50610-82-7 Usage
Type of compound
Heterocyclic organic compound
Structure
Quinoline ring system with a phenylmethyl group attached at the 2-position
Field of use
Medicinal chemistry and drug development
Potential properties
Pharmacological properties
Role in neurotransmission
Investigated for its potential involvement in neurobiological functions
Importance
Unique structure and potential biological activities for further exploration and study
Check Digit Verification of cas no
The CAS Registry Mumber 50610-82-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,1 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 50610-82:
(7*5)+(6*0)+(5*6)+(4*1)+(3*0)+(2*8)+(1*2)=87
87 % 10 = 7
So 50610-82-7 is a valid CAS Registry Number.
50610-82-7Relevant articles and documents
Efficient entry into 2-substituted tetrahydroquinoline systems through alkylative ring expansion: Stereoselective formal synthesis of (±)-martinellic acid
Ueda, Masafumi,Kawai, Sayuri,Hayashi, Masataka,Naito, Takeaki,Miyata, Okiko
experimental part, p. 914 - 921 (2010/06/16)
(Chemical Equation Presented) A new efficient synthesis of 2-substituted tetrahydroquinolines has been achieved by the domino reaction of N-indanyl(methoxy)amines, which consists of three types of reactions: elimination of an alcohol, the rearrangement of an aryl group, and the addition of an organolithium or magnesium reagent. The synthetic utility of this approach is demonstrated by the stereoselective formal synthesis of (±)- martinellic acid.
2-Substituted 1,2,3,4-tetrahydroquinolines from quinoline
Goldstein,Dambek
, p. 221 - 222 (2007/10/02)
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