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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)-

5-Chloroisoindoline hydrochloride

Clc1ccc2c(c1)CNC2.Cl Request for Quotation
Chemical Name: 5-Chloroisoindoline hydrochloride
CAS Number: 912999-79-2
Product Number: AG0036SI(AGN-PC-088Q1P)
Synonyms:
MDL No: MFCD11223562
Molecular Formula: C8H9Cl2N
Molecular Weight: 190.0698

Identification/Properties

Properties
Storage:
Room Temperature;
Form:
Solid
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


5-Chloroisoindoline hydrochloride is a versatile chemical compound commonly utilized in various chemical synthesis applications. Its unique properties make it a valuable reagent in organic chemistry processes, particularly in the development of pharmaceuticals, agrochemicals, and functional materials. One of the key applications of 5-Chloroisoindoline hydrochloride is its role as a precursor in the synthesis of heterocyclic compounds, which are essential building blocks in drug discovery and development. With its ability to introduce a chloro functional group into organic molecules, 5-Chloroisoindoline hydrochloride serves as a valuable tool for chemists looking to modify and optimize the properties of complex organic structures. Furthermore, its reactivity and compatibility with a wide range of reaction conditions make it a popular choice for researchers seeking to access novel chemical entities through creative synthetic strategies.