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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-chloro-2,3-dihydro-1H-indole;hydrochloride

Clc1ccc2c(c1)CCN2.Cl Request for Quotation
Chemical Name: 5-chloro-2,3-dihydro-1H-indole;hydrochloride
CAS Number: 1013398-58-7
Product Number: AG00048Z(AGN-PC-0BS6OT)
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


5-Chloroindoline hydrochloride serves as a versatile building block in chemical synthesis, particularly in the realm of organic chemistry. Its incorporation in various reactions allows for the generation of diverse molecular structures with potential utility in pharmaceuticals, agrochemicals, and materials science. The presence of the chloro group provides a handle for further functionalization, enabling the introduction of additional chemical moieties to tailor the properties of the final product. Additionally, the indoline scaffold offers structural complexity and potential biological activity, making it a valuable starting material for the synthesis of bioactive compounds and heterocyclic derivatives. By judiciously manipulating the reactivity of 5-Chloroindoline hydrochloride through different synthetic methodologies, chemists can access a wide array of novel molecules with unique properties and applications.