78648-35-8 Usage
Classification
piperidine carboxylic acid derivative This indicates the functional groups present in the molecule and its chemical structure.
Use
pharmaceutical and research industries This indicates the general applications of the compound.
Potential therapeutic agent
treatment of neurological and psychiatric disorders This indicates the specific potential medical uses of the compound.
Building block in organic synthesis
useful precursor for the synthesis of various other compounds This indicates the specific chemical uses of the compound.
Handling precautions
should be handled with care due to potential biological activity This indicates the potential risks and hazards associated with the compound.
Check Digit Verification of cas no
The CAS Registry Mumber 78648-35-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,4 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 78648-35:
(7*7)+(6*8)+(5*6)+(4*4)+(3*8)+(2*3)+(1*5)=178
178 % 10 = 8
So 78648-35-8 is a valid CAS Registry Number.
78648-35-8Relevant articles and documents
Parallel synthesis and spectroscopic analysis of a collection of heterocycles based on the diazabenz[e]aceanthrylene core structure
Jones, Alan M.,Lebl, Tomas,Patterson, Stephen,van Mourik, Tanja,Früchtl, Herbert A.,Philp, Douglas,Slawin, Alexandra M.Z.,Westwood, Nicholas J.
supporting information; experimental part, p. 563 - 578 (2009/04/06)
A practical strategy for the synthesis of diazabenz[e]aceanthrylene-based heterocycles is reported. The key step in this approach is a microwave-assisted condensation and cyclisation reaction between an anthranilic acid derivative and a 2′-carbomethoxy substituted N-aryl lactam. The scope of the reaction has been explored as a function of both the nature and position of substituents in both components and variations in lactam ring size. Interesting structural and spectroscopic variations observed across the compound collection are described and explored using NMR, X-ray crystallography and computational techniques.
Tricyclic benzoxazinones
Moehrle,Busch
, p. 524 - 531 (2007/10/02)
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