178979-49-2 Usage
Uses
Used in Pharmaceutical Industry:
4-[(3-chlorophenyl)sulfanyl]-1-methyl-5-(1-methylethyl)-1H-imidazol-2-ylmethyl carbamate is used as a potential pharmaceutical agent for its possible pesticidal or medicinal properties. The carbamate group indicates that it may be effective in controlling pests, while the combination of the sulfanyl and chlorophenyl groups suggests potential for various biological and chemical interactions, making it a promising candidate for drug development.
Used in Organic Chemistry Research:
In the field of organic chemistry, 4-[(3-chlorophenyl)sulfanyl]-1-methyl-5-(1-methylethyl)-1H-imidazol-2-ylmethyl carbamate serves as a subject for further study due to its complex structure and the presence of multiple functional groups. Researchers can explore its reactivity, synthesis pathways, and potential as a building block for more complex molecules.
Used in Material Science:
The unique structure of 4-[(3-chlorophenyl)sulfanyl]-1-methyl-5-(1-methylethyl)-1H-imidazol-2-ylmethyl carbamate also makes it a candidate for material science applications. Its functional groups may allow for the development of new materials with specific properties, such as improved stability, reactivity, or selectivity in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 178979-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,9,7 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 178979-49:
(8*1)+(7*7)+(6*8)+(5*9)+(4*7)+(3*9)+(2*4)+(1*9)=222
222 % 10 = 2
So 178979-49-2 is a valid CAS Registry Number.
178979-49-2Relevant academic research and scientific papers
Imidazole derivatives as anti-HIV agents
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, (2008/06/13)
An imidazole derivative represented by general formula (I) or a salt thereof, having the effect of specifically inhibiting the growth of HIV as a pathogenic virus and being reduced in toxicity. In said formula R1 represents hydrogen, C1 -C20 alkyl, C2 -C7 alkenyl, C4 -C12 cycloalkylalkyl, etc.; R2 represents C1 -C6 alkyl, C1 -C6 acyl, hydroxyiminomethyl, hydrazonomethyl or --(CH2)n--R4 (R4 being halogeno, alkoxy, hydroxy, etc.; and n being an integer of 1 to 3); R3 represents substituted or unsubstituted C1 -C6 alkyl; X and Y represent each independently hydrogen, C1 -C3 alkyl, halogeno, or nitro; and Z represents S, SO, SO2 or CH2. STR1
