96445-91-9 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-hydroxyethoxymethyl)-1,2,4-tiazole-5-carboxamide is used as an antifungal and antimicrobial agent for its strong activity against a broad spectrum of bacteria and fungi. It plays a crucial role in the development of pharmaceutical products aimed at treating and preventing infections caused by these microorganisms.
Used in Agricultural Industry:
In agriculture, 1-(2-hydroxyethoxymethyl)-1,2,4-tiazole-5-carboxamide is used as a fungicide and antimicrobial agent to protect crops from mold, mildew, and other fungal infections. Its application helps in maintaining crop health and improving yield by preventing the spread of diseases.
Used in Industrial Applications:
1-(2-hydroxyethoxymethyl)-1,2,4-tiazole-5-carboxamide is used as a biocide and preservative in various industrial processes. Its antimicrobial properties help in preventing the growth of harmful microorganisms that can cause spoilage or degradation of materials, ensuring the longevity and safety of the final products.
Used in Consumer Products:
This tiazole derivative is also utilized in the production of various consumer products, such as personal care items, cosmetics, and household cleaning agents, due to its effective antimicrobial and antifungal properties. It helps in maintaining the hygienic quality and extending the shelf life of these products by inhibiting the growth of mold and mildew.
Check Digit Verification of cas no
The CAS Registry Mumber 96445-91-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,4,4 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 96445-91:
(7*9)+(6*6)+(5*4)+(4*4)+(3*5)+(2*9)+(1*1)=169
169 % 10 = 9
So 96445-91-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H10N4O3/c7-5(12)6-8-3-9-10(6)4-13-2-1-11/h3,11H,1-2,4H2,(H2,7,12)
96445-91-9Relevant academic research and scientific papers
Modifications on the Heterocyclic Base of Acyclovir: Syntheses and Antiviral Properties
Beauchamp, Lilia M.,Dolmatch, Bart L.,Schaeffer, Howard J.,Collins, Peter,Bauer, D. J.,et al.
, p. 982 - 987 (2007/10/02)
A griup of compounds were prepared in which variations of the ring portion of the acyclovir (ACV) structure were made.These modifications included monocyclic (isocytosine, triazole, imidazole), bicyclic (8-azapurine, pyrrolo pyrimidine, pyrazolo3,
