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1-p-acetamidophenoxymethanecarbonyl-N'-<3',5'-dimethyl>pyrazole is a complex organic compound with the molecular formula C16H18N2O4. It is characterized by a pyrazole ring with two methyl groups at the 3' and 5' positions, and a phenoxymethanecarbonyl group connected to a p-acetamidophenyl moiety. This chemical structure suggests potential applications in pharmaceuticals or as a chemical intermediate due to its ability to form stable complexes and its reactivity. The compound's specific properties, such as solubility, stability, and potential biological activity, would need to be further investigated to understand its full range of applications and effects.

75129-62-3

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75129-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75129-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,2 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 75129-62:
(7*7)+(6*5)+(5*1)+(4*2)+(3*9)+(2*6)+(1*2)=133
133 % 10 = 3
So 75129-62-3 is a valid CAS Registry Number.

75129-62-3Downstream Products

75129-62-3Relevant academic research and scientific papers

Synthesis and antibacterial activity of a series 1-aryl-2-mercapto-5--1,3,4-triazoles, thiadiazoles and 2--3,4,5-trisubstituted pyrazoles

Nagrund, L. V. G.,Reddy, G. R. N.,Hariprasad, V.

, p. 499 - 502 (2007/10/03)

A series of new 1-aryl-2-mercapto-5--1,3,4-triazoles, 2-arylamino-5--1,3,4-thiadiazoles, p-acetamido(phenoxy)acetyl thio-semicarbazides and 2--3-amino-4-carboxamido-5-methylthiopyrazole have been prepared and evaluated for comparative antibacterial activity.The antibacterial activity of the target compounds and their relevant reference agent have been determined in vitro using serial 2-fold dilution technique on an assortment of Gram negative and Gram positive organisms.It has been observed that the in vitro antibacterial activity of cyclized 1,3,4-triazoles and 1,3,4-thiadiazoles are significantly greater than thiosemicarbazides.The derivatives 4b, 5b have better in vitro antibacterial activity.

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