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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)-

Glycine, N-[(1,1-dimethylethoxy)carbonyl]-N-ethyl-

CCN(C(=O)OC(C)(C)C)CC(=O)O Request for Quotation
Chemical Name: Glycine, N-[(1,1-dimethylethoxy)carbonyl]-N-ethyl-
CAS Number: 149794-10-5
Product Number: AG0038XF(AGN-PC-00KCXR)
Synonyms:
MDL No:
Molecular Formula: C9H17NO4
Molecular Weight: 203.2356

Identification/Properties

Computed Properties
Molecular Weight:
203.238g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
203.116g/mol
Monoisotopic Mass:
203.116g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
219
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


The application of Boc-N-Ethylglycine in chemical synthesis lies in its utility as a versatile building block for the modification of various molecules. This compound, possessing a tert-butoxycarbonyl (Boc) protected amino group and an ethylglycine moiety, serves as a valuable intermediate in the creation of complex organic compounds. With its ability to undergo selective deprotection and further functionalization, Boc-N-Ethylglycine contributes significantly to the synthesis of peptides, pharmaceuticals, and other bioactive molecules. In peptide chemistry, it is commonly employed to introduce specific sequences or structural motifs, paving the way for the development of novel therapeutic agents and probes. Additionally, its compatibility with various chemical reactions and purification techniques makes it a favored tool in both academic research and industrial settings. Overall, the strategic incorporation of Boc-N-Ethylglycine enables chemists to access a wide array of tailored compounds with enhanced properties and diverse applications in the field of organic chemistry.