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Merck
CN

713724

Ethyl N-Boc-piperidine-3-carboxylate

≥97.0%

Synonym(s):

1-(tert-Butoxycarbonyl)-piperidine-3-carboxylic acid ethyl ester, 1-(tert-Butyl) 3-ethyl 1,3-piperidinedicarboxylate, N-Boc-DL-nipecotic acid ethyl ester, Ethyl N-Boc-DL-nipecotate

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About This Item

Empirical Formula (Hill Notation):
C13H23NO4
CAS Number:
130250-54-3
Molecular Weight:
257.33
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
329763214
MDL number:
MFCD04116274
Beilstein/REAXYS Number:
3614917

Key Documents

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InChI

1S/C13H23NO4/c1-5-17-11(15)10-7-6-8-14(9-10)12(16)18-13(2,3)4/h10H,5-9H2,1-4H3

SMILES string

CCOC(=O)C1CCCN(C1)C(=O)OC(C)(C)C

InChI key

YCXCRFGBFZTUSU-UHFFFAOYSA-N

assay

≥97.0% (GC), ≥97.0%

form

powder

Application

Reactant for synthesis of:
  • GABAA receptor agonists
  • Piperidine derivatives
  • Selective TACE inhibitors
  • HDL-elevating agents
  • α-Sulfonyl hydroxamic acid derivatives
  • chemicals in the Iboga-alkaloid family

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BGBC5292V
1447817V
1452430
1447817

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Synthesis of a Novel Heterospirocyclic 3-(N-Methyl-N-phenylamino)-2H-azirine and its use as an Amino Acid Equivalent in the Preparation of a Model Tripeptide
Villalgordo, J.M. and Heimgartner, M.
Tetrahedron Asymmetry, 49 (33), 7215-7222 (1993)

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