-8.mol

Synonyms:(S)-3-Boc-aminopiperidine;216854-23-8;(S)-3-N-Boc-aminopiperidine;(S)-tert-butyl piperidin-3-ylcarbamate;tert-butyl N-[(3S)-piperidin-3-yl]carbamate;(S)-3-(Boc-amino)piperidine;(S)-3-(Tert-Butoxycarbonylamino)Piperidine;MFCD03093383;CARBAMIC ACID, (3S)-3-PIPERIDINYL-, 1,1-DIMETHYLETHYL ESTER;TERT-BUTYL (3S)-PIPERIDIN-3-YLCARBAMATE;(S)-3-Bocaminopiperidine;TERT-BUTYL N-[(3S)-3-PIPERIDYL]CARBAMATE;SCHEMBL342108;(s)-3-n-boc-amino piperidine;DTXSID70363795;(S)-BOC-3-AMINOPIPERIDINE;CS-B0850;AKOS005256069;tert-butyl(S)-piperidin-3-ylcarbamate;AC-2190;(5)-tert-butyl piperidin-3-ylcarbamate;(s)-tert-butyl-piperidin-3-ylcarbamate;tert-butyl(3S)-piperidin-3-ylcarbamate;3-(s)-tert-butoxycarbonylaminopiperidine;tert-butyl (s)-piperidin-3-yl-carbamate;(3s)-3-aminopiperidine, 3-boc protected;AS-38496;(S)-3-(tert-butoxycarbonylamino)piperdine;(S)-3-(Boc-amino)piperidine, >=98.0%;AM20090200;B3660;(s)-(-)-3-tert-Butoxycarbonylaminopiperidine;EN300-206041;(3S)-(-)-3-(tert-butoxycarbonylamino)piperidine;(5)-piperidin-3-ylcarbamic acid tert-butyl ester;(s)-piperidin-3-yl-carbamic acid tert-butyl ester;piperidin-3-(S)-yl-carbamic acid tert-butyl ester;Q-103003;Z1203162346

Suppliers and Price of (S)-3-Boc-aminopiperidine

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
(S)-3-(Boc-amino)piperidine
2.5g
$ 1190.00

TRC
(S)-3-(Boc-amino)piperidine
250mg
$ 150.00

TCI Chemical
(S)-3-(tert-Butoxycarbonylamino)piperidine >98.0%(GC)
1g
$ 31.00

TCI Chemical
(S)-3-(tert-Butoxycarbonylamino)piperidine >98.0%(GC)
5g
$ 102.00

Sigma-Aldrich
(S)-3-(Boc-amino)piperidine ≥98.0%
1 g
$ 85.10

Sigma-Aldrich
(S)-3-(Boc-amino)piperidine ≥98.0%
1g-f
$ 85.10

Oakwood
(S)-3-N-Boc-aminopiperidine
1g
$ 10.00

Oakwood
(S)-3-N-Boc-aminopiperidine
5g
$ 25.00

Oakwood
(S)-3-N-Boc-aminopiperidine
25g
$ 80.00

Oakwood
(S)-3-N-Boc-aminopiperidine
100g
$ 210.00

Total 134 raw suppliers

Chemical Property of (S)-3-Boc-aminopiperidine Edit

Chemical Property:

Vapor Pressure:0.000854mmHg at 25°C
Melting Point:122-127 °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.:Room temperature.
Solubility.:Freely soluble in ethanol.
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:

98% ^*data from raw suppliers

(S)-3-(Boc-amino)piperidine ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Statements: 37/38-41-36/37/38
Safety Statements: 26-39-37/39

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NC1CCCNC1
Isomeric SMILES:CC(C)(C)OC(=O)N[C@H]1CCCNC1
Uses (S)-3-N-Boc-aminopiperidine can be useful intermediate for the synthesis of a variety of chiral aminopiperidinyl quinolones as potent antibacterial agents against resistant pathogens; and alkynylpyrimidine amide derivatives as orally a vailable inhibitors of Tie-2 kinase. (S)-3-(Boc-amino)piperidine, is used as an intermediate for pigments. It is also used as important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. It is also an useful intermediate for the synthesis of a variety of chiral aminopiperidinyl quinolones as potent antibacterial agents against resistant pathogens; and alkynylpyrimidine amide derivatives as orally available inhibitors of Tie-2 kinase.

Technology Process of (S)-3-Boc-aminopiperidine

There total 7 articles about (S)-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: 72.0%