101064-79-3 Usage
Family
Quinoline family
Function
Bioluminescent substrate
Applications
Chemiluminescent marker in biochemical and biotechnological applications
Role in Research
Essential in studying protein-protein interactions, gene expression, and enzyme activity
Chemical Structure
Three methyl-but-2-enyl groups attached to the quinoline core
Light Emission
Efficient light emission when oxidized by luciferase enzymes
Utilization
Widely used in research and diagnostic fields
Check Digit Verification of cas no
The CAS Registry Mumber 101064-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,6 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 101064-79:
(8*1)+(7*0)+(6*1)+(5*0)+(4*6)+(3*4)+(2*7)+(1*9)=73
73 % 10 = 3
So 101064-79-3 is a valid CAS Registry Number.
101064-79-3Relevant articles and documents
A REVERSIBLE CLAISEN REARRANGEMENT OF 3-(3,3-DIMETHYLALLYL)-4-(3,3-DIMETHYLALLYLOXY)QUINOLIN-2-ONE; SYNTHESIS OF BUCHAPSINE AND LOSS OF ITS 1,1-DIMETHYLALLYL GROUP
Grundon, Michael F.,Ramachandran, V. N.
, p. 4253 - 4256 (1985)
Reversible Claisen rearrangement of 3-(3,3-dimethylallyl)-4-(3,3-dimethylallyloxy)quinolin-2-one (5) furnished the alkaloid, buchapsine (6), which readily lost the 1,1-dimethylallyl group; a mechanism for the cleavage reaction is proposed.
