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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)-

Butanamide, N-(2-hydroxyethyl)-3-oxo-

OCCNC(=O)CC(=O)C Request for Quotation
Chemical Name: Butanamide, N-(2-hydroxyethyl)-3-oxo-
CAS Number: 24309-97-5
Product Number: AG006WKI(AGN-PC-0JLYNZ)
Synonyms:
MDL No:
Molecular Formula: C6H11NO3
Molecular Weight: 145.1564

Identification/Properties

Properties
MP:
104-106℃
BP:
373.7°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
145.158g/mol
XLogP3:
-1.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
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:
133
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(2-Hydroxyethyl)-3-oxobutanamide, also known as $name$, is a critical compound used in chemical synthesis. This compound serves as a versatile building block in organic chemistry reactions, primarily functioning as a key intermediate in the synthesis of various organic molecules. $name$ plays a crucial role in forming complex structures and functional groups due to its unique chemical properties.In chemical synthesis, this compound is widely employed for its ability to participate in condensation reactions, allowing for the formation of carbon-carbon and carbon-nitrogen bonds. The presence of the hydroxyethyl group enhances reactivity, enabling $name$ to act as a nucleophile or electrophile in different reaction pathways. This versatility makes it highly valuable in the production of pharmaceuticals, agrochemicals, and advanced materials.Additionally, N-(2-Hydroxyethyl)-3-oxobutanamide can be utilized as a protecting group in organic synthesis to temporary shield sensitive functional groups and prevent unwanted side reactions. Through selective deprotection, the desired chemical transformations can be achieved, leading to the successful synthesis of intricate organic molecules.With its diverse applications and crucial role in chemical synthesis, $name$ stands as a fundamental component in the development of new compounds and materials in the field of organic chemistry.