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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)-

Benzenemethanol, 4-amino-3-chloro-

OCc1ccc(c(c1)Cl)N Request for Quotation
Chemical Name: Benzenemethanol, 4-amino-3-chloro-
CAS Number: 113372-69-3
Product Number: AG008UA2(AGN-PC-00O76A)
Synonyms:
MDL No:
Molecular Formula: C7H8ClNO
Molecular Weight: 157.59752

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Chemical Structure


The compound (4-Amino-3-chlorophenyl)methanol plays a crucial role in chemical synthesis as a versatile building block for various organic reactions. Due to its unique structure, it serves as a key intermediate in the synthesis of pharmaceutical compounds, agrochemicals, and materials science applications. Its primary amine and hydroxyl functional groups enable it to participate in a wide range of reactions, including condensation, alkylation, and oxidation processes. Additionally, this compound can be used as a chiral auxiliary in asymmetric synthesis, allowing for the creation of enantiomerically pure molecules. Its significance in the synthesis of diverse chemical compounds makes it a valuable tool for researchers and organic chemists seeking to access novel structures and functional materials.