1826-21-7 Usage
Uses
Used in Pharmaceutical Industry:
4-(4-Methoxy-phenyl)-thiazole is used as a key intermediate in the synthesis of various pharmaceutical compounds for its ability to enhance the biological activity and pharmacological properties of the resulting drugs. Its incorporation into drug molecules can improve their efficacy, selectivity, and safety profiles.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(4-Methoxy-phenyl)-thiazole is utilized as a building block for the development of novel agrochemicals, such as pesticides and herbicides. Its unique chemical structure allows for the creation of compounds with improved pesticidal activity, selectivity, and environmental compatibility.
Used in Materials Science:
4-(4-Methoxy-phenyl)-thiazole is employed as a component in the development of advanced materials with specific properties, such as conductivity, magnetism, or optical characteristics. Its incorporation into these materials can lead to the creation of innovative products with applications in various fields, including electronics, sensors, and energy storage.
Used in Drug Discovery and Development:
4-(4-Methoxy-phenyl)-thiazole is used as a starting material or scaffold in drug discovery and development processes. Its unique chemical properties and structural features make it a promising candidate for the design and synthesis of new bioactive compounds with potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1826-21-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1826-21:
(6*1)+(5*8)+(4*2)+(3*6)+(2*2)+(1*1)=77
77 % 10 = 7
So 1826-21-7 is a valid CAS Registry Number.
1826-21-7Relevant academic research and scientific papers
Programmed synthesis of arylthiazoles through sequential C-H couplings
Tani, Satoshi,Uehara, Takahiro N.,Yamaguchi, Junichiro,Itami, Kenichiro
, p. 123 - 135 (2014/01/06)
A programmed synthesis of privileged arylthiazoles via sequential C-H couplings catalyzed by palladium or nickel catalysts has been accomplished. This versatile protocol can supply all possible arylthiazole substitution patterns (2-aryl, 4-aryl, 5-aryl, 2
Novel series of 3-amino-N-(4-aryl-1,1-dioxothian-4-yl)butanamides as potent and selective dipeptidyl peptidase IV inhibitors
Nitta, Aiko,Fujii, Hideaki,Sakami, Satoshi,Satoh, Mikiya,Nakaki, Junko,Satoh, Shiho,Kumagai, Hiroki,Kawai, Hideki
, p. 7036 - 7040 (2013/01/15)
A series of novel 3-amino-N-(4-aryl-1,1-dioxothian-4-yl)butanamides were investigated as dipeptidyl peptidase IV (DPP-4) inhibitors. Introduction of a 4-phenylthiazol-2-yl group showed highly potent DPP-4 inhibitory activity. Among various derivatives, (3R)-3-amino-N-(4-(4-phenylthiazol-2-yl)-tetrahydro-2H- thiopyran-4-yl)-4-(2,4,5-trifluorophenyl)butanamide 1,1-dioxide (30) reduced blood glucose excursion in an oral glucose tolerance test by oral administration.
