Home Carboxys tert-butyl piperidine-1-carboxylate

tert-butyl piperidine-1-carboxylate

CAS No.:
75844-69-8
Catalog Number:
AG0038G3
Molecular Formula:
C10H19NO2
Molecular Weight:
185.2634
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$13
- +
25g
95%
In Stock USA
United States
$38
- +
100g
95%
In Stock USA
United States
$119
- +
500g
95%
In Stock USA
United States
$475
- +
Product Description
Catalog Number:
AG0038G3
Chemical Name:
tert-butyl piperidine-1-carboxylate
CAS Number:
75844-69-8
Molecular Formula:
C10H19NO2
Molecular Weight:
185.2634
MDL Number:
MFCD02093935
IUPAC Name:
tert-butyl piperidine-1-carboxylate
InChI:
InChI=1S/C10H19NO2/c1-10(2,3)13-9(12)11-7-5-4-6-8-11/h4-8H2,1-3H3
InChI Key:
RQCNHUCCQJMSRG-UHFFFAOYSA-N
SMILES:
O=C(N1CCCCC1)OC(C)(C)C
EC Number:
616-270-3
Properties
Complexity:
178  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
185.142g/mol
Formal Charge:
0
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
185.267g/mol
Monoisotopic Mass:
185.142g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
29.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2  
Literature
Title Journal
Dynamics of catalytic resolution of 2-lithio-N-Boc-piperidine by ligand exchange. Journal of the American Chemical Society 20121010
Regioselective and stereoselective copper(I)-promoted allylation and conjugate addition of N-Boc-2-lithiopyrrolidine and N-Boc-2-lithiopiperidine. The Journal of organic chemistry 20100618
Asymmetric deprotonation of N-boc piperidine: react IR monitoring and mechanistic aspects. Journal of the American Chemical Society 20100602
Asymmetric substitutions of 2-lithiated N-boc-piperidine and N-Boc-azepine by dynamic resolution. Chemistry (Weinheim an der Bergstrasse, Germany) 20100406
Synthesis of 2-arylpiperidines by palladium couplings of aryl bromides with organozinc species derived from deprotonation of N-boc-piperidine. Organic letters 20080904
Dynamic kinetic and kinetic resolution of N-Boc-2-lithiopiperidine. Chemical communications (Cambridge, England) 20071121
An experimental and theoretical study of the asymmetric lithiation of 1,2,3,5,6,7-hexahydro-3a,4a-diazacyclopenta[def]phenanthren-4-one. The Journal of organic chemistry 20070202
Reactivity series for s-BuLi/diamine-mediated lithiation of N-Boc pyrrolidine: applications in catalysis and lithiation of N-Boc piperidine. Chemical communications (Cambridge, England) 20060628
Synthesis of methylphenidate analogues and their binding affinities at dopamine and serotonin transport sites. Bioorganic & medicinal chemistry letters 20040405
An experimental and computational investigation of the enantioselective deprotonation of Boc-piperidine. Journal of the American Chemical Society 20020306
Properties