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1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde

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1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde Basic information

Product Name:
1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde
Synonyms:
  • 1-(tert-butoxycarbonyl)-4-formylpiperidine
  • 1-BOC-4-FORMYLPIPERIDINE 95%
  • 1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde
  • Piperidine-4-carboxaldehyde, N-BOC protected
  • TERT-BUTYL 4-FORMYLPIPERIDINE-1-CARBOXYLATE
  • 1-Piperidinecarboxylic acid, 4-formyl-, 1,1-dimethylethyl ester
  • 1-TERT-BUTOXYCARBONYLPIPERIDINE-4-CARBOXALDEHYDE
  • tert-Butyl 4-formyl-1-piperidinecarboxylate
CAS:
137076-22-3
MF:
C11H19NO3
MW:
213.27
EINECS:
203-107-6
Product Categories:
  • C11
  • Chemical Synthesis
  • Piperidine
  • Heterocyclic Building Blocks
  • Organic Building Blocks
  • Piperidines
  • Carbonyl Compounds
  • Heterocycles
  • pharmacetical
  • Aldehydes
  • Pyrans, Piperidines & Piperazines
  • Inhibitors
  • Building Blocks
  • C10-C12
Mol File:
137076-22-3.mol
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1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde Chemical Properties

Melting point:
34-40℃
Boiling point:
295.4±33.0 °C(Predicted)
Density 
1.114±0.06 g/cm3(Predicted)
Flash point:
>110℃
storage temp. 
2-8°C
solubility 
Soluble in methanol.
pka
-2.13±0.40(Predicted)
form 
Oil
color 
Clear Yellow
Sensitive 
Air Sensitive
InChIKey
JYUQEWCJWDGCRX-UHFFFAOYSA-N
CAS DataBase Reference
137076-22-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,N,Xn
Risk Statements 
36/37/38-50-22
Safety Statements 
26-36/37/39-61
RIDADR 
UN 3077 9/PG 3
HS Code 
29333990
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1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde Usage And Synthesis

Chemical Properties

Clear Yellow Oil

Uses

Reactant for synthesis of:• ;Pim-1 inhibitors1• ;Selective GPR119 agonists for type II diabetes2• ;M-tropic (R5) HIV-1 replication inhibitors3• ;HDAC inhibitors4• ;Selective 5-HT6 antagonists5Reactant for three-component vinylogous Mannich reactions6

Uses

1-Boc-piperidine-4-carboxaldehyde is used as reactant for synthesis of Pim-1 inhibitors, selective GPR119 agonists for type II diabetes, M-tropic (R5) HIV-1 replication inhibitors, HDAC inhibitors and selective 5-HT6 antagonists. It is also used as reactant for three-component vinylogous Mannich reactions

Uses

An intermediate for polycyclic indazole derivatives that are ERK inhibitors.

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