4-Amino-2-mercapto-phenol Hydrochloride|98140-58-0,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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-Amino-2-mercapto-phenol Hydrochloride

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Chemical Name:	4-Amino-2-mercapto-phenol Hydrochloride
CAS Number:	98140-58-0
Product Number:	AG01E4T2(AGN-PC-0WAIMJ)
Synonyms:
MDL No:
Molecular Formula:	C6H8ClNOS
Molecular Weight:	177.65182

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Chemical Structure

4-Amino-2-mercaptophenol Hydrochloride is a versatile compound widely used in chemical synthesis for various applications. In organic chemistry, it serves as a key building block for the synthesis of dyes, pigments, and pharmaceuticals. Due to its unique structure and reactivity, this compound is particularly valuable in the development of complex organic molecules. By incorporating 4-Amino-2-mercaptophenol Hydrochloride into reactions, chemists can introduce specific functional groups and modify the properties of target compounds. Its sulfur-containing moiety also makes it a valuable tool in metal coordination chemistry, where it can act as a chelating agent to form stable complexes with metal ions. Furthermore, the presence of the amino group enables the compound to participate in various types of chemical reactions, including nucleophilic substitution and condensation reactions, expanding its utility in synthetic chemistry.