87768-88-5

Basic information

• Product Name: (1S,2R,7S,8R)-4-(3-Chloro-phenyl)-5-oxa-3-aza-tricyclo[6.2.1.0^2,7]undec-3-ene
• CAS NO: 87768-88-5
• Molecular Weight: 261.751
• Mol File: 87768-88-5.mol

Chemical Properties

• CAS DataBase Reference: (1S,2R,7S,8R)-4-(3-Chloro-phenyl)-5-oxa-3-aza-tricyclo[6.2.1.0^2,7]undec-3-ene(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2R,7S,8R)-4-(3-Chloro-phenyl)-5-oxa-3-aza-tricyclo[6.2.1.0^2,7]undec-3-ene(87768-88-5)
• EPA Substance Registry System: (1S,2R,7S,8R)-4-(3-Chloro-phenyl)-5-oxa-3-aza-tricyclo[6.2.1.0^2,7]undec-3-ene(87768-88-5)

Safety Data

• Hazardous Substances Data: 87768-88-5(Hazardous Substances Data)

Upstream product

• 88330-32-9 2,3-diexo-3-aminobicyclo[2.2.1]heptane-2-carboxylic acid 
• 827-64-5 ethyl 3-chlorobenzenecarboximidate hydrochloride 
• 78365-98-7 rac-((1R,2S,3R,4S)-3-aminobicyclo[2.2.1]heptan-2- yl)methanol 
• 95630-75-4 Ethyl 3-endo-Aminobicyclo<2.2.1>heptane-2-endo-carboxylate Hydrochloride 
• 95630-77-6 Ethyl 3-endo-Aminobicyclo<2.2.1>heptane-2-endo-carboxylate 
• 53623-52-2 3-endo-Aminobicyclo<2.2.1>hept-5-ene-2-endo-carboxylic Acid 
• 76198-36-2 3-exo-Aminobicyclo<2.2.1>heptane-2-exo-carboxylic Acid 
• 95630-74-3 Ethyl 3-endo-Aminobicyclo<2.2.1>hept-5-ene-2-endo-carboxylate Hydrochloride 
• 78365-98-7 3-endo-Hydroxymethylbicyclo<2.2.1>heptyl-2-endo-amine 

Relevant articles and documents

Stereochemical Studies. 81 . Saturated Heterocycles. 69 . Preparation of Methylene-bridged 3,1-Benzoxazines, 3,1-Benzoxazin-2-ones and 3,1-Benzoxazine-2-thiones

3-exo-Aminobicyclohept-5-ene-2-exo-carboxylic acid and ethyl 3-endo-aminobicycloheptane-2-endo-carboxylate (6) were reduced with lithium aluminum hydride to the corresponding bicyclic aminoalcohols 3 and 4.These and the saturated endo-endo a

Stereochemical studies, 58, saturated heterocycles, 39 [1]. Preparation and steric structures of dihydro-1,3-oxazines, 1,3-oxazin-2-ones and 1,3-oxazine-2-thiones fused with norbornane and norbornene

3-endo-Aminobicyclo[2.2.1]hept-5-ene-2-endo-carboxylic acid(1), prepared from endo-norborn-5-ene-2,3-dicarboxylic acid anhydride, and the analogous saturated cis-exo-amino acid (3) were reduced with lithium aluminum hydride to the aminoalcohols 2 and 4; t

Configuration and NMR Study of Tricyclic Oxazines Fused to a Norbornene or Norbornane Skeleton

Tricyclic oxazines fused with norbornene or norbornane were synthesized for pharmacological and stereochemical purposes.Analogous oxazin-2-ones and 2-thiones were also obtained.The diendo or diexo anellation of the hetero ring to the norbornene or norborn