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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-(6-chloro-3-formyl-2-pyridinyl)-2,2-dimethyl-

O=Cc1ccc(nc1NC(=O)C(C)(C)C)Cl Request for Quotation
Chemical Name: Propanamide, N-(6-chloro-3-formyl-2-pyridinyl)-2,2-dimethyl-
CAS Number: 127446-34-8
Product Number: AG000X3J(AGN-PC-002752)
Synonyms:
MDL No:
Molecular Formula: C11H13ClN2O2
Molecular Weight: 240.6861

Identification/Properties

Properties
MP:
137-139℃
BP:
428.644 °C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
240.687g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
240.067g/mol
Monoisotopic Mass:
240.067g/mol
Topological Polar Surface Area:
59.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
276
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:
H315-H317-H319-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(6-Chloro-3-formylpyridin-2-yl)pivalamide is a versatile chemical compound widely utilized in chemical synthesis for its exceptional reactivity and unique structural properties. In synthesis applications, this compound serves as a crucial building block for the preparation of various organic molecules due to its reactive formyl and amino groups, as well as the electron-rich pyridine ring. The presence of the formyl group enables N-(6-Chloro-3-formylpyridin-2-yl)pivalamide to participate in important reactions like nucleophilic addition, condensation, and reduction, allowing chemists to introduce specific functionalities into target molecules. Additionally, the pivalamide moiety serves as a protective group, shielding reactive sites during synthesis and enabling selective transformations.Furthermore, the chloro substituent on the pyridine ring offers opportunities for further derivatization through substitution or coupling reactions, expanding the chemical diversity that can be accessed using this compound. Overall, N-(6-Chloro-3-formylpyridin-2-yl)pivalamide plays a crucial role in the synthesis of complex organic molecules with tailored structures and properties.