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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-Inden-2-amine, 5-chloro-2,3-dihydro-

NC1Cc2c(C1)cc(cc2)Cl Request for Quotation
Chemical Name: 1H-Inden-2-amine, 5-chloro-2,3-dihydro-
CAS Number: 73536-83-1
Product Number: AG00FH8Z(AGN-PC-02R8LM)
Synonyms:
MDL No:
Molecular Formula: C9H10ClN
Molecular Weight: 167.6354

Identification/Properties

Computed Properties
Molecular Weight:
167.636g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
167.05g/mol
Monoisotopic Mass:
167.05g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
149
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, 5-Chloro-2,3-dihydro-1H-inden-2-amine serves as a versatile building block for the creation of various organic compounds. Due to its unique structure and reactivity, this compound is commonly utilized as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals.The presence of the chlorine atom at the 5-position of the indene ring enables specific functionalization reactions, allowing chemists to introduce a wide range of substituents at this site. This capability makes 5-Chloro-2,3-dihydro-1H-inden-2-amine a valuable precursor for the synthesis of diverse molecules with tailored properties and functionalities.Moreover, the amino group present in the structure of this compound provides further synthetic versatility, enabling the formation of amine derivatives through various transformation processes. These amine derivatives can be further modified or subjected to additional functionalization steps to generate complex molecular structures with desired characteristics.Overall, the strategic placement of the chlorine atom and amino group in 5-Chloro-2,3-dihydro-1H-inden-2-amine makes it a valuable reagent for the efficient synthesis of advanced organic compounds with applications across multiple industries.