138330-03-7 Usage
Description
2-(4-methoxyphenyl)-4-methylthiazole, also known as Anisole thiazole, is a chemical compound with the molecular formula C11H11NOS. It is a thiazole derivative with a methyl and a methoxy group attached to the thiazole ring.
Uses
Used in Pharmaceutical and Agricultural Chemical Industries:
2-(4-methoxyphenyl)-4-methylthiazole is used as an intermediate in the synthesis of pharmaceuticals and agricultural chemicals. Its unique chemical structure allows it to be a versatile building block for the development of new drugs and agrochemicals.
Used in Cancer Research:
2-(4-methoxyphenyl)-4-methylthiazole is used as a potential anti-cancer agent in research studies. Its chemical properties may contribute to the development of new cancer therapies.
Used in Inflammation Research:
2-(4-methoxyphenyl)-4-methylthiazole is used as a potential anti-inflammatory agent in research studies. Its chemical properties may help in the development of new treatments for inflammatory conditions.
Used in Fragrance Industry:
2-(4-methoxyphenyl)-4-methylthiazole is used as a fragrance ingredient due to its pleasant odor. Its unique scent profile can be utilized in the creation of various fragrances for personal care and household products.
It is important to handle 2-(4-methoxyphenyl)-4-methylthiazole with care as it may pose health risks upon exposure.
Check Digit Verification of cas no
The CAS Registry Mumber 138330-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,3 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 138330-03:
(8*1)+(7*3)+(6*8)+(5*3)+(4*3)+(3*0)+(2*0)+(1*3)=107
107 % 10 = 7
So 138330-03-7 is a valid CAS Registry Number.
138330-03-7Relevant articles and documents
PdII-Catalyzed Regio- and Enantioselective Oxidative C?H/C?H Cross-Coupling Reaction between Ferrocenes and Azoles
Cai, Zhong-Jian,Liu, Chen-Xu,Gu, Qing,Zheng, Chao,You, Shu-Li
supporting information, p. 2149 - 2153 (2019/01/24)
Asymmetric C?H bond functionalization reaction is one of the most efficient and straightforward methods for the synthesis of optically active molecules. Herein we disclose an asymmetric C?H/C?H cross-coupling reaction of ferrocenes with azoles such as oxazoles and thiazoles. Palladium(II)/monoprotected amino acid (MPAA) catalytic system which exhibits excellent reactivity and regioselectivity for oxazoles and thiazoles. This method offers a powerful strategy for constructing planar chiral ferrocenes. Mechanistic studies suggest that the C?H bond cleavage of azoles is likely proceeding through a SEAr process and may not be a turnover limiting step.
