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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)-

1-Benzothiophen-7-amine hydrochloride

Nc1cccc2c1scc2.Cl Request for Quotation
Chemical Name: 1-Benzothiophen-7-amine hydrochloride
CAS Number: 1423026-20-3
Product Number: AG01A1ZY(AGN-PC-0WAIZG)
Synonyms:
MDL No:
Molecular Formula: C8H8ClNS
Molecular Weight: 185.6738

Identification/Properties

Computed Properties
Molecular Weight:
185.669g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
185.007g/mol
Monoisotopic Mass:
185.007g/mol
Topological Polar Surface Area:
54.3A^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


1-Benzothiophen-7-amine hydrochloride is a versatile compound widely utilized in chemical synthesis for various applications. In organic chemistry, it serves as a key building block for the synthesis of a wide range of pharmaceuticals, agrochemicals, and functional materials.Its unique structure and reactivity make it a particularly valuable intermediate in the development of novel therapeutic agents. Through strategic modification of the amine group and thiophene ring, researchers can access diverse chemical scaffolds with potential biological activity. Additionally, the presence of the hydrochloride salt enhances its solubility in polar solvents, facilitating its use in reaction mixtures.Furthermore, 1-Benzothiophen-7-amine hydrochloride plays a crucial role in the formation of heterocyclic compounds, which are prevalent in drug discovery and materials science. By participating in cyclization reactions, it enables the construction of complex frameworks with desirable properties. This compound's versatile nature and synthetic utility make it a valuable tool for advancing scientific research and innovation in the field of organic chemistry.