76998-79-3 Usage
Uses
Used in Medicinal Chemistry Research:
(6-phenyl-2,3-dihydroimidazo[2,1-b][1,3]thiazol-5-yl)methyl ethylcarbamate is used as a research compound for exploring its potential pharmacological properties. Its unique structure allows it to target specific biological pathways, which can be beneficial for the development of new drugs to treat certain diseases.
Used in Agrochemicals:
In the agrochemical industry, (6-phenyl-2,3-dihydroimidazo[2,1-b][1,3]thiazol-5-yl)methyl ethylcarbamate may be utilized as an active ingredient or a component in the formulation of various products, such as pesticides or herbicides, due to its potential biological activities.
Used as an Intermediate in Organic Synthesis:
(6-phenyl-2,3-dihydroimidazo[2,1-b][1,3]thiazol-5-yl)methyl ethylcarbamate can also be used as an intermediate in the synthesis of other organic compounds. Its unique structure makes it a valuable building block for creating more complex molecules with specific applications in various industries.
Overall, the chemical structure of (6-phenyl-2,3-dihydroimidazo[2,1-b][1,3]thiazol-5-yl)methyl ethylcarbamate makes it a versatile molecule with potential applications in various scientific and industrial fields, including medicinal chemistry, agrochemicals, and organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 76998-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,9 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76998-79:
(7*7)+(6*6)+(5*9)+(4*9)+(3*8)+(2*7)+(1*9)=213
213 % 10 = 3
So 76998-79-3 is a valid CAS Registry Number.
76998-79-3Relevant academic research and scientific papers
COMPOSTI A PRESUNTA ATTIVITA ANTITUMORALE. VI - Esteri di 5-idrossimetilimidazotiazoli 6-sostituiti
Andreani, A.,Bonazzi, D.,Rambaldi, M.
, p. 896 - 901 (2007/10/02)
6-Substituted 5-hydroxymethylimidazothiazoles and 2,3-dihydro-5-hydroxymethylimidazothiazoles (VII - XII) were prepared by reducing the corresponding aldehydes (I - VI) with NaBH4.Among the acetic (VII a - XII a), methylcarbamic (VII b - XII b) and ethylcarbamic esters (VII c - XII c), compound (VII a) was active in a preliminary P388 leukemia test.
