131179-10-7

Basic information

• Product Name: 7-Azabicyclo[2.2.1]hept-2-ene-7-carboxylicacid,methylester,anti-(9CI)
• Synonyms: 7-Azabicyclo[2.2.1]hept-2-ene-7-carboxylicacid,methylester,anti-(9CI)
• CAS NO: 131179-10-7
• Molecular Formula: C₈H₁₁NO₂
• Molecular Weight: 153.18
• Product Categories: CARBOXYLICESTER
• Mol File: 131179-10-7.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 219.4±29.0 °C(Predicted)
• Appearance: /
• Density: 1.204±0.06 g/cm3(Predicted)
• PKA: -1.65±0.20(Predicted)
• CAS DataBase Reference: 7-Azabicyclo[2.2.1]hept-2-ene-7-carboxylicacid,methylester,anti-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 7-Azabicyclo[2.2.1]hept-2-ene-7-carboxylicacid,methylester,anti-(9CI)(131179-10-7)
• EPA Substance Registry System: 7-Azabicyclo[2.2.1]hept-2-ene-7-carboxylicacid,methylester,anti-(9CI)(131179-10-7)

Safety Data

• Hazardous Substances Data: 131179-10-7(Hazardous Substances Data)

Upstream product

• 213745-87-0 2-(Toluene-4-sulfonyl)-3-trimethylsilanyl-7-aza-bicyclo[2.2.1]hept-2-ene-7-carboxylic acid methyl ester 
• 83060-74-6 7-methoxycarbonyl-2-p-toluenesulfonyl-7-azanorbornadiene 
• 4277-63-8 methyl 1H-pyrrole-1-carboxylate 
• 5535-48-8 PVS 
• 131193-46-9 2-(Toluene-4-sulfonyl)-7-aza-bicyclo[2.2.1]hept-2-ene-7-carboxylic acid methyl ester 

Downstream Products

• 55590-24-4 7-Azabicyclo[2.2.1]-hept-2-ene 
• 155322-26-2 dechloro-epibatidine 

Relevant articles and documents

The synthesis of epiboxidine and related analogues as potential pharmacological agents

Methyl epiboxidine-N-carboxylate (8) was synthesized from 7 under reductive Heck conditions (Scheme 2). The C-C coupling of the new epiboxidine analog 9 with aryl and heteroaryl halides gave by hydroarylation C-aryl, N-(3-methylisoxazol-5-yl)-substituted

2-(Het)aryl-substituted 7-azabicyclo[2.2.1]heptane systems

Epibatidine (1) is a recently discovered trace alkaloid found in the skin of a Latin-Amencan poisonous frog. Its remarkably high analgetic activity is accompanied by high toxicity. Therefore, in order to tune its biological activity, a convergent and effi

A Total Synthesis of (+/-)-Epibatidine

A total synthesis of the potent non-opiate analgesic alcaloid epibatidine is described, in which the key step is reductive palladium-catalysed Heck-type coupling.The synthesis is concise (two steps from known compounds), highly convergent, and completely sttereoselective for the desired exo-isomer. - Key Words: Epibatidine, Analgesic, Alkaloid, Palladium-catalysed Coupling