The chemical substance known as 2H-1-Benzopyran-2-one, 3-[(1R)-1-(4-chlorophenyl)-3-oxobutyl]-4-hydroxy- is a complex organic compound characterized by its benzopyran structure, which features a fused benzene and pyran ring. This compound contains a hydroxyl group (-OH) at the 4-position, contributing to its potential reactivity and solubility in polar solvents. The presence of a 4-chlorophenyl group and a ketone functional group indicates that it may exhibit significant biological activity, possibly as a pharmaceutical agent or a bioactive compound. The stereochemistry at the 1-position, denoted as (1R), suggests specific spatial arrangements that can influence the compound's interactions with biological targets. Additionally, the compound's molecular structure implies potential applications in medicinal chemistry, particularly in the development of drugs targeting various diseases. Its CAS number, 95271-89-9, allows for precise identification and retrieval of information regarding its properties, synthesis, and applications in scientific literature.

2H-1-Benzopyran-2-one,3-[(1R)-1-(4-chlorophenyl)-3-oxobutyl]-4-hydroxy-

95271-89-9: The chemical substance known as 2H-1-Benzopyran-2-one, 3-[(1R)-1-(4-chlorophenyl)-3-oxobutyl]-4-hydroxy- is a complex organic compound characterized by its benzopyran structure, which features a fused benzene and pyran ring. This compound contains a hydroxyl group (-OH) at the 4-position, contributing to its potential reactivity and solubility in polar solvents. The presence of a 4-chlorophenyl group and a ketone functional group indicates that it may exhibit significant biological activity, possibly as a pharmaceutical agent or a bioactive compound. The stereochemistry at the 1-position, denoted as (1R), suggests specific spatial arrangements that can influence the compound's interactions with biological targets. Additionally, the compound's molecular structure implies potential applications in medicinal chemistry, particularly in the development of drugs targeting various diseases. Its CAS number, 95271-89-9, allows for precise identification and retrieval of information regarding its properties, synthesis, and applications in scientific literature.

(R)-(+)-Coumachlor

<p>Applications (+)-Coumachlor is an internal standard in the analysis of the rodenticide Warfarin.<br>References Dikshith, T., et al.: J. Exp. Biol., 29, 149 (1991);<br></p>

CAS 95271-89-9

2H-1-Benzopyran-2-one,3-[(1R)-1-(4-chlorophenyl)-3-oxobutyl]-4-hydroxy-

(R)-(+)-Coumachlor

Ref: 4Z-C-001003

(+)-Coumachlor

Ref: TR-C725055