16192-27-1 Usage
General Description
1,2-dimethyl-2,3-dihydro-1H-indazole is a chemical compound with the molecular formula C10H14N2. It is a bicyclic organic compound belonging to the indazole class. 1,2-dimethyl-2,3-dihydro-1H-indazole is derived from indazole by the addition of two methyl groups at the 1 and 2 positions, and a dihydro group at the 2 and 3 positions of the indazole ring. It is a colorless liquid with a boiling point of 215-217°C and is sparingly soluble in water. 1,2-dimethyl-2,3-dihydro-1H-indazole is primarily used as a building block in the synthesis of pharmaceuticals and agricultural chemicals. It is also a precursor to various dyes and pigments, and is utilized in research and development for its versatile chemical reactivity. Due to its potential toxicological effects, proper handling and safety precautions are recommended when working with this compound.
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.
