208264-60-2 Usage
Uses
Used in Pharmaceutical Synthesis:
2,5-Dibromo-thiazole-4-carboxylic acid ethyl ester is utilized as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs with potential therapeutic benefits. Its unique chemical structure allows for the creation of various drug candidates that can target specific biological pathways or diseases.
Used in Agrochemical Production:
In the agrochemical industry, 2,5-Dibromo-thiazole-4-carboxylic acid ethyl ester serves as an intermediate for the production of pesticides and other crop protection agents. Its chemical properties make it suitable for the development of compounds that can effectively control pests and diseases in agriculture, thereby enhancing crop yields and quality.
Used as a Reagent in Organic Chemistry:
2,5-Dibromo-thiazole-4-carboxylic acid ethyl ester also finds application as a reagent in organic chemistry reactions. Its reactivity and functional groups enable it to participate in a variety of chemical transformations, facilitating the synthesis of complex organic molecules for research and industrial purposes.
Used in Chemical Research:
Due to its unique structure and properties, 2,5-Dibromo-thiazole-4-carboxylic acid ethyl ester is employed in chemical research to explore new reaction pathways, investigate its reactivity with different substrates, and understand its potential applications in material science and other related fields.
Check Digit Verification of cas no
The CAS Registry Mumber 208264-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,2,6 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 208264-60:
(8*2)+(7*0)+(6*8)+(5*2)+(4*6)+(3*4)+(2*6)+(1*0)=122
122 % 10 = 2
So 208264-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H5Br2NO2S/c1-2-11-5(10)3-4(7)12-6(8)9-3/h2H2,1H3
208264-60-2Relevant academic research and scientific papers
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.
Asymmetric synthesis of (1R,2S,3R)-2-acetyl-4-(1,2,3,4- tetrahydroxybutyl)thiazole
Ung, Alison T.,Pyne, Stephen G.
, p. 1395 - 1407 (2007/10/03)
Two different methods for preparing the thiazole analogue 3 of the biologically active compound (1R,2S,3R)-2-acetyl-4(5)-(1,2,3,4- tetrahydroxybutyl)imidazole 1 are reported.
