132483-77-3

Basic information

• Product Name: Propanedioic acid, (4-cyanophenyl)methyl-, diethyl ester
• CAS NO: 132483-77-3
• Molecular Formula: C15H17NO4
• Molecular Weight: 275.304
• Mol File: 132483-77-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Propanedioic acid, (4-cyanophenyl)methyl-, diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Propanedioic acid, (4-cyanophenyl)methyl-, diethyl ester(132483-77-3)
• EPA Substance Registry System: Propanedioic acid, (4-cyanophenyl)methyl-, diethyl ester(132483-77-3)

Safety Data

• Hazardous Substances Data: 132483-77-3(Hazardous Substances Data)

Upstream product

• 609-08-5 Diethyl methylmalonate 
• 100-00-5 4-chlorobenzonitrile 
• 61881-49-0 Diethyl 2-methyl-2-(4-nitrophenyl)malonate 
• 1194-02-1 4-fluorobenzonitrile 
• 61881-50-3 amino-4-phenyl methyl malonate d'ethyle 
• 13682-73-0 Potassium dicyanocuprate 

Downstream Products

• 132483-32-0 2-<4-(Thiazol-2-yl)phenyl>propionic Acid 
• 132483-43-3 2-[4-(5-Methyl-thiazol-2-yl)-phenyl]-propionic acid 
• 132483-42-2 2-<4-(4-Methylthiazol-2-yl)phenyl>propionic Acid 
• 138568-67-9 2-[4-(5-Ethyl-thiazol-2-yl)-phenyl]-propionic acid 
• 132483-47-7 2-[4-(4-Ethyl-thiazol-2-yl)-phenyl]-propionic acid 
• 132483-44-4 2-<4-(4-Vinylthiazol-2-yl)phenyl>propionic Acid 
• 132483-46-6 2-[4-(4,5-Dimethyl-thiazol-2-yl)-phenyl]-propionic acid 
• 138568-65-7 2-<4-(4-Hydroxymethylthiazol-2-yl)phenyl>propionic Acid 
• 138568-64-6 2-<4-(4-Allylthiazol-2-yl)phenyl>propionic Acid 
• 132483-55-7 2-[4-(4-Butyl-thiazol-2-yl)-phenyl]-propionic acid 
• 132483-61-5 2-[4-(4-Acetyl-thiazol-2-yl)-phenyl]-propionic acid 
• 138568-63-5 2-[4-(4-Isopropyl-thiazol-2-yl)-phenyl]-propionic acid 
• 138568-66-8 2-<4-(4-Methoxymethylthiazol-2-yl)phenyl>propionic Acid 
• 138568-68-0 2-[4-(4-Ethyl-5-methyl-thiazol-2-yl)-phenyl]-propionic acid 

Relevant articles and documents

Nucleophilic aromatic substitution using Et3SiH/cat. t-Bu-P4 as a system for nucleophile activation

A novel type of deprotonative arylation of nucleophiles was conducted using Et3SiH/cat. t-Bu-P4 and the powerful SNAr reactions of aryl fluorides were accomplished using alcohols and malonates as nucleophiles. The Royal Society of Ch