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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)-

3-AMINOMETHYL-1-N-FMOC-PIPERIDINE HYDROCHLORIDE

NCC1CCCN(C1)C(=O)OCC1c2ccccc2c2c1cccc2.Cl Request for Quotation
Chemical Name: 3-AMINOMETHYL-1-N-FMOC-PIPERIDINE HYDROCHLORIDE
CAS Number: 669713-56-8
Product Number: AG00FAY1(AGN-PC-0KKL3G)
Synonyms:
MDL No:
Molecular Formula: C21H25ClN2O2
Molecular Weight: 372.8884

Identification/Properties

Computed Properties
Molecular Weight:
372.893g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
372.16g/mol
Monoisotopic Mass:
372.16g/mol
Topological Polar Surface Area:
55.6A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
447
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Fmoc-3-Aminomethylpiperidine hydrochloride is a key compound utilized in chemical synthesis as a versatile building block for the fabrication of complex organic molecules. This compound serves as a crucial intermediate for the synthesis of peptides, peptidomimetics, and other bioactive compounds. By incorporating the 1-Fmoc-3-Aminomethylpiperidine hydrochloride into various chemical reactions, chemists can efficiently modify and functionalize molecules to create novel structures with tailored properties. Its unique structure and reactivity make it an indispensable tool in the field of organic chemistry, enabling the creation of diverse molecular architectures for pharmaceutical, material science, and other research applications.