16192-27-1 Usage
Bicyclic organic compound
Yes
Belongs to the indazole class
Yes
Derived from indazole
Yes
Addition of two methyl groups
At the 1 and 2 positions
Addition of a dihydro group
At the 2 and 3 positions of the indazole ring
Physical state
Colorless liquid
Boiling point
215-217°C
Solubility in water
Sparingly soluble
Primary use
Building block in the synthesis of pharmaceuticals and agricultural chemicals
Precursor to
Various dyes and pigments
Utilized in
Research and development for versatile chemical reactivity
Toxicological effects
Potential, proper handling and safety precautions recommended
Check Digit Verification of cas no
The CAS Registry Mumber 16192-27-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,9 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16192-27:
(7*1)+(6*6)+(5*1)+(4*9)+(3*2)+(2*2)+(1*7)=101
101 % 10 = 1
So 16192-27-1 is a valid CAS Registry Number.
16192-27-1Relevant articles and documents
Elemental step thermodynamics of various analogues of indazolium alkaloids to obtaining hydride in acetonitrile
Lei, Nan-Ping,Fu, Yan-Hua,Zhu, Xiao-Qing
, p. 11472 - 11485 (2015/12/04)
A series of analogues of indazolium alkaloids were designed and synthesized. The thermodynamic driving forces of the 6 elemental steps for the analogues of indazolium alkaloids to obtain hydride in acetonitrile were determined using an isothermal titration calorimeter (ITC) and electrochemical methods, respectively. The effects of molecular structure and substituents on the thermodynamic driving forces of the 6 steps were examined. Meanwhile, the oxidation mechanism of NADH coenzyme by indazolium alkaloids was examined using the chemical mimic method. The result shows that the oxidation of NADH coenzyme by indazolium alkaloids in vivo takes place by one-step concerted hydride transfer mechanism.