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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)-

2-(3-aminopropyl)isoindole-1,3-dione;hydrochloride

NCCCN1C(=O)c2c(C1=O)cccc2.Cl Request for Quotation
Chemical Name: 2-(3-aminopropyl)isoindole-1,3-dione;hydrochloride
CAS Number: 121821-01-0
Product Number: AG00163A(AGN-PC-00181X)
Synonyms:
MDL No:
Molecular Formula: C11H13ClN2O2
Molecular Weight: 240.6861

Identification/Properties

Computed Properties
Molecular Weight:
240.687g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
240.067g/mol
Monoisotopic Mass:
240.067g/mol
Topological Polar Surface Area:
63.4A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
254
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:
H319
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(3-Aminopropyl)isoindoline-1,3-dione hydrochloride is a versatile compound widely used in chemical synthesis as a key intermediate in the production of complex organic molecules. Its unique structure and reactivity make it particularly valuable in the preparation of functionalized derivatives for medicinal chemistry research and pharmaceutical development. This compound serves as a crucial building block for the synthesis of various heterocyclic compounds, which are essential in the creation of biologically active compounds and drug candidates. Additionally, its amine functionality allows for further derivatization, enabling the introduction of different substituents to modulate the physicochemical properties of the resulting compounds. In synthesis, 2-(3-Aminopropyl)isoindoline-1,3-dione hydrochloride offers chemists a powerful tool to access novel chemical entities with potential applications in drug discovery and material science.