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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-1,3(2H)-dione, 2-(4-chlorophenyl)-

O=C1N(c2ccc(cc2)Cl)C(=O)c2c1cccc2 Request for Quotation
Chemical Name: 1H-Isoindole-1,3(2H)-dione, 2-(4-chlorophenyl)-
CAS Number: 7386-21-2
Product Number: AG003SCB(AGN-PC-0JLTJ6)
Synonyms:
MDL No:
Molecular Formula: C14H8ClNO2
Molecular Weight: 257.6718

Identification/Properties

Computed Properties
Molecular Weight:
257.673g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
257.024g/mol
Monoisotopic Mass:
257.024g/mol
Topological Polar Surface Area:
37.4A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
339
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(4-Chlorophenyl)isoindoline-1,3-dione, commonly known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound serves as a valuable building block in the creation of various organic molecules due to its unique structural properties and reactivity.One prominent application of $name$ in chemical synthesis is its use as a key intermediate in the production of heterocyclic organic compounds. By incorporating this compound into synthetic routes, chemists can access a diverse range of molecular structures with potential applications in pharmaceuticals, agrochemicals, and materials science.Furthermore, $name$ can be employed as a starting material for the synthesis of biologically active compounds such as pharmaceuticals and crop protection agents. Its ability to undergo a variety of chemical transformations, including substitution reactions and cyclization processes, makes it a valuable tool for designing and constructing complex molecular architectures.Overall, the use of 2-(4-Chlorophenyl)isoindoline-1,3-dione in chemical synthesis offers a pathway to the creation of novel organic molecules with specialized properties and functionalities, making it an essential component in the toolbox of synthetic chemists.