1. Home
  2. Acetic acid, [(1-methylethyl)amino]oxo-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Acetic acid, [(1-methylethyl)amino]oxo-

CC(NC(=O)C(=O)O)C Request for Quotation
Chemical Name: Acetic acid, [(1-methylethyl)amino]oxo-
CAS Number: 29262-57-5
Product Number: AG002XVT(AGN-PC-0LXBTW)
Synonyms:
MDL No: MFCD06740186
Molecular Formula: C5H9NO3
Molecular Weight: 131.1299

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
131.131g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
131.058g/mol
Monoisotopic Mass:
131.058g/mol
Topological Polar Surface Area:
66.4A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
130
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

Request for Quotation

Customer Feedback

Chemical Structure


2-(Isopropylamino)-2-oxoacetic acid, also known as IPA-oxoacetic acid, is a versatile compound commonly used in chemical synthesis. This specific molecule plays a crucial role as a building block in the creation of various pharmaceuticals, agrochemicals, and other specialty chemicals. By introducing this compound into a synthesis pathway, chemists can manipulate its structure and properties to design and produce a wide range of complex molecules with desired functions.In chemical synthesis, 2-(Isopropylamino)-2-oxoacetic acid serves as a key intermediate for the preparation of diverse compounds due to its unique structural features. Its functional groups and reactivity enable the formation of new carbon-carbon and carbon-nitrogen bonds, facilitating the construction of multi-functional molecules in a sequential manner. This compound acts as a valuable starting material for the synthesis of drug candidates, bioactive compounds, and advanced materials by serving as a foundation for further bond formations and modifications.Moreover, the presence of the isopropylamino group in 2-(Isopropylamino)-2-oxoacetic acid imparts distinct chemical properties that can be leveraged in synthetic strategies. The isopropylamino moiety not only serves as a directing group for selective reactions but also influences the overall reactivity and stereochemistry of the intermediate and final products. This enables chemists to tailor the synthesis process to achieve specific molecular structures and properties required for targeted applications in pharmaceutical research, materials science, and agricultural chemistry.Overall, the strategic use of 2-(Isopropylamino)-2-oxoacetic acid in chemical synthesis offers a versatile and efficient approach to access a diverse array of functionalized molecules with applications across various industries. Its role as a building block in synthetic pathways highlights its significance in advancing the development of novel compounds with potential therapeutic, agricultural, or technological benefits.