78283-22-4 Usage
Uses
Used in Organic Synthesis:
2,6-Dinitrophenyl acetaldehyde is used as a reagent in the preparation of various organic compounds, facilitating the synthesis of a range of chemical products. Its unique properties make it a valuable component in the creation of new molecules and materials.
Used in Chemical Research:
In the realm of chemical research, 2,6-Dinitrophenyl acetaldehyde serves as a starting material for the synthesis of other chemicals, contributing to the advancement of scientific knowledge and the development of novel chemical processes.
Used in Detection and Analysis of Aldehydes and Ketones:
2,6-Dinitrophenyl acetaldehyde is utilized in the detection and analysis of aldehydes and ketones through the formation of colored derivatives. This application is crucial for identifying and quantifying these types of compounds in various chemical and industrial processes.
Used in Safety Protocols:
Due to its explosive nature and potential health hazards, 2,6-Dinitrophenyl acetaldehyde is also used as a subject of study in the development of safety protocols for handling and storage, ensuring the protection of researchers and the environment from potential risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 78283-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,2,8 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78283-22:
(7*7)+(6*8)+(5*2)+(4*8)+(3*3)+(2*2)+(1*2)=154
154 % 10 = 4
So 78283-22-4 is a valid CAS Registry Number.
78283-22-4Relevant academic research and scientific papers
Synthetic Studies in the Indole Series. Preparation of the Unique Antibiotic Alkaloid Chuangxinmycin by a Nitro Group Displacement Reaction
Kozikowski, Alan P.,Greco, Michael N.,Springer, James P.
, p. 7622 - 7626 (2007/10/02)
The total synthesis of the unique sulfur-containing antibiotic indole alkaloid chuangxinmycin is described.This compound, first isolated by Chinese chemists at the Institute of Materia Medica, was assembled from 2,6-dinitrotoluene by a scheme that combine
