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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)-

6,7-dimethyl-3-[[methyl-[2-[methyl-[[1-[3-(trifluoromethyl)phenyl]indol-3-yl]methyl]amino]ethyl]amino]methyl]chromen-4-one

CN(Cc1cn(c2c1cccc2)c1cccc(c1)C(F)(F)F)CCN(Cc1coc2c(c1=O)cc(c(c2)C)C)C Request for Quotation
Chemical Name: 6,7-dimethyl-3-[[methyl-[2-[methyl-[[1-[3-(trifluoromethyl)phenyl]indol-3-yl]methyl]amino]ethyl]amino]methyl]chromen-4-one
CAS Number: 869998-49-2
Product Number: AG00GTBQ(AGN-PC-0LQ2MS)
Synonyms:
MDL No:
Molecular Formula: C32H32F3N3O2
Molecular Weight: 547.6106

Identification/Properties

Computed Properties
Molecular Weight:
547.622g/mol
XLogP3:
6.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
8
Exact Mass:
547.245g/mol
Monoisotopic Mass:
547.245g/mol
Topological Polar Surface Area:
37.7A^2
Heavy Atom Count:
40
Formal Charge:
0
Complexity:
910
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


SPD 304, also known as a silicone-based catalyst, is a versatile tool in chemical synthesis due to its high thermal stability and excellent catalytic properties. This catalyst is particularly sought after in the production of polymers, where it facilitates the polymerization process and enhances the quality of the final product. Additionally, SPD 304 is widely used in the synthesis of specialty chemicals, such as pharmaceutical intermediates and fine chemicals, where precise control over reaction conditions is crucial for obtaining desired yields and purity levels. In organic synthesis, SPD 304 serves as a reliable catalyst for a variety of reactions, including cross-coupling reactions, hydrogenation, and hydrosilylation. Its compatibility with a wide range of functional groups and substrates makes it a popular choice among chemists seeking efficient and selective catalytic solutions. By leveraging the unique properties of SPD 304, chemists can accelerate reaction rates, improve product yields, and streamline synthetic routes in diverse chemical applications.