13369-72-7 Usage
Chemical class
Pyrazole derivatives It belongs to a group of chemical compounds that have a pyrazole ring in their structure.
Structural features
Allyl group and bromine atom The presence of an allyl group and a bromine atom attached to the pyrazole ring gives 1-allyl-4-bromo-1H-pyrazole its unique properties.
Potential applications
Pharmaceuticals, agrochemicals, and material science It can be used in various fields due to its unique structural features and reactivity.
Building block
Synthesis of other chemical compounds It can be used as a starting material to create new molecules with potentially useful properties.
Reagent
Organic reactions It can be used as a reagent in various organic reactions to facilitate the formation of desired products.
Research and development
Organic chemistry Its unique properties make it a subject of interest for further research and development in the field of organic chemistry.
Novel molecules
Creation of molecules with potentially useful properties Its structural features and reactivity allow for the development of new molecules with applications in various industries.
Valuable tool
Organic chemistry The compound serves as a valuable tool for chemists to explore new reactions and synthesize novel molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 13369-72-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,6 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13369-72:
(7*1)+(6*3)+(5*3)+(4*6)+(3*9)+(2*7)+(1*2)=107
107 % 10 = 7
So 13369-72-7 is a valid CAS Registry Number.
13369-72-7Relevant academic research and scientific papers
Pyrazole N-alkylation method
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Paragraph 0035; 0036, (2018/12/14)
The invention provides a pyrazole N-alkylation method. Pyrazole or pyrazole derivatives and alkyl halogenated hydrocarbons react in a solvent under the existence of quaternary ammonium salt catalysts;N-alkyl substituted pyrazole is obtained. The method provided by the invention has the advantages that the operation is simple; the cost is low; the anhydrous oxygen-free environment is not needed; heating is not needed; the yield is high; the amplified industrialized production can be easily realized.
