4596-96-7

Upstream product

• 4596-95-6 bis(biphenyl-4-yl)methanol 
• 92-66-0 4-bromo-1,1'-biphenyl 

Downstream Products

• 14704-25-7 2-Chlor-1-m-biphenylyl-1,1-bis(p-biphenylyl)ethan 
• 124419-97-2 2-Brom-1,1,3,3-tetra(4-biphenylyl)-1-propen 
• 124419-73-4 1,1,3,3-Tetra(4-biphenylyl)allen 
• 176713-96-5 (Bis-biphenyl-4-yl-methyl)-phosphonic acid diethyl ester 
• 14704-22-4 1,1,2,2-tetrakis-biphenyl-4-yl-ethane 
• 14704-23-5 m-Biphenylylbis(p-biphenylyl)methan 
• 124419-89-2 1,1,3,3-Tetra(4-biphenylyl)-1-propen 

Relevant academic research and scientific papers

Synthesis and photoluminescent properties of new ceramidine derivatives

A series of new ceramidine derivatives 8a-f has been synthesized in 4-5 steps involving a Wittig reaction of ceramidonine with various triphenylphosphonium bromides. Their UV and photoluminescence (PL) properties are reported. The compounds showed medium to strong PL between 502 and 522 nm at a concentration of 1 × 10-5 M CH2Cl2.

Benzylphosphonic acid inhibitors of human prostatic acid phosphatase

A series of α-substituted benzylphosphonic acids is described as inhibitors of human prostatic acid phosphatase, an enzyme has been used as a model to study aryl phosphatases. The most potent inhibitors in this series are 2-trifluoromethylbenzhydrylphosphonic acid (9 μM), and α-(2-phenylethyl)benzylphosphonic acid (14 μM). The structure-activity studies suggest that bulk tolerance beyond the phosphate binding area limits the steric or hydrophobic contribution to inhibitor potency achieved through α-carbon substitution.