22107-29-5 Usage
General Description
2-[1-(3-nitrophenyl)ethylidene]hydrazinecarboxamide is a chemical compound with the molecular formula C9H10N4O3. It is not found naturally in the environment, but can be synthesized in a laboratory setting. 2-[1-(3-nitrophenyl)ethylidene]hydrazinecarboxamide is a hydrazine derivative and is commonly used in pharmaceutical research and drug development as a potential candidate for the treatment of various diseases. It is also a key ingredient in the production of certain dyes and pigments due to its vibrant color properties. However, it is important to handle 2-[1-(3-nitrophenyl)ethylidene]hydrazinecarboxamide with caution as it may pose potential health hazards if not used properly. Additionally, it is important to adhere to proper safety protocols when working with 2-[1-(3-nitrophenyl)ethylidene]hydrazinecarboxamide in order to prevent any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 22107-29-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,0 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22107-29:
(7*2)+(6*2)+(5*1)+(4*0)+(3*7)+(2*2)+(1*9)=65
65 % 10 = 5
So 22107-29-5 is a valid CAS Registry Number.
22107-29-5Relevant academic research and scientific papers
Preparation of 2-Arylethynylselanylacetonitriles from 4-Aryl-1,2,3-selenadiazoles
O'Connor,Sachinvala,Ganjian
, p. 1167 - 1169 (2015/08/06)
Base decomposition of 4-(substituted phenyl)-1,2,3-selenadiazoles at room temperature resulted in 2-(substituted phenyl)-ethynylselenolate anions, which were immediately reacted with bromoacetonitrile to give a series of 2-(substituted phenyl)ethynylselan
Synthesis of 3-substituted arylpyrazole-4-carboxylic acids
Lebedev,Lebedeva,Sheludyakov,Kovaleva,Ustinova,Kozhevnikov
, p. 782 - 789 (2007/10/03)
A method was suggested for preparing previously unknown 3-aryl-substituted pyrazole-4-carboxylic acids, involving Vilsmeier formylation of semicarbazones of 26 available mono- and disubstituted acetophenones and 2-acetylthiophene followed by oxidation of
