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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)-

Bismuthine, tris(4-methylphenyl)-

Cc1ccc(cc1)[Bi](c1ccc(cc1)C)c1ccc(cc1)C Request for Quotation
Chemical Name: Bismuthine, tris(4-methylphenyl)-
CAS Number: 5142-75-6
Product Number: AG003V6K(AGN-PC-0JMDHK)
Synonyms:
MDL No:
Molecular Formula: C21H21Bi
Molecular Weight: 482.37184

Identification/Properties

Properties
MP:
119℃
Form:
Solid
Computed Properties
Molecular Weight:
482.379g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
3
Exact Mass:
482.145g/mol
Monoisotopic Mass:
482.145g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
263
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tri-p-tolylbismuthine is a versatile chemical compound that finds wide applications in chemical synthesis. As a bismuth-containing reagent, it serves as a key building block in various organic transformations. One of its primary uses is as a nucleophilic catalyst in cross-coupling reactions, where it facilitates the formation of carbon-carbon or carbon-heteroatom bonds. Additionally, Tri-p-tolylbismuthine can be employed in the synthesis of functionalized organic molecules, including pharmaceutical intermediates and complex natural products. Its unique structure and reactivity make it a valuable tool for organic chemists seeking to access novel chemical structures and execute challenging bond-forming reactions.