936240-32-3 Usage
Chemical structure
A spirocyclic compound containing a diaza ring.
Functional groups
Amide, carbonyl, and oxide groups.
Reactivity
Versatile building block for the creation of diverse chemical compounds.
Applications
Commonly used as a reagent in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals.
Biological activity
Potential biological activity and has been studied for its pharmacological properties.
Material development
May have potential applications in the development of new materials.
Research tool
Used as a research tool in the field of organic chemistry.
Solubility
Soluble in polar solvents such as water, methanol, and ethanol.
Stability
Stable under normal conditions, but sensitive to strong acids, bases, and oxidizing agents.
Melting point
The exact melting point may vary depending on the specific synthesis method and purity of the compound.
Boiling point
The exact boiling point may vary depending on the specific synthesis method and purity of the compound.
Density
The density of the compound may vary depending on its purity and the method of synthesis.
Optical properties
The compound may exhibit optical activity due to its chiral center.
Synthesis
The compound can be synthesized through various methods, such as the reaction of a suitable diazadiene with a carbonyl compound or through the cyclization of a suitable precursor.
Check Digit Verification of cas no
The CAS Registry Mumber 936240-32-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,6,2,4 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 936240-32:
(8*9)+(7*3)+(6*6)+(5*2)+(4*4)+(3*0)+(2*3)+(1*2)=163
163 % 10 = 3
So 936240-32-3 is a valid CAS Registry Number.
936240-32-3Relevant academic research and scientific papers
Cheng, Shangli,Wu, Huimin,Hu, Xianmin
, p. 297 - 308 (2007)
A convenient and efficient method for the synthesis of novel spirocyclic nitrones prepared from glycine derivatives is reported. The 1,3-cycloaddition reactions of the nitrones with alkenes lead to novel isoxazolidines in high yields and with excellent re
