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N-Boc-piperidine_Molecular_structure_CAS_75844-69-8)
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N-Boc-piperidine

Catalog No. 655872 Name Sigma Aldrich
CAS Number 75844-69-8 Website http://www.sigmaaldrich.com
M. F. C10H19NO2 Telephone 1-800-521-8956
M. W. 185.26336 Fax
Purity 98% Email
Storage Chembase ID: 17963

SYNONYMS

Title
N-Boc-哌啶
IUPAC name
tert-butyl piperidine-1-carboxylate
IUPAC Traditional name
tert-butyl piperidine-1-carboxylate
Synonyms
1-Boc-哌啶
N-Boc-tetrahydropyridine
N-叔丁氧羰基哌啶
1-Boc-piperidine
N-(tert-Butoxycarbonyl)piperidine

DATABASE IDS

MDL Number MFCD02093935
CAS Number 75844-69-8
PubChem SID 24884129

PROPERTIES

Empirical Formula (Hill Notation) C10H19NO2
Purity 98%
Density 0.964 g/mL at 25 °C(lit.)
Flash Point 86 °C
Flash Point 186.8 °F
Refractive Index n20/D 1.454(lit.)
GHS Pictograms GHS06
GHS Pictograms GHS09
GHS Signal Word Danger
GHS Hazard statements H301-H315-H319-H335-H400
European Hazard Symbols Toxic Toxic (T)
European Hazard Symbols Nature polluting Nature polluting (N)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P261-P273-P301 + P310-P305 + P351 + P338
RID/ADR UN 2810 6.1/PG 3
Risk Statements 25-36/37/38-50
Safety Statements 26-36-45-60-61
Hazard Class 6.1
UN Number 2810
Packing Group 3
German water hazard class 3

DETAILS

Description (English)
Application
Substrate used in a two-step α-arylation procedure.7
Reactant for synthesis of:
• Piperazine derivatives for orally active acetyl-CoA carboxylase 1/2 non-selective inhibitors1
• 2-Aryl and 2-vinyl piperidines2
• Allosteric IGF-1R inhibitors3Reactant for:
• Allylation and conjugate addition reactions4
• Asymmetric deprotonation5
• Enantioselective inter- and intramolecular aldol reactions6
Packaging
5, 25 g in glass bottle
Description (简体中文)
Application
用作两步法 α-芳基化过程的底物。7
Reactant for synthesis of:
• Piperazine derivatives for orally active acetyl-CoA carboxylase 1/2 non-selective inhibitors1
• 2-Aryl and 2-vinyl piperidines2
• Allosteric IGF-1R inhibitors3Reactant for:
• Allylation and conjugate addition reactions4
• Asymmetric deprotonation5
• Enantioselective inter- and intramolecular aldol reactions6
包装
5, 25 g in glass bottle

REFERENCES