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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)-

3-Pyridinecarboxamide, 2-chloro-4-methyl-

NC(=O)c1c(C)ccnc1Cl Request for Quotation
Chemical Name: 3-Pyridinecarboxamide, 2-chloro-4-methyl-
CAS Number: 152362-01-1
Product Number: AG003GXH(AGN-PC-0ND8EW)
Synonyms:
MDL No: MFCD09033826
Molecular Formula: C7H7ClN2O
Molecular Weight: 170.5963

Identification/Properties

Properties
MP:
181.3° - 182.0°C
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
170.596g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
170.025g/mol
Monoisotopic Mass:
170.025g/mol
Topological Polar Surface Area:
56A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
163
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


2-Chloro-4-methylnicotinamide is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. As a key building block in organic chemistry, this compound serves as a crucial intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its incorporation in the synthesis of complex molecules allows for the introduction of specific functional groups, facilitating the creation of novel compounds with enhanced biological activities or improved physical properties. Furthermore, 2-Chloro-4-methylnicotinamide can participate in a variety of reactions such as nucleophilic substitutions, condensations, and metal-catalyzed transformations, offering a broad spectrum of synthetic pathways for the preparation of diverse chemical entities. By strategically utilizing this compound in chemical synthesis, researchers and chemists can access new avenues for developing innovative products and advancing scientific discoveries.