881919-79-5

Basic information

• Product Name: 1-bromo-1-(3-ethoxy-4-methoxyphenyl)ethene
• Synonyms: 1-bromo-1-(3-ethoxy-4-methoxyphenyl)ethene
• CAS NO: 881919-79-5
• Molecular Weight: 257.127
• Mol File: 881919-79-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-bromo-1-(3-ethoxy-4-methoxyphenyl)ethene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-1-(3-ethoxy-4-methoxyphenyl)ethene(881919-79-5)
• EPA Substance Registry System: 1-bromo-1-(3-ethoxy-4-methoxyphenyl)ethene(881919-79-5)

Safety Data

• Hazardous Substances Data: 881919-79-5(Hazardous Substances Data)

Upstream product

• 1131-62-0 1-(3,4-dimethoxyphenyl)ethanone 
• 1131-52-8 3-ethoxy-4-methoxybenzaldehyde 
• 6100-74-9 3-hydroxy-4-methoxyacetophenone 
• 881919-85-3 1,1-dibromo-2-(3-ethoxy-4-methoxyphenyl)ethene 
• 31526-71-3 3-ethoxy-4-methoxy-acetophenone 
• 881919-82-0 3-ethoxy-4-methoxyphenylacetylene 

Downstream Products

• 882030-12-8 (3R,4R)-3-(3-ethoxy-4-methoxy-phenyl)-tetrahydro-thiopyran-4-ylamine hydrochloride 
• 882030-13-9 [(3R,4R)-3-(3-ethoxy-4-methoxy-phenyl)-tetrahydro-thiopyran-4-yl]-((R)-1-phenyl-ethyl)-amine hydrochloride 
• 881919-73-9 2-(3-ethoxy-4-methoxyphenyl)-1,4-pentadien-3-ol 
• 907997-21-1 (E)-4-(3-ethoxy-4-methoxyphenyl)-1-phenyl-1,4-pentadien-3-ol 
• 907997-11-9 (E)-4-(3-ethoxy-4-methoxyphenyl)-1-phenyl-1,4-pentadien-3-one 
• 882030-14-0 3-(3-ethoxy-4-methoxyphenyl)tetrahydrothiopyran-4-one 
• 907997-18-6 3-(3-ethoxy-4-methoxyphenyl)tetrahydropyran-4-one 
• 881919-71-7 2-(3-ethoxy-4-methoxyphenyl)-1,4-pentadien-3-one 

Relevant articles and documents

Novel 3-Thia-10-Aza-Phenanthrene Derivatives

The compounds of formula I in which A, R1, R2 and R3 have the meanings as given in the description, are novel effective PDE4 inhibitors.

Synthesis of tetrahydropyran-4-ones and thiopyran-4-ones from donor-substituted α-bromostyrene derivatives

Tetrahydropyran-4-one and tetrahydrothiopyran-4-one derivatives with a 3-aryl substituent were synthesized by double-conjugate addition of water or H2S to divinyl ketones. These starting materials were prepared in two steps by conversion of lit