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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)-

N-[3-(1H-benzimidazol-2-yl)-4-chlorophenyl]-3,4,5-triethoxybenzamide

CCOc1c(OCC)cc(cc1OCC)C(=O)Nc1ccc(c(c1)c1nc2c([nH]1)cccc2)Cl Request for Quotation
Chemical Name: N-[3-(1H-benzimidazol-2-yl)-4-chlorophenyl]-3,4,5-triethoxybenzamide
CAS Number: 329196-48-7
Product Number: AG00CHLN(AGN-PC-0K4AVW)
Synonyms:
MDL No:
Molecular Formula: C26H26ClN3O4
Molecular Weight: 479.9553

Identification/Properties

Properties
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
479.961g/mol
XLogP3:
5.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
9
Exact Mass:
479.161g/mol
Monoisotopic Mass:
479.161g/mol
Topological Polar Surface Area:
85.5A^2
Heavy Atom Count:
34
Formal Charge:
0
Complexity:
640
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


SANT-2, a highly versatile organosilane compound, plays a crucial role in various chemical synthesis applications. Due to its unique properties, SANT-2 is widely utilized as a coupling agent in organic reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its ability to facilitate cross-coupling reactions makes it an invaluable tool in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, SANT-2 is employed as a key reagent in the functionalization of substrates, enabling the introduction of specific functional groups with high efficiency and selectivity. The versatility and reactivity of SANT-2 make it a valuable asset in the toolkit of synthetic chemists aiming to achieve complex molecular transformations with precision and reliability.