1178886-89-9 Usage
Uses
Used in Medicinal Chemistry and Drug Development:
Tert-Butyl (4-bromo-5-chlorothiazol-2-yl)(phenyl)carbamate serves as a building block in the synthesis of potential pharmaceutical agents. Its unique structural features, including the thiazole ring and phenyl group, make it a valuable component in the development of new drugs with specific therapeutic properties.
Used in Pesticide or Fungicide Formulations:
Due to its structural features, Tert-Butyl (4-bromo-5-chlorothiazol-2-yl)(phenyl)carbamate may possess pesticidal or fungicidal properties. It can be incorporated into formulations to control pests and fungi in agricultural and other settings, contributing to crop protection and maintaining ecosystem balance.
Safety and Handling:
Tert-Butyl (4-bromo-5-chlorothiazol-2-yl)(phenyl)carbamate should be handled and stored according to proper safety protocols. This ensures that exposure is minimized, and the compound's stability is maintained, preventing any potential hazards associated with its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1178886-89-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,8,8,8 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1178886-89:
(9*1)+(8*1)+(7*7)+(6*8)+(5*8)+(4*8)+(3*6)+(2*8)+(1*9)=229
229 % 10 = 9
So 1178886-89-9 is a valid CAS Registry Number.
1178886-89-9Relevant academic research and scientific papers
Polyarylated thiazoles via a combined halogen dance - Cross-coupling strategy
Schnuerch, Michael,Khan, Ather Farooq,Mihovilovic, Marko D.,Stanetty, Peter
experimental part, p. 3228 - 3236 (2009/12/09)
The application of the halogen dance reaction for the synthesis of starting materials for cross-coupling reactions is reported. The obtained compounds were then successfully applied, in sequential Stille and Suzuki-Miyaura cross-coupling reactions to obta
Halogen dance and sequential cross-coupling on 2-anilinothiazoles
Khan, Ather Farooq,Schnuerch, Michael,Mihovilovic, Marko D.,Stanetty, Peter
experimental part, p. 171 - 174 (2010/04/23)
A series of 4-bromo-5-halo and 4-bromo-5-organometal-2-anilinothiazole derivatives were prepared via the halogen dance (HD) reaction. Subsequent Pd-catalyzed Stille and Suzuki-Miyaura cross-coupling reactions were performed in a sequential manner to obtai
