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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)-

Propanamide, N-(3-formyl-4-pyridinyl)-2,2-dimethyl-

O=Cc1cnccc1NC(=O)C(C)(C)C Request for Quotation
Chemical Name: Propanamide, N-(3-formyl-4-pyridinyl)-2,2-dimethyl-
CAS Number: 86847-71-4
Product Number: AG004IQ8(AGN-PC-0KKZQB)
Synonyms:
MDL No:
Molecular Formula: C11H14N2O2
Molecular Weight: 206.2411

Identification/Properties

Properties
Storage:
2-8℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
206.245g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
206.106g/mol
Monoisotopic Mass:
206.106g/mol
Topological Polar Surface Area:
59.1A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
246
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:
H317-H319
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-(3-Formylpyridin-4-yl)pivalamide is a versatile compound widely used in chemical synthesis as a key building block for the preparation of various organic molecules. It serves as an important intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.In organic chemistry, N-(3-Formylpyridin-4-yl)pivalamide is commonly employed as a starting material for the construction of heterocyclic compounds, which are essential in drug discovery and development. Its unique structure containing a formyl group and a pyridine ring allows for diverse functionalization reactions, enabling the introduction of different substituents to modulate the properties of the final product.Furthermore, the pivalamide moiety in N-(3-Formylpyridin-4-yl)pivalamide provides steric hindrance and stability, making it an ideal protecting group for sensitive functional groups during chemical transformations. This protection-deprotection strategy facilitates selective reactions and improves overall yields in complex synthesis routes.Overall, N-(3-Formylpyridin-4-yl)pivalamide plays a crucial role in the assembly of complex organic molecules with tailored properties, making it a valuable tool for chemists in the field of chemical synthesis.