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(1R,2R,7S,8S)-4-p-Tolyl-5-oxa-3-aza-tricyclo[6.2.1.0^2,7]undec-3-ene is a complex organic compound with a unique molecular structure. It is a tricyclic molecule, which means it consists of three interconnected rings. The compound features a 5-oxa-3-aza core, indicating the presence of an oxygen atom and a nitrogen atom in the ring structure. The p-tolyl group, a substituted benzene ring with a methyl group, is attached to the molecule, contributing to its specific properties. (1R,2R,7S,8S)-4-p-Tolyl-5-oxa-3-aza-tricyclo[6.2.1.02,7]undec-3-ene is characterized by its chiral centers, with four stereocenters (1R, 2R, 7S, 8S), which determine its stereochemistry and potential biological activity. The specific arrangement of these centers and the overall structure of the molecule can influence its reactivity, stability, and potential applications in various fields, such as pharmaceuticals or materials science.

87768-86-3

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87768-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87768-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,6 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 87768-86:
(7*8)+(6*7)+(5*7)+(4*6)+(3*8)+(2*8)+(1*6)=203
203 % 10 = 3
So 87768-86-3 is a valid CAS Registry Number.

87768-86-3Relevant academic research and scientific papers

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

Stajer, Geza,Szabo, Angela E.,Fueloep, Ferenc,Bernath, Gabor,Sohar, Pal

, p. 1373 - 1376 (2007/10/02)

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

Stajer,Szabo,Fulop,et al.

, p. 1181 - 1185 (2007/10/02)

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

Sohar, P.,Stajer, G.,Bernath, G.

, p. 512 - 519 (2007/10/02)

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

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