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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)-

ethyl 3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate

CCOC(=O)CCNC(=O)OC(C)(C)C Request for Quotation
Chemical Name: ethyl 3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate
CAS Number: 88574-53-2
Product Number: AG00IF7P(AGN-PC-00Q36G)
Synonyms:
MDL No: MFCD10000637
Molecular Formula: C10H19NO4
Molecular Weight: 217.2622

Identification/Properties

Computed Properties
Molecular Weight:
217.265g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
217.131g/mol
Monoisotopic Mass:
217.131g/mol
Topological Polar Surface Area:
64.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
220
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 3-[(tert-butoxy)carbonyl]amino)propanoate is a valuable compound widely utilized in chemical synthesis due to its utility as a versatile building block. This compound is particularly useful in peptide chemistry and organic synthesis processes involving amino acid derivatives. By serving as a key intermediate, it facilitates the efficient creation of complex molecules with specific structures and properties. Additionally, Ethyl 3-[(tert-butoxy)carbonyl]amino)propanoate enables chemists to carry out selective transformations and functional group manipulations, enhancing the overall synthetic strategy. Its compatibility with various reaction conditions and compatibility with a range of reagents make it an indispensable tool for chemists working in the field of organic chemistry and drug development.