13125-59-2

Upstream product

• 67-56-1 methanol 
• 873-49-4 cyclopropylbenzene 
• 55955-55-0 methyl 3-chloro-3-phenylpropyl ether 
• 772-00-9 4-phenyl-1,3-dioxane 
• 16277-67-1 3-methoxy-1-phenylpropene 
• 40685-20-9 (E)-3-methoxy-1-phenylprop-2-en-1-one 
• 24808-73-9 (E)-(3-methoxyprop-1-en-1-yl)benzene 
• 100-42-5 styrene 
• 98-88-4 benzoyl chloride 
• 127618-32-0 2-Diazo-3-methoxy-1-phenylpropanone 
• 55563-72-9 3-methoxy-1-phenylpropan-1-one 

Downstream Products

• 21254-96-6 1--1-phenyl-3-methoxy-propan 
• 18344-91-7 1--1-phenyl-3-methoxy-propan 
• 1605319-69-4 1-azido-3-methoxy-1-phenylpropane 
• 26278-67-1 1,3-dimethoxy-1-phenylpropane 
• 55563-71-8 Ethyl(2-methoxyethyl)phenylmethanol 
• 137040-14-3 2-Hydroxy-4-methoxy-2-phenyl-butyric acid 1-aza-bicyclo[2.2.2]oct-3-yl ester 
• 137039-86-2 4-Methoxy-2-phenyl-2-trimethylsilanyloxy-butyronitrile 
• 137040-07-4 2-Hydroxy-4-methoxy-2-phenyl-butyric acid ethyl ester 
• 137039-93-1 2-Hydroxy-4-methoxy-2-phenyl-butyramide 
• 137040-00-7 2-Hydroxy-4-methoxy-2-phenyl-butyric acid 
• 88241-49-0 8-methoxy-4-methyl-6-phenyl-3-(1'-phenylcyclopropyl)(2,4,5-D₃)octa-2,5-diene 
• 79012-25-2 8-methoxy-4-methyl-6-phenyl-3-(1'-phenylcyclopropyl)octa-2,5-diene 
• 88241-50-3 (4-D)(E)-1-methoxy-3-phenylhex-4-en-3-ol 
• 88241-51-4 (5-D)(E)-1-methoxy-3-phenylhex-4-en-3-ol 

Relevant academic research and scientific papers

COMPOSITIONS AND METHODS FOR MODULATING LPA RECEPTORS

The present invention relates to compounds of Formula (1), or pharmaceutically acceptable salts thereof and their pharmaceutical compositions, wherein variables are as defined herein, which are useful as modulators of the activity of lysophosphatidic acid (LPA).

Pentacoordinate vs. Tetracoordinate complexation for alkoxycarbonyl compounds with dialkylboron triflates and trifluoroacetates?

The implication of hitherto unknown pentacoordinate complex formation for alkoxycarbonyl compounds with Et2BX (X =OTf, OCOCF3) is presented by several reduction/allylation experiments and low-temperature 13C, 11

One-Pot Preparation of Alcohols from Aromatic Olefins and Acrylic Acid Derivatives by Cobalt(II) Porphyrin-Catalyzed Reductive Oxygenation Followed by Reduction with Trimethyl Phosphite

Various aromatic olefins and acrylic acid derivatives were converted to benzyl alkohols and α-hydroxyalkanoic acid derivatives in good yields by the reductive oxygenation with oxygen and triethylsilane in the presence of catalytic amount of cobalt(II) porphyrin followed by treating the reaction mixture with trimethyl phosphite.

Cobalt(II) Porphyrin-Catalyzed Oxidation of Olefins to Ketones with Molecular Oxygen and Triethylsilane in 2-Propanol

An efficient conversion of olefins to ketones was achieved by the use of molecular oxygen and triethylsilane in the presence of a catalytic amount of cobalt(II) complex of porphyrin.The oxidation was accelerated remarkably in alcohols and had chomoselectivity for conjugated olefins.

Synthesis and Muscarinic Cholinergic Receptor Affinities of 3-Quinuclidinyl α-(Alkoxyalkyl)-α-aryl-α-hydroxyacetates

Seven analogues of 3-quinuclidinyl benzilate (QNB) in which one phenyl ring was replaced by an alkoxyalkyl moiety were synthesized and their affinities for the muscarinic cholinergic receptor determined.An oxygen in the β-position of the moienty was not w

9,10-DICYANOANTHRACENE-SENSITIZED TWO-ELECTRON OXIDATION OF PHENYLCYCLOPROPANE AND AROMATIC OLEFINS IN THE PRESENCE OF COPPER(II) ION

The photooxidation of phenylcyclopropane, styrene, and indene using 9,10-dicyanoanthracene-Cu(BF4)2 sensitizer system in acetonitrile-alcohol (3:1) solutions affords the corresponding 1,3-dialkoxy and 1,2-dialkoxy compounds.