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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-(2-methyl-1-oxopropyl)-

CC(C(=O)NCC(=O)O)C Request for Quotation
Chemical Name: Glycine, N-(2-methyl-1-oxopropyl)-
CAS Number: 15926-18-8
Product Number: AG001QKM(AGN-PC-0NBPLD)
Synonyms:
MDL No:
Molecular Formula: C6H11NO3
Molecular Weight: 145.1564

Identification/Properties

Computed Properties
Molecular Weight:
145.158g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
145.074g/mol
Monoisotopic Mass:
145.074g/mol
Topological Polar Surface Area:
66.4A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
142
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


2-Isobutyramidoacetic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis. Its unique chemical structure makes it a valuable reagent in various reactions and processes. In organic synthesis, 2-isobutyramidoacetic acid is commonly employed as a key building block for the preparation of pharmaceutical intermediates, agrochemicals, and specialty chemicals. Its carboxylic acid and amide groups enable it to participate in condensation reactions, esterifications, amidations, and other transformations, leading to the formation of complex molecules with diverse functionalities. The presence of the isobutyryl group also imparts steric and electronic effects, influencing the regioselectivity and stereochemistry of the resulting products. Furthermore, 2-isobutyramidoacetic acid exhibits excellent compatibility with a wide range of solvent systems and reaction conditions, making it a preferred choice for chemists and researchers engaged in the development of novel chemical entities.