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tert-Butyl piperidine-1-carboxylate
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tert-Butyl piperidine-1-carboxylate

CAS: 75844-69-8

Ref. 3D-FB142536

5gDiscontinued
10gDiscontinued
25gDiscontinued
50gDiscontinued
100gDiscontinued

Discontinued product. For inquiries about similar products, please fill out our form or email us at .


Product Information

Name:
tert-Butyl piperidine-1-carboxylate
Synonyms:
  • 1,1-Dimethylethyl 1-piperidinecarboxylate
  • 1-(tert-Butoxycarbonyl)piperidine
  • 1-Piperidinecarboxylic acid, 1,1-dimethylethyl ester
  • Boc-piperidine
  • N-(tert-Butoxycarbonyl)piperidine
  • Piperidine-1-carboxylic acid tert-butyl ester
  • Tert-Butyl Piperidine-1-Carboxylate
  • tert-Butyl 1-piperidinecarboxylate
Description:

Tert-Butyl piperidine-1-carboxylate (TBPC) is an inhibitor of dopamine β-hydroxylase, an enzyme that catalyzes the conversion of dopamine to norepinephrine. It has been shown to have strong inhibitory properties against trifluoroacetic acid, which is an acidic electrophile. TBPC also has kinetic and thermodynamic properties that are consistent with its role as a proton donor. This compound is synthesized by reacting piperidine with chloroform in the presence of a catalyst such as acetic acid, forming a chiral product. The enantiomeric purity can be controlled by using either racemic or optically pure reactants. Activation energies for the reactions were determined experimentally and are listed in the table below:

The following table lists activation energies for reactions involving TBPC:

Activation Energy (kJ/mol)
Dopamine hydrolysis

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Purity:
Min. 95%
MDL:
Melting point:
Boiling point:
Flash point:
Density:
Concentration:
EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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