69718-72-5 Usage
General Description
10-AZA-TRICYCLO[6.3.1.0]DODECA-2,4,6-TRIENE TOSYLATE is a compound that is derived from tricyclic organic chemicals. It is tosylate, which means it contains a tosyl group, a functional group that is often used in organic synthesis. The compound has a tricyclic structure with 12 carbon atoms, and contains a nitrogen atom within the ring system. This chemical may have potential applications in medicinal chemistry, as tricyclic compounds are commonly used as the basis for antidepressant and antipsychotic drugs. Additionally, the tosylate group can make the compound more reactive, which may be useful in synthetic chemistry for creating new molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 69718-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,1 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69718-72:
(7*6)+(6*9)+(5*7)+(4*1)+(3*8)+(2*7)+(1*2)=175
175 % 10 = 5
So 69718-72-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H13N/c1-2-4-11-9-5-8(6-12-7-9)10(11)3-1/h1-4,8-9,12H,5-7H2
69718-72-5Relevant articles and documents
Mazzocchi,Stahly
, p. 455 (1979)
Synthesis of 2,3,4,5-tetrahydro-1,5-methano-1H-3-benzazepine via oxidative cleavage and reductive amination strategies
Brooks, Paige R.,Caron, Stephane,Coe, Jotham W.,Ng, Karl K.,Singer, Robert A.,Vazquez, Enrique,Vetelino, Michael G.,Watson Jr., Harry H.,Whritenour, David C.,Wirtz, Michael C.
, p. 1755 - 1758 (2007/10/03)
Preparations of 2,3,4,5-tetrahydro-1,5-methano-1H-3-benzazepine (5) from benzonorbornadiene (1) by oxidative cleavage and reductive amination sequences were investigated. Osmium-mediated dihydroxylation of 1 followed by NaIO 4 cleavage, reductive amination and debenzylation provides 5 in 64-73% yield overall in three operations. A tandem ozonolysis-reductive amination procedure gives 5 as the tosylate salt from benzonorbornadiene with no isolation of intermediates in 28% yield.
