102996-37-2 Usage
Uses
Used in Pharmaceutical Research:
1-(4-Bromophenyl)-5-chloro-1H-pyrazole-4-carbonitrile is used as a building block for the synthesis of various biologically active molecules in pharmaceutical research. Its unique structure and properties contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Research:
In agrochemical research, 1-(4-Bromophenyl)-5-chloro-1H-pyrazole-4-carbonitrile serves as a precursor for the synthesis of novel pesticides. Its potential to form biologically active molecules makes it a valuable component in the creation of effective and environmentally friendly pest control agents.
Used as a Reference Standard in Analytical Chemistry:
1-(4-Bromophenyl)-5-chloro-1H-pyrazole-4-carbonitrile is utilized as a reference standard in analytical chemistry. Its well-defined chemical properties allow for accurate measurements and comparisons in various analytical techniques, ensuring the reliability and accuracy of experimental results.
Used as a Reagent in Organic Synthesis:
1-(4-Bromophenyl)-5-chloro-1H-pyrazole-4-carbonitrile also serves as a reagent in organic synthesis, facilitating various chemical reactions and transformations. Its presence can enhance the efficiency and selectivity of synthetic processes, contributing to the development of new organic compounds and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 102996-37-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,9,9 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 102996-37:
(8*1)+(7*0)+(6*2)+(5*9)+(4*9)+(3*6)+(2*3)+(1*7)=132
132 % 10 = 2
So 102996-37-2 is a valid CAS Registry Number.
102996-37-2Relevant academic research and scientific papers
Herbicidal 5-halo-1-halophenyl-1H-pyrazole-4-carbonitriles
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, (2008/06/13)
The present invention is directed to herbicidal compounds of the formula STR1 wherein each R1 independently is halogen; R2 is halo or trifluoromethyl; and n is 1-5; with the provisos that when n is 1, R1 is other than fluorine, and when n is 2 and each R1 is chlorine, at least one R1 is located at a para or ortho position on the phenyl ring.
