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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)-

4-Chloroisoindoline hydrochloride

Clc1cccc2c1CNC2.Cl Request for Quotation
Chemical Name: 4-Chloroisoindoline hydrochloride
CAS Number: 924304-73-4
Product Number: AG0038JA(AGN-PC-0687VH)
Synonyms:
MDL No:
Molecular Formula: C8H9Cl2N
Molecular Weight: 190.0698

Identification/Properties

Computed Properties
Molecular Weight:
190.067g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
189.011g/mol
Monoisotopic Mass:
189.011g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
126
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloroisoindoline hydrochloride is a versatile chemical compound widely used in chemical synthesis processes. It serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. With its unique structure and reactivity, 4-Chloroisoindoline hydrochloride plays a crucial role in the development of novel molecules with diverse applications. Chemists often rely on this compound as a strategic starting material for the synthesis of complex organic compounds due to its ability to undergo multiple types of chemical reactions, such as nucleophilic substitution, cyclization, and cross-coupling reactions. In the realm of medicinal chemistry, 4-Chloroisoindoline hydrochloride is frequently employed in the preparation of drug candidates and lead compounds targeting various therapeutic areas. Additionally, its utility extends to the synthesis of advanced materials and fine chemicals, highlighting its significance as a valuable tool in modern chemical research and development.