41140-53-8

Basic information

• Product Name: 1-Methanesulfonyloxy-3,3-diphenylpropane
• Synonyms: 1-Methanesulfonyloxy-3,3-diphenylpropane
• CAS NO: 41140-53-8
• Molecular Weight: 290.383
• Mol File: 41140-53-8.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 1-Methanesulfonyloxy-3,3-diphenylpropane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Methanesulfonyloxy-3,3-diphenylpropane(41140-53-8)
• EPA Substance Registry System: 1-Methanesulfonyloxy-3,3-diphenylpropane(41140-53-8)

Safety Data

• Hazardous Substances Data: 41140-53-8(Hazardous Substances Data)

Upstream product

• 23426-03-1 3,3-diphenylpropanoic acid methyl ester 
• 606-83-7 3,3-Diphenylpropionic acid 
• 7476-18-8 3,3-diphenyl-propionic acid ethyl ester 
• 4801-14-3 3,3-diphenylprop-2-en-1-ol 
• 17792-17-5 ethyl 3,3-diphenylacrylate 
• 119-61-9 benzophenone 
• 20017-67-8 3,3-diphenylpropan-1-ol 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 199938-12-0 N-(3,3-diphenylpropyl)homopiperazine 
• 199935-06-3 1-benzyl-4-(3,3-diphenylpropyl)homopiperazine 
• 199935-14-3 1-(3,3-Diphenylpropyl)-4-(4-nitrobenzyl)homopiperazine 
• 199935-21-2 4-[4-(3,3-diphenyl-propyl)-[1,4]diazepan-1-ylmethyl]-benzonitrile 
• 201043-33-6 4-(3,3-DIPHENYLPROPOXY)BROMOBENZENE 
• 1404063-64-4 (S)-1-(3,3-diphenylpropyl)-3-methylpyrrolidin-3-ol 
• 1404062-92-5 (S)-3-[(S)-1-(3,3-diphenylpropyl)-3-methylpyrrolidin-3-yl] 5-methyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate 
• 1404062-76-5 3-[1-(3,3-diphenylpropyl)-3-methylpyrrolidin-3-yl] 5-methyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate 
• 1404063-63-3 1-(3,3-diphenylpropyl)-3-methylpyrrolidin-3-ol 
• 20974-36-1 4-(3,3-diphenyl-1-propyl)piperazine 

Relevant articles and documents

Selective Pd-catalyzed hydrogenation of 3,3-diphenylallyl alcohol: Efficient synthesis of 3,3-diarylpropylamine drugs diisopromine and feniprane

The Pd-catalyzed selective hydrogenation of C[dbnd]C double bond in (3,3-diphenylallyl)diisopropylamine or 3,3-diphenylallyl alcohol was evaluated using different catalytic systems [Pd/C, Pd(OAc)2/ionic liquid, isolated Pd(0) nanoparticles]. For the (3,3-diphenylallyl)diisopropylamine, hydrogenolysis is preferred over hydrogenation, and only moderate selectivities were obtained for the desired product. However, complete conversion and 100% selectivity were obtained for the hydrogenation of 3,3-diphenylallyl alcohol using isolated Pd(0) nanoparticles under mild condition. This successful strategy enabled the effective synthesis of diisopromine and feniprane drugs and opens new possibilities for the preparation of other biologically active compounds.

1,4-dihydropyridine-3,5-dicarboxylate Derivatives And Preparation And Use Thereof

The present invention relates to a 1,4-dihydropyridine-3,5-dicarboxylate compound of general compound (I), a process for preparing the same, a use thereof for the manufacture of a medicament for treating and/or preventing kidney injury, cardiovascular diseases and/or endocrine diseases, as well as a pharmaceutical composition and a pharmaceutical formulation containing said compounds, wherein the definitions of R1, R2, R3, R4, R5, R6, R7, R8, m, n1, n2, p and q are the same as those defined in the description.

Synthesis and evaluation of 4-substituted piperidines and piperazines as balanced affinity μ opioid receptor (MOR) agonist/δ opioid receptor (DOR) antagonist ligands

In this letter, we describe a series of 4-substituted piperidine and piperazine compounds based on tetrahydroquinoline 1, a compound that shows balanced, low nanomolar binding affinity for the mu opioid receptor (MOR) and the delta opioid receptor (DOR).