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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)-

(4-Fmoc-amino-1-Boc-piperidin-4-yl)acetic acid

OC(=O)CC1(CCN(CC1)C(=O)OC(C)(C)C)NC(=O)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: (4-Fmoc-amino-1-Boc-piperidin-4-yl)acetic acid
CAS Number: 946682-26-4
Product Number: AG00IIFJ(AGN-PC-0WBO6I)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
480.561g/mol
XLogP3:
4.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
8
Exact Mass:
480.226g/mol
Monoisotopic Mass:
480.226g/mol
Topological Polar Surface Area:
105A^2
Heavy Atom Count:
35
Formal Charge:
0
Complexity:
763
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (4-Fmoc-amino-1-Boc-piperidin-4-yl)acetic acid is a versatile compound commonly used in chemical synthesis due to its unique properties. This compound serves as a key building block in peptide and organic synthesis processes. With its Fmoc-protected amino group and Boc-protected piperidine ring, this acid derivative acts as an essential intermediate in the formation of complex peptides and organic molecules.In chemical synthesis, (4-Fmoc-amino-1-Boc-piperidin-4-yl)acetic acid plays a crucial role in the creation of peptide bonds through peptide coupling reactions. Its Fmoc-protected amino group allows for selective deprotection and coupling with other amino acids, enabling the stepwise assembly of peptide chains. Additionally, the Boc-protected piperidine ring provides stability and protection to the intermediate compounds during the synthesis process.Moreover, this compound can be utilized in the preparation of drug molecules, bioconjugates, and other biologically active compounds. Its compatibility with standard peptide synthesis protocols and its versatility make it an indispensable tool for chemists working in the fields of medicinal chemistry, drug discovery, and bioorganic chemistry. The (4-Fmoc-amino-1-Boc-piperidin-4-yl)acetic acid is a valuable building block that enables the efficient and precise synthesis of complex organic molecules with diverse applications.