26990-71-6 Usage
General Description
5-Methoxy-1,3-dimethyl-1H-pyrazole-4-carbaldehyde is a chemical compound with the molecular formula C8H10N2O2. It is a pyrazole derivative with a methoxy group and two methyl groups attached to the core structure. 5-METHOXY-1,3-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE has potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science. It is commonly used as a building block in the synthesis of other organic compounds, and its unique structure makes it useful for the development of new drugs and materials. Additionally, it has also been studied for its potential biological and pharmacological properties. Overall, 5-Methoxy-1,3-dimethyl-1H-pyrazole-4-carbaldehyde is a versatile compound with potential uses in multiple fields.
Check Digit Verification of cas no
The CAS Registry Mumber 26990-71-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,9 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26990-71:
(7*2)+(6*6)+(5*9)+(4*9)+(3*0)+(2*7)+(1*1)=146
146 % 10 = 6
So 26990-71-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2O2/c1-5-6(4-10)7(11-3)9(2)8-5/h4H,1-3H3
26990-71-6Relevant articles and documents
Synthesis and bioactivities of novel pyrazole oxime derivatives containing a 5-trifluoromethylpyridyl moiety
Dai, Hong,Chen, Jia,Li, Hong,Dai, Baojiang,He, Haibing,Fang, Yuan,Shi, Yujun
, (2016/04/20)
In this study, in order to find novel biologically active pyrazole oxime compounds, a series of pyrazole oxime derivatives containing a 5-trifluoromethylpyridyl moiety were synthesized. Preliminary bioassays indicated that most title compounds were found to display good to excellent acaricidal activity against Tetranychus cinnabarinus at a concentration of 200 μg/mL, and some designed compounds still showed excellent acaricidal activity against Tetranychus cinnabarinus at the concentration of 10 μg/mL, especially since the inhibition rates of compounds 8e, 8f, 8l, 8m, 8n, 8p, and 8q were all 100.00%. Interestingly, some target compounds exhibited moderate to good insecticidal activities against Plutella xylostella and Aphis craccivora at a concentration of 200 μg/mL; furthermore, compounds 8e and 8l possessed outstanding insecticidal activities against Plutella xylostella under the concentration of 50 μg/mL.
