2122-01-2 Usage
Uses
Used in Organic Synthesis:
1-(hex-3-enylidene)-2-(2,4-dinitrophenyl)hydrazine is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of complex organic molecules.
Used in Analytical Chemistry:
In analytical chemistry, 1-(hex-3-enylidene)-2-(2,4-dinitrophenyl)hydrazine serves as a reagent, facilitating the detection, identification, and quantification of specific compounds through its characteristic reactions.
Used in Metal Complex Chemistry:
1-(hex-3-enylidene)-2-(2,4-dinitrophenyl)hydrazine is used as a potential ligand in metal complex chemistry, where it can form coordination compounds with certain metals, offering new avenues for research and applications in materials science.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(hex-3-enylidene)-2-(2,4-dinitrophenyl)hydrazine is studied for its potential biological activities, which may lead to the development of new drugs or therapeutic agents.
Used in Agrochemical Development:
Similarly, in agrochemicals, 1-(hex-3-enylidene)-2-(2,4-dinitrophenyl)hydrazine is being investigated for its possible applications, potentially contributing to the development of new pesticides or other agricultural chemicals.
It is crucial to handle 1-(hex-3-enylidene)-2-(2,4-dinitrophenyl)hydrazine with caution due to its potential hazards, ensuring safety for both health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 2122-01-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,2 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2122-01:
(6*2)+(5*1)+(4*2)+(3*2)+(2*0)+(1*1)=32
32 % 10 = 2
So 2122-01-2 is a valid CAS Registry Number.
2122-01-2Relevant academic research and scientific papers
Selective reduction of carboxylic acids to aldehydes catalyzed by B(C 6F5)3
Bezier, David,Park, Sehoon,Brookhart, Maurice
supporting information, p. 496 - 499 (2013/03/29)
B(C6F5)3 efficiently catalyzes hydrosilylation of aliphatic and aromatic carboxylic acids to produce disilyl acetals under mild conditions. Catalyst loadings can be as low as 0.05 mol %, and bulky tertiary silanes are favored to give selectively the acetals. Acidic workup of the disilyl acetals results in the formation of aldehydes in good to excellent yields.
