239077-92-0 Usage
Explanation
The compound's name provides information about its structure and stereochemistry.
2. Hexahydro-derivative
Explanation
The compound is a derivative of 1,4-Ethano-5,8-methanonaphthalene-10,11-dione with six hydrogen atoms added to its structure.
Explanation
The stereochemistry of the compound is defined by the arrangement of its atoms in three-dimensional space, which can influence its biological activities and interactions.
4. Chemical Research and Synthesis
Explanation
Due to its complex structure, the compound is likely to be used in chemical research and synthesis for further exploration of its properties and potential applications.
5. Biological Activities or Interactions
Explanation
The stereochemistry of the compound suggests that it may have specific biological activities or interactions, which would need to be further studied and researched.
6. Further Research Required
Explanation
The exact uses and properties of this chemical would need to be further studied and researched to fully understand its potential applications and effects.
Stereochemistry
(1R,4S,4aR,5R,8S,8aS)-rel-
Check Digit Verification of cas no
The CAS Registry Mumber 239077-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,9,0,7 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 239077-92:
(8*2)+(7*3)+(6*9)+(5*0)+(4*7)+(3*7)+(2*9)+(1*2)=160
160 % 10 = 0
So 239077-92-0 is a valid CAS Registry Number.
239077-92-0Relevant articles and documents
Direct formation of α-dione blocks from o-benzoquinone cycloadditions and their value in the synthesis of fused quinoxalines, 1,10-phenanthrolines and pteridines
Warrener, Ronald N.,Johnston, Martin R.,Schultz, Austin C.,Golic, Mirta,Houghton, Mark A.,Gunter, Maxwell J.
, p. 590 - 592 (1998)
o-Benzoquinone reacts with norbornadiene to yield a mixture of exo and endo stereoisomeric bridged α-diones which are condensed with vic-diamines (o-phenylenediamines, 5,6-diamino uracil or 5,6-diaminophenanthroline) to produce the corresponding heterocyclic fused-norbornenes; other rod or angled molrac α-dione blocks and heterocycles derived therefrom are described which open new avenues for macrostructure development via block coupling protocols.
