2684-60-8 Usage
Uses
Used in Organic Synthesis:
2-Diazopropane is used as a diazo compound in organic synthesis for the introduction of a diazo group into organic molecules. This property makes it a valuable reagent in the creation of a wide range of organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Diazopropane is used as a reagent in the preparation of various pharmaceutical compounds. Its ability to form new carbon-carbon bonds through the generation of carbene intermediates contributes to the development of novel drug molecules.
Used in Dye Production:
2-Diazopropane is utilized in the production of dyes due to its role as a reagent in the synthesis of dye molecules. Its chemical properties allow for the creation of a variety of dyes with different characteristics.
Used in Chemical Reactions:
2-Diazopropane is used in various chemical reactions, including decomposition under heat or light to form nitrogen gas and a carbene intermediate. This ability to generate reactive intermediates makes it a useful compound in the formation of new carbon-carbon bonds and the synthesis of complex organic molecules.
Safety Precautions:
Due to the potentially hazardous nature of 2-Diazopropane, including its high flammability, proper safety precautions should be taken when handling and using 2-Diazopropane. This includes adhering to safety guidelines and protocols to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 2684-60-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,8 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2684-60:
(6*2)+(5*6)+(4*8)+(3*4)+(2*6)+(1*0)=98
98 % 10 = 8
So 2684-60-8 is a valid CAS Registry Number.
InChI:InChI=1/C3H6N2/c1-3(2)5-4/h1-2H3
2684-60-8Relevant academic research and scientific papers
UV-laser photochemistry: Retro-cleavage in the benzophenone-sensitized photolysis of Δ3-1,3,4-oxadiazolines into diazoalkanes
Adam, Waldemar,Finzel, Ralf
, p. 863 - 866 (2007/10/02)
Triplet-sensitized photolysis of 2-methoxy-2,5,5-trimethyl-Δ3-1,3,4-oxadiazoline (1a) led to the retro-cleavage products diazoalkane 2a and the ester 3a, for which the triplet diazenyl diradical 6a is postulated as precursor.
