87768-87-4

Basic information

• Product Name: (1R,2R,7S,8S)-4-(4-Chloro-phenyl)-5-oxa-3-aza-tricyclo[6.2.1.0^2,7]undec-3-ene
• CAS NO: 87768-87-4
• Molecular Weight: 261.751
• Mol File: 87768-87-4.mol

Chemical Properties

• CAS DataBase Reference: (1R,2R,7S,8S)-4-(4-Chloro-phenyl)-5-oxa-3-aza-tricyclo[6.2.1.0^2,7]undec-3-ene(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R,7S,8S)-4-(4-Chloro-phenyl)-5-oxa-3-aza-tricyclo[6.2.1.0^2,7]undec-3-ene(87768-87-4)
• EPA Substance Registry System: (1R,2R,7S,8S)-4-(4-Chloro-phenyl)-5-oxa-3-aza-tricyclo[6.2.1.0^2,7]undec-3-ene(87768-87-4)

Safety Data

• Hazardous Substances Data: 87768-87-4(Hazardous Substances Data)

Upstream product

• 78365-98-7 3-endo-Hydroxymethylbicyclo<2.2.1>heptyl-2-endo-amine 
• 827-72-5 4-chlorobenzimidic acid ethyl ester 
• 95630-74-3 Ethyl 3-endo-Aminobicyclo<2.2.1>hept-5-ene-2-endo-carboxylate Hydrochloride 
• 78365-98-7 rac-((1R,2S,3R,4S)-3-aminobicyclo[2.2.1]heptan-2- yl)methanol 
• 88330-32-9 2,3-diexo-3-aminobicyclo[2.2.1]heptane-2-carboxylic acid 
• 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 

Downstream Products

• 112673-28-6 C₂₈H₂₆ClN₃O 
• 3457-46-3 4,4'-dichlorobenzil 
• 115879-38-4 N-(4-Chlorbenzyl)-3-(hydroxymethyl)norbornyl-2-amin 
• 136004-62-1 10at-p-chlorophenyl-5,8-methano-3-methyl-4ar,5t,6,7,8t,8ac-hexahydro-9H-<1,2,4>oxadiazolo<4,5-y>benzoxazine 
• 112673-28-6 2-p-chlorophenyl-5,8-methano-1,2R*,4aR*,5,6,7,8,8aS*-octahydro-4H-3,1-benzoxazino<2.1-c>-2,5-diphenyl-2H-1,2,4-triazoline 
• 115879-39-5 α,α'-Bis<3-(hydroxymethyl)norbornyl-2-amino>-4,4'-dichlorbibenzyl 
• 136004-62-1 10ac-p-chlorophenyl-5,8-methano-3-methyl-4ar,5c,6,7,8c,8ac-hexahydro-9H-<1,2,4>oxadiazolo<4,5-a>benzoxazine 

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