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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-Boc-amino-tetrahydropyran-4-yl)acetic acid

O=C(NC1(CCOCC1)CC(=O)O)OC(C)(C)C Request for Quotation
Chemical Name: (4-Boc-amino-tetrahydropyran-4-yl)acetic acid
CAS Number: 946682-30-0
Product Number: AG00IIFK(AGN-PC-0WAHSZ)
Synonyms:
MDL No:
Molecular Formula: C12H21NO5
Molecular Weight: 259.2988

Identification/Properties

Computed Properties
Molecular Weight:
259.302g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
5
Exact Mass:
259.142g/mol
Monoisotopic Mass:
259.142g/mol
Topological Polar Surface Area:
84.9A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
315
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:
H302-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-Boc-amino-tetrahydropyran-4-yl)acetic acid is a versatile compound widely utilized in chemical synthesis processes, particularly in peptide synthesis and medicinal chemistry. Its unique structure and reactivity make it an essential building block for the preparation of various pharmaceuticals, peptides, and other organic molecules.This compound serves as a key intermediate for the modification and functionalization of peptides due to its ability to protect the amine group with the Boc (tert-butoxycarbonyl) protecting group. By incorporating (4-Boc-amino-tetrahydropyran-4-yl)acetic acid into peptide sequences, chemists can control the reactivity and selectivity of amino acid residues during peptide assembly, thus enabling the synthesis of complex peptide structures with high purity and yield.Additionally, the (4-Boc-amino-tetrahydropyran-4-yl)acetic acid can be used for the synthesis of peptidomimetics, heterocycles, and other bioactive compounds through various chemical transformations such as amidation, esterification, and coupling reactions. Its compatibility with standard peptide synthesis protocols and its stability under a wide range of reaction conditions make it a valuable tool for organic chemists seeking to access diverse molecular scaffolds for drug discovery and development.Overall, the (4-Boc-amino-tetrahydropyran-4-yl)acetic acid plays a crucial role in modern organic synthesis by enabling the efficient and selective construction of complex peptide-based molecules with potential applications in medicine, biochemistry, and materials science.