96693-31-1 Usage
Chemical structure
A diphosphete derivative with a lithium salt.
Use
As a reagent for the formation of C-P bonds and functionalization of organic compounds.
Potential applications
Building block for constructing complex organic molecules, pharmaceutical and agrochemical industries.
Research value
Unique structure and reactivity for chemical and material science research.
Safety precautions
Proper handling and safety measures should be taken to prevent potential hazards.
Please note that this is a summary based on the provided material, and further research may be needed for a more comprehensive understanding of the compound.
Check Digit Verification of cas no
The CAS Registry Mumber 96693-31-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,6,9 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 96693-31:
(7*9)+(6*6)+(5*6)+(4*9)+(3*3)+(2*3)+(1*1)=181
181 % 10 = 1
So 96693-31-1 is a valid CAS Registry Number.
96693-31-1Relevant articles and documents
Exocyclic P-C vs. Endocyclic P-P Bond Cleavage in 1,2-Diphosphetes. A Competition between Cyclic Delocalization and Cyclic Strain Controlled by the Substitution Pattern
Charrier, Claude,Mathey, Francois,Robert, Francis,Jeannin, Yves
, p. 1707 - 1708 (1984)
Attack by lithium on 1,2-diphenyl-3,4-di-R-substituted-1,2-diphosphetes takes place on the endocyclic P-P bond when R=Ph whereas it takes place on the exocyclic P-Ph bond when R=tBu; in this latter case, a 1,2-diphosphet-1-yl anion is obtained which is probably stabilized by cyclic delocalization.
