1125409-85-9 Usage
Uses
Used in Pharmaceutical Industry:
Ethyl 5-bromo-2-chlorothiazole-4-carboxylate is used as a synthetic intermediate for the preparation of various pharmaceuticals. Its unique chemical structure and potential biological activities make it a promising candidate for the development of new therapeutic agents.
Used in Agrochemical Industry:
Ethyl 5-bromo-2-chlorothiazole-4-carboxylate is used as a synthetic intermediate in the preparation of agrochemicals. Its antimicrobial and antiviral properties can be harnessed to develop new pesticides or fungicides to protect crops from diseases and pests.
Used in Fine Chemicals Industry:
Ethyl 5-bromo-2-chlorothiazole-4-carboxylate is used as a building block in the synthesis of other fine chemicals. Its versatile chemical structure allows for further functionalization and modification, enabling the development of novel compounds with specific applications in various industries.
Used in Chemical Research and Drug Discovery:
Ethyl 5-bromo-2-chlorothiazole-4-carboxylate is used as a key compound in chemical research and drug discovery processes. Its potential biological activities and unique chemical structure make it an attractive target for further investigation and optimization to develop new drugs and therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 1125409-85-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,5,4,0 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1125409-85:
(9*1)+(8*1)+(7*2)+(6*5)+(5*4)+(4*0)+(3*9)+(2*8)+(1*5)=129
129 % 10 = 9
So 1125409-85-9 is a valid CAS Registry Number.
1125409-85-9Relevant academic research and scientific papers
Pammer, Frank,Jager, Jakob,Rudolf, Benjamin,Sun, Yu
, p. 5904 - 5912 (2014)
Head-to-tail regioregular poly(4-alkylthiazole)s containing silylethers in the side-chains were synthesized via Kumada-Coupling polycondensation of "reversed" monomers, that were metalated at the sterically hindered 5-position. Their optical, electrochemi
Synthesis of 2,5-dihalothiazole-4-carboxylates
Okonya, John F,Al-Obeidi, Fahad
, p. 7051 - 7053 (2007/10/03)
An efficient synthesis of 2,5-dihalothiazole-4-carboxylates has been described. Halogenation of aminothiazole carboxylate with NBS or NCS and subsequent diazotization with isoamyl nitrite and halogenation with CuBr2, CuCl2 or CH2I2 provided the corresponding diahalothiazole derivatives. The four-step process described is amenable to scale-up and requires no chromatographic purification in all the steps.
