4-Amino-2,6-diphenylphenol, with the CAS number 50432-01-4, is an organic compound characterized by the presence of an amino group and two phenyl groups attached to a phenolic structure. This compound typically exhibits a solid form at room temperature and is known for its potential applications in various fields, including dye chemistry and as an intermediate in organic synthesis. The presence of the amino group contributes to its basicity and reactivity, allowing it to participate in various chemical reactions, such as electrophilic substitutions. Additionally, the diphenyl substitution enhances its stability and may influence its solubility in organic solvents. The compound may also exhibit specific optical properties, making it of interest in materials science. Safety data should be consulted, as with any chemical, to understand its handling, toxicity, and environmental impact. Overall, 4-amino-2,6-diphenylphenol is a versatile compound with significant implications in both industrial and research applications.

4-amino-2,6-diphenylphenol

50432-01-4: Aminodiphenylphenol, 5'-Amino-1,1':3',1''-Terphenyl-2'-Ol

5'-Amino-[1,1':3',1''-terphenyl]-2'-ol

4-Amino-2,6-diphenylphenol

5'-Amino-[1,1':3',1''-terphenyl]-2'-ol is an analog of Δ9-tetrahydrocannabinol that was synthesized as a probe for the detection of glutathione. This compound is electrochemically oxidized to δ9-tetrahydrocannabinol. The oxidation reaction is monitored by measuring the change in current at the electrode in response to changes in redox potential. 5'-Amino-[1,1':3',1''-terphenyl]-2'-ol undergoes pyrolysis and can be used as a probe for acetaminophen.

5Õ-Amino-[1,1Õ:3Õ,1ÕÕ-Terphenyl]-2Õ-Ol

CAS 50432-01-4: 4-amino-2,6-diphenylphenol

5'-Amino-[1,1':3',1''-terphenyl]-2'-ol

Ref: IN-DA003MC1

4-Amino-2,6-diphenylphenol

Ref: 3B-A1269

5'-Amino-[1,1':3',1''-terphenyl]-2'-ol

Ref: 10-F222834

5'-Amino-[1,1':3',1''-terphenyl]-2'-ol

Ref: 3D-ACA43201

5Õ-Amino-[1,1Õ:3Õ,1ÕÕ-Terphenyl]-2Õ-Ol

Ref: 54-OR1027256