141273-91-8

Basic information

• Product Name: Benzenepropanoic acid, 2-iodo-, methyl ester
• CAS NO: 141273-91-8
• Molecular Formula: C10H11IO2
• Molecular Weight: 290.101
• Mol File: 141273-91-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenepropanoic acid, 2-iodo-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanoic acid, 2-iodo-, methyl ester(141273-91-8)
• EPA Substance Registry System: Benzenepropanoic acid, 2-iodo-, methyl ester(141273-91-8)

Safety Data

• Hazardous Substances Data: 141273-91-8(Hazardous Substances Data)

Upstream product

• 1234562-76-5 C₉H₇IN₂O 
• 67-56-1 methanol 
• 96606-95-0 3-(2-iodophenyl)propanoic acid 
• 66191-86-4 3-(2-bromophenyl)propanoic acid,methyl ester 
• 26260-02-6 2-iodobenzaldehyde 
• 40888-21-9 methyl (E)-3-(2′-iodophenyl)acrylate 
• 15115-58-9 3-(2-bromophenyl)propionic acid 

Downstream Products

• 1318792-90-3 methyl 3-{2-[4-hydroxy-3-(hydroxymethyl)-1-butynyl]phenyl}propanoate 
• 1318792-91-4 methyl 3-[2-(4-hydroxy-3-{[(4-methoxybenzyl)oxy]methyl}-1-butynyl)phenyl]propanoate 
• 1318792-92-5 3-[2-(4-hydroxy-3-{[(4-methoxybenzyl)oxy]methyl}-1-butynyl)phenyl]propanoic acid 
• 1402345-89-4 3-(2-iodophenyl)-N-methoxypropanamide 
• 1402345-55-4 3-(2-iodophenyl)-N-methoxy-N-phenylpropanamide 
• 91523-37-4 N-methoxy-3,4-dihydro-1H-quinolin-2-one 
• 96606-95-0 3-(2-iodophenyl)propanoic acid 
• 1421710-54-4 methyl 3-(2-(3-hydroxyprop-1-ynyl)phenyl)propanoate 
• 1421710-52-2 methyl 3-(2-(3-iodoprop-1-ynyl)phenyl)propanoate 
• 1318792-89-0 methyl 3-{2-[2-(2,2-dimethyl-1,3-dioxan-5-yl)ethynyl]phenyl}propanoate 
• 1318792-98-1 methyl 3-(2-{2-[(2S)-1,4-dioxaspiro[4.5]dec-2-yl]ethynyl}phenyl)propanoate 
• 1318793-16-6 (6S)-6-[(4-methoxybenzyl)oxy]-7,8-didehydro-1,2,5,6-tetrahydro-3H-4-benzoxecin-3-one 
• 1318793-13-3 3-(2-{(3S)-4-hydroxy-3-[(4-methoxybenzyl)oxy]-1-butynyl}phenyl)propanoic acid 
• 1318793-10-0 methyl 3-(2-{(3S)-4-hydroxy-3-[(4-methoxybenzyl)oxy]-1-butynyl}phenyl)propanoate 

Relevant articles and documents

Reduction of Electron-Deficient Alkenes Enabled by a Photoinduced Hydrogen Atom Transfer

Direct hydrogen atom transfer from a photoredox-generated Hantzsch ester radical cation to electron-deficient alkenes has enabled the development of an efficient formal hydrogenation under mild, operationally simple conditions. The HAT-driven mechanism is supported by experimental and computational studies. The reaction is applied to a variety of cinnamate derivatives and related structures, irrespective of the presence of electron-donating or electron-withdrawing substituents in the aromatic ring and with good functional group compatibility. (Figure presented.).

First example of an atropselective dehydro-Diels-Alder (ADDA) reaction

A new concept of a stereoselective synthesis of axially chiral biaryls, formed in the course of the dehydro-Diels-Alder (DDA) reaction, has been disclosed. It is based on asymmetric induction of the newly formed chirality axis by a chirality center, which