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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-[[(2-methylpropan-2-yl)oxycarbonylamino]methyl]oxane-4-carboxylic acid

O=C(OC(C)(C)C)NCC1(CCOCC1)C(=O)O Request for Quotation
Chemical Name: 4-[[(2-methylpropan-2-yl)oxycarbonylamino]methyl]oxane-4-carboxylic acid
CAS Number: 946761-11-1
Product Number: AG00IIG1(AGN-PC-01A9TS)
Synonyms:
MDL No:
Molecular Formula: C12H21NO5
Molecular Weight: 259.2988

Identification/Properties

Computed Properties
Molecular Weight:
259.302g/mol
XLogP3:
0.6
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#:
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


4-(((tert-Butoxycarbonyl)amino)methyl)tetrahydro-2H-pyran-4-carboxylic acid is a versatile compound commonly used in chemical synthesis for its unique properties in building more complex molecules. This compound serves as a key building block in the synthesis of various pharmaceuticals, organic compounds, and specialty chemicals due to its ability to undergo selective reactions and introduce specific functional groups. Its primary application lies in the formation of peptide bonds, making it a valuable tool in peptide synthesis methodologies. Additionally, its tetrahydro-2H-pyran ring structure provides stability and rigidity to the molecules it is incorporated into, enhancing their overall chemical and biological properties. This compound plays a crucial role in the development of novel compounds with potential applications in drug discovery, materials science, and other fields requiring precise chemical design.