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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)-

1H-Isoindole, 4-bromo-2,3-dihydro-2-(phenylmethyl)-

Brc1cccc2c1CN(C2)Cc1ccccc1 Request for Quotation
Chemical Name: 1H-Isoindole, 4-bromo-2,3-dihydro-2-(phenylmethyl)-
CAS Number: 923590-78-7
Product Number: AG00IH3U(AGN-PC-09MQXT)
Synonyms:
MDL No:
Molecular Formula: C15H14BrN
Molecular Weight: 288.1824

Identification/Properties

Properties
BP:
354.0±42.0°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Benzyl-4-bromoisoindoline, also known as $name$, is a versatile compound frequently employed in chemical synthesis as a key building block in organic chemistry. Due to its unique structure and reactivity, this compound plays a crucial role in various synthetic processes, particularly in the formation of complex organic molecules.One of the primary applications of 2-Benzyl-4-bromoisoindoline is in the synthesis of heterocyclic compounds, which are essential in drug discovery and material science. The presence of the bromo group makes it a useful precursor for introducing different functional groups through selective substitution reactions, allowing chemists to tailor the properties of the final products.Furthermore, 2-Benzyl-4-bromoisoindoline can serve as a starting material for the construction of biologically active molecules, such as pharmaceuticals and agrochemicals. Its structural motif provides a scaffold for further modifications, enabling the creation of diverse molecular libraries for screening purposes in drug development.Overall, the strategic incorporation of 2-Benzyl-4-bromoisoindoline into synthetic pathways offers chemists a powerful tool for the efficient and precise assembly of intricate organic compounds with tailored properties and functionalities.