55907-61-4 Usage
Uses
Used in Laboratory Applications:
2,4-Dinitrophenylhydrazine hydrochloride is used as a detection reagent for the identification and analysis of carbonyl compounds, such as aldehydes and ketones. It forms yellow to orange precipitates, which aid in the qualitative assessment of these compounds.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 2,4-Dinitrophenylhydrazine hydrochloride is utilized as a synthetic intermediate for the production of various organic compounds and pharmaceuticals. Its reactivity and versatility make it a valuable component in the synthesis process.
Used in Industrial Applications:
2,4-Dinitrophenylhydrazine hydrochloride is employed in various industrial processes, where its reagent properties are harnessed for the detection and analysis of carbonyl compounds. Its application in these settings contributes to the quality control and assurance of chemical products.
Safety Precautions:
Due to the explosive and toxic nature of 2,4-Dinitrophenylhydrazine hydrochloride, it is crucial to follow proper safety protocols when handling and storing 2,4-DINITROPHENYLHYDRAZINE HYDROCHLORIDE. This includes wearing appropriate personal protective equipment, working in well-ventilated areas, and adhering to specific storage guidelines to minimize the risk of accidents and exposure.
Check Digit Verification of cas no
The CAS Registry Mumber 55907-61-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,9,0 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55907-61:
(7*5)+(6*5)+(5*9)+(4*0)+(3*7)+(2*6)+(1*1)=144
144 % 10 = 4
So 55907-61-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N4O4.ClH/c7-8-5-2-1-4(9(11)12)3-6(5)10(13)14;/h1-3,8H,7H2;1H
55907-61-4Relevant academic research and scientific papers
Design, synthesis, crystal structures, and insecticidal activities of eight-membered azabridge neonicotinoid analogues
Xu, Renbo,Xia, Rui,Luo, Ming,Xu, Xiaoyong,Cheng, Jiagao,Shao, Xusheng,Li, Zhong
, p. 381 - 390 (2014/02/14)
Three series of novel azabridge neonicotinoid analogues were designed and synthesized, which were constructed by starting material A, glutaraldehyde, and primary amine hydrochlorides (aliphatic amines, phenylhydrazines, and anilines). Most of the eight-membered azabridge compounds presented higher insecticidal activities than oxabridged compound B against cowpea aphid (Aphis craccivora) and brown planthopper (Nilaparvata lugens). Compared with imidacloprid, some azabridged compounds exhibited excellent insecticidal activity against brown planthopper. The crystal structures and bioassay indicated that changing bridge atoms from O to N could lead to entirely different conformations, which might be the important influential factor of the bioactivities.
