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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)-

Phosphonium, [(2-nitrophenyl)methyl]triphenyl-, bromide

[O-][N+](=O)c1ccccc1C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-] Request for Quotation
Chemical Name: Phosphonium, [(2-nitrophenyl)methyl]triphenyl-, bromide
CAS Number: 23308-83-0
Product Number: AG002MVC(AGN-PC-0NC8FU)
Synonyms:
MDL No:
Molecular Formula: C25H21BrNO2P
Molecular Weight: 478.3175

Identification/Properties

Properties
MP:
238-240°C
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
478.326g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
477.049g/mol
Monoisotopic Mass:
477.049g/mol
Topological Polar Surface Area:
45.8A^2
Heavy Atom Count:
30
Formal Charge:
0
Complexity:
470
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(2-Nitrobenzyl)triphenylphosphonium bromide is a versatile compound utilized in chemical synthesis for various applications. This compound, known for its unique properties, serves as an efficient reagent in organic transformations. Its ability to undergo nucleophilic substitution reactions allows for the introduction of the (2-Nitrobenzyl) functionality into organic molecules. Additionally, the triphenylphosphonium moiety enhances the stability and reactivity of the compound, making it a valuable tool in synthetic chemistry. The (2-Nitrobenzyl) group can be selectively cleaved under mild conditions, providing a strategic entry point for further functionalization and derivatization. Its utility extends to the synthesis of pharmaceutical intermediates, natural product analogs, and advanced materials.