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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)-

BenzaMide, 3,4-bis(cyclopropylMethoxy)-N-(3,5-dichloro-4-pyridinyl)-

O=C(c1ccc(c(c1)OCC1CC1)OCC1CC1)Nc1c(Cl)cncc1Cl Request for Quotation
Chemical Name: BenzaMide, 3,4-bis(cyclopropylMethoxy)-N-(3,5-dichloro-4-pyridinyl)-
CAS Number: 1391052-24-6
Product Number: AG001AAC(AGN-PC-0WACHF)
Synonyms:
MDL No:
Molecular Formula: C20H20Cl2N2O3
Molecular Weight: 407.2904

Identification/Properties

Computed Properties
Molecular Weight:
407.291g/mol
XLogP3:
4.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
8
Exact Mass:
406.085g/mol
Monoisotopic Mass:
406.085g/mol
Topological Polar Surface Area:
60.4A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
506
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-H315-H319-H332-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


3,4-Bis(cyclopropylmethoxy)-N-(3,5-dichloropyridin-4-yl)benzamide is a versatile compound widely used in chemical synthesis. Its unique molecular structure makes it a valuable building block for the creation of complex organic molecules. This compound is particularly valuable in the development of novel pharmaceuticals, agrochemicals, and materials due to its reactive functional groups and potential for diverse chemical transformations. In chemical synthesis, 3,4-Bis(cyclopropylmethoxy)-N-(3,5-dichloropyridin-4-yl)benzamide serves as a key intermediate for the introduction of cyclopropylmethoxy and dichloropyridinyl moieties into target molecules. These substituents can impart specific biological activities or material properties, making this compound a crucial component in the construction of advanced organic compounds. Its ability to participate in various chemical reactions, such as coupling reactions, functional group transformations, and heterocyclic synthesis, further highlights its significance in the field of organic chemistry.