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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 4-(pyrrolidin-3-yl)piperidine-1-carboxylate

O=C(N1CCC(CC1)C1CNCC1)OC(C)(C)C Request for Quotation
Chemical Name: tert-Butyl 4-(pyrrolidin-3-yl)piperidine-1-carboxylate
CAS Number: 1314771-79-3
Product Number: AG00HSHD(AGN-PC-0WQY16)
Synonyms:
MDL No: MFCD19700141
Molecular Formula: C14H26N2O2
Molecular Weight: 254.3684

Identification/Properties

Computed Properties
Molecular Weight:
254.374g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
254.199g/mol
Monoisotopic Mass:
254.199g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
291
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 4-(pyrrolidin-3-yl)piperidine-1-carboxylate is a versatile compound widely used in chemical synthesis due to its unique structure and reactivity. This compound serves as an essential building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its incorporation in organic synthesis enables the efficient production of complex molecules with specific structural properties, making it a valuable tool for medicinal chemists and research scientists. In particular, tert-Butyl 4-(pyrrolidin-3-yl)piperidine-1-carboxylate plays a crucial role in the development of drug candidates with potential therapeutic benefits by serving as a key intermediate in the synthesis of bioactive compounds. Additionally, this compound's utility extends to the creation of advanced materials, dyes, and functional polymers, highlighting its significance in the field of chemical synthesis.