111373-31-0

Basic information

• Product Name: diethyl (2-iodobenzyl)malonate
• Synonyms: diethyl (2-iodobenzyl)malonate
• CAS NO: 111373-31-0
• Molecular Weight: 376.191
• Mol File: 111373-31-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: diethyl (2-iodobenzyl)malonate(CAS DataBase Reference)
• NIST Chemistry Reference: diethyl (2-iodobenzyl)malonate(111373-31-0)
• EPA Substance Registry System: diethyl (2-iodobenzyl)malonate(111373-31-0)

Safety Data

• Hazardous Substances Data: 111373-31-0(Hazardous Substances Data)

Upstream product

• 996-82-7 sodium diethylmalonate 
• 59473-45-9 2-(chloromethyl)iodobenzene 
• 183789-20-0 2-iodobenzyl methanesulfonate 
• 533-58-4 2-Iodophenol 
• 105-53-3 diethyl malonate 
• 5159-41-1 2-iodobenzyl alcohol 

Downstream Products

• 119826-73-2 (E)-5,5-Bis-ethoxycarbonyl-6-(2-iodo-phenyl)-hex-2-enoic acid ethyl ester 
• 122951-06-8 ethyl 3-(2-iodophenyl)propanoate 
• 169626-71-5 5,5,10,10-tetrakis(ethoxycarbonyl)-11-(2'-iodophenyl)-1-undecene 
• 169626-63-5 5,5,18,18-tetrakis(ethoxycarbonyl)-19-(2'-iodophenyl)-1,2-nonadecadiene 
• 169626-72-6 5,5,18,18-tetrakis(ethoxycarbonyl)-19-(2'-iodophenyl)-1-nonadecene 
• 1429337-71-2 1-(phenyl)-6,7-dihydro-5H-benzo[c][1,2,3]triazolo[1,5-a]azepine 
• 1429337-72-3 1-(4-methoxyphenyl)-6,7-dihydro-5H-benzo[c]-[1,2,3]triazolo[1,5-a]azepine 
• 1429337-73-4 1-(4-nitrophenyl)-6,7-dihydro-5H-benzo[c][1,2,3]triazolo[1,5-a]azepine 
• 1429337-74-5 1-(2,4-dimethoxypyrimidin-5-yl)-6,7-dihydro-5H-benzo[c][1,2,3]triazolo[1,5-a]azepine 
• 1429337-75-6 1-({(3aR,5R,6S,6aR)-5-[(R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyltetrahydrofuro[3,2-d][1,3]dioxol-6-yl-oxy}methyl)-6,7-dihydro-5H-benzo[c][1,2,3]triazolo[1,5-a]azepine 
• 1429337-87-0 1-(3-azidopropyl)-2-iodobenzene 
• 181717-14-6 3-(2-iodophenyl)propyl methanesulfonate 

Relevant articles and documents

Harnessing [1,4], [1,5], and [1,6] Anionic Fries-type Rearrangements by Reaction-Time Control in Flow

A series of anionic Fries-type rearrangements of carbamoyl-substituted aryllithium intermediates were controlled by using flow microreactor systems. For the [1,4] and [1,5] rearrangements, the aryllithium intermediate formed before carbamoyl migration and

AROMATIC OXYPHENYL AND AROMATIC SYLFANYLPHENYL DERIVATIVES

The present invention relates to compounds of formula I wherein the substituents are as defined below. The compounds of formula I are useful for the treatment of diseases such as schizophrenia, including both the positive and the negative symptoms of schizophrenia and other psychoses.