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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

tert-butyl N-[(3R)-1-piperidin-4-ylpyrrolidin-3-yl]carbamate

O=C(OC(C)(C)C)NC1CCN(C1)C1CCNCC1 Request for Quotation
Chemical Name: tert-butyl N-[(3R)-1-piperidin-4-ylpyrrolidin-3-yl]carbamate
CAS Number: 903094-57-5
Product Number: AG00GRVX(AGN-PC-05IZFI)
Synonyms:
MDL No:
Molecular Formula: C14H27N3O2
Molecular Weight: 269.3831

Identification/Properties

Computed Properties
Molecular Weight:
269.389g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
269.21g/mol
Monoisotopic Mass:
269.21g/mol
Topological Polar Surface Area:
53.6A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
308
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl (1-(piperidin-4-yl)pyrrolidin-3-yl)carbamate is a versatile compound widely utilized in chemical synthesis processes. With its unique structure, this compound serves as a valuable building block in the creation of various organic molecules. By strategically incorporating this carbamate derivative into synthetic pathways, researchers can introduce specific functional groups and stereochemistry into their target molecules with precision. This compound's compatibility with a range of synthetic methodologies makes it an essential tool for synthesizing complex organic structures efficiently and effectively. From pharmaceuticals to materials science, the application of tert-Butyl (1-(piperidin-4-yl)pyrrolidin-3-yl)carbamate in chemical synthesis offers endless possibilities for innovation and discovery.