119770-37-5

Basic information

• Product Name: methyl 4-[(E)-2-methoxyethenyl]benzoate
• Synonyms: methyl 4-[(E)-2-methoxyethenyl]benzoate
• CAS NO: 119770-37-5
• Molecular Weight: 192.214
• Mol File: 119770-37-5.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: methyl 4-[(E)-2-methoxyethenyl]benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4-[(E)-2-methoxyethenyl]benzoate(119770-37-5)
• EPA Substance Registry System: methyl 4-[(E)-2-methoxyethenyl]benzoate(119770-37-5)

Safety Data

• Hazardous Substances Data: 119770-37-5(Hazardous Substances Data)

Upstream product

• 4009-98-7 (methoxymethyl)triphenylphosphonium chloride 
• 1571-08-0 methyl 4-formylbenzoate 
• 67-56-1 methanol 
• 3034-86-4 4-ethynylbenzoic acid methyl ester 

Downstream Products

• 397327-99-0 4-[(E)-2-methoxyethenyl]benzoic acid 
• 106918-32-5 4-carbomethoxyphenylacetaldehyde 
• 1416069-73-2 (4-(2,2-dimethoxyethyl)phenyl)methanol 
• 124791-75-9 methyl 4-(2,2-dimethoxyethyl)benzoate 
• 140639-94-7 2-(3'-hydroxymethyl)phenyl-1,3-dioxolane 

Relevant articles and documents

CINNOLINE DERIVATIVES USEFUL AS CB-1 RECEPTOR INVERSE AGONISTS

The present invention is directed to cinnoline derivatives of formula (I) pharmaceutical compositions containing them and their use in the treatment of disorders and conditions mediated by the CB-1 receptor; more particularly, use in the treatment of disorders and conditions responsive to inverse agonism of the CB-1 receptor. More particularly, the compounds of the present invention are useful in the treatment of metabolic disorders.

COMPOUNDS HAVING MUSCARINIC RECEPTOR ANTAGONIST AND BETA2 ADRENERGIC RECEPTOR AGONIST ACTIVITY

Compounds of formula (I) described herein act both as muscarinic receptor antagonists and beta2 adrenergic receptor agonists and are useful for the prevention and/or treatment of broncho-obstructive or inflammatory diseases.

Rhodium-catalyzed anti-Markovnikov intermolecular hydroalkoxylation of terminal acetylenes

We report here the first transition-metal-catalyzed anti-Markovnikov intermolecular hydroalkoxylation of terminal acetylenes to give enol ethers in high yields without using bases. Arylacetylenes as well as alkenyl- and alkylacetylenes were coupled with aliphatic alcohols, and the products were obtained with high Z selectivity in most cases. Effective catalysts were 8-quinolinolato rhodium complexes, which are structurally simple but have been relatively unexplored as catalysts.