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641472

Sigma-Aldrich

1-Boc-4-(aminomethyl)piperidine

97%

Synonym(s):

1,1-Dimethylethyl 4-(aminomethyl)-1-piperidinecarboxylate, N-(tert-Butoxycarbonyl)-4-aminomethylpiperidine

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About This Item

Empirical Formula (Hill Notation):
C11H22N2O2
CAS Number:
144222-22-0
Molecular Weight:
214.30
MDL number:
MFCD01076207
UNSPSC Code:
12352100
PubChem Substance ID:
24883120
NACRES:
NA.22

assay

97%

refractive index

n20/D 1.473 (lit.)

bp

237-238 °C (lit.)

density

1.013 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

CC(C)(C)OC(=O)N1CCC(CN)CC1

InChI

1S/C11H22N2O2/c1-11(2,3)15-10(14)13-6-4-9(8-12)5-7-13/h9H,4-8,12H2,1-3H3

Inchi Key

KLKBCNDBOVRQIJ-UHFFFAOYSA-N

Related Categories

Application

Precursor in the preparation of a variety of different protein agonists or antagonists including:
  • Kinesin spindle protein inhibitors with potential anticancer activity
  • Orphan G-protein coupled receptor GPR119 agonist with antidiabetic potential
  • Pim-1 inhibitors
  • Aspartic acid protease inhibitors

Reactant involved in enantioselective synthesis of N-alkyl terminal aziridines

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

No data available

flash_point_c

No data available

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCM7530
MKCF5363
MKBW3363V
MKBN5512V
MKBF4044

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Articles

MRT - Mono-Boc-Protection of Diamines

Mono-Boc-protected diamines are versatile building blocks for chemical synthesis. Their production is a lot more challenging than the simple reaction scheme might imply, because the Boc-anhydride reagent cannot differentiate between the two identical amino moieties in the substrate.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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