59725-01-8

Usage

Uses

Bromo(pentyl)triphenylphosphorane was used as a catalyst in phase-transfer catalysis study.

InChI:InChI=1/C23H26BrP/c1-2-3-13-20-25(24,21-14-7-4-8-15-21,22-16-9-5-10-17-22)23-18-11-6-12-19-23/h4-12,14-19H,2-3,13,20H2,1H3

Upstream product

• 110-53-2 1-Bromopentane 
• 603-35-0 triphenylphosphine 

Downstream Products

• 38372-49-5 undec-6-en-2-one 
• 132124-52-8 (Z)-4-Nonenylchlorid 
• 148311-91-5 (Z)-1-Cyclopropyl-1-hexen 
• 152561-57-4 (+)-3α-(2Z-heptenyl)-2β-triphenylmethoxymethyl-1α,4α-cyclopentanediol 
• 89790-28-3 1-(p-cyanophenyl)hexene-1 
• 29147-95-3 1-(p-cyanophenyl)hexane 
• 376640-08-3 (4-hexylphenyl)methylamine 
• 89790-10-3 N-(p-hexylbenzyl)formamide 
• 51652-47-2 (Z)-dec-5-en-1-ol 
• 67446-07-5 (Z)-5-decenyl acetate 
• 58701-06-7 (6E,11Z)-6,11-hexadecadien-1-al 

Relevant academic research and scientific papers

Design of Inhibitors from the Three-Dimensional Structure of Alcohol Dehydrogenase. Chemical Synthesis and Enzymatic Properties

Inhibitors of liver alcohol dehydrogenase were designed from the three-dimensional structure of the enzyme.The ligand to the catalytic zinc ion is an amide group or, better, a formamide group.With the latter function, a hydrogen bond between the NH group and the hydroxyl group of Ser-48 may be formed.The hydrophobic substrate binding site brings structural restraints. α-ω bifunctional molecules show good inhibitory properties possibly due to the interactions with polar residues at the entrance of the substrate binding site.