65655-78-9

Basic information

• Product Name: ethyl 2,2-dibromo-1-phenylcyclopropanecarboxylate
• Synonyms: ethyl 2,2-dibromo-1-phenylcyclopropanecarboxylate
• CAS NO: 65655-78-9
• Molecular Weight: 348.034
• Mol File: 65655-78-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl 2,2-dibromo-1-phenylcyclopropanecarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2,2-dibromo-1-phenylcyclopropanecarboxylate(65655-78-9)
• EPA Substance Registry System: ethyl 2,2-dibromo-1-phenylcyclopropanecarboxylate(65655-78-9)

Safety Data

• Hazardous Substances Data: 65655-78-9(Hazardous Substances Data)

Upstream product

• 75-25-2 Bromoform 
• 22286-82-4 2-phenyl-acrylic acid ethyl ester 

Downstream Products

• 6120-95-2 1-phenyl-1-cyclopropane carboxylic acid 
• 104173-58-2 C₁₁H₁₁⁽²⁾HO₂ 
• 104173-57-1 C₁₁H₁₁⁽²⁾HO₂ 
• 69368-98-5 2-Brom-1-phenylcyclopropyl-methanol 
• 66078-16-8 (E)-2-Brom-1-phenylcyclopropancarbonsaeureaethylester 
• 66078-17-9 (Z)-2-Brom-1-phenylcyclopropancarbonsaeureaethylester 
• 87328-17-4 ethyl 1-phenyl-1-cyclopropanecarboxylate 
• 67074-45-7 2,2-dibromo-1-phenylcyclopropylmethanol 

Relevant articles and documents

Deamination Reactions, 45. Decomposition of 1-Arylcyclopropanediazonium Ions

1-Arylcyclopropanediazonium ions have been generated by alkaline cleavage of the analogous nitrosocarbamates in methanol.With increasing ?-donor capacity of the aryl groups, retention of the three-membered ring was enhanced while the stereoselectivity (as probed with the aid of 2-D labels) was diminished or entirely lost (4-methoxyphenyl).Where applicable, the stereoselectivity of ring opening is inferior to that of nucleophilic displacement.The data may be interpreted in terms of competing reactions (ks, kc, kΔ) of the cyclopropanediazonium ions.