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2161380-87-4

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2161380-87-4 Usage

General Description

5-bromo-4-(4-chlorothiophen-2-yl)-2-aminothiazole is a chemical compound with a molecular formula C8H5BrClN2S2. It is a thiazole derivative with a bromo and chloro substituent on the thiophene ring. 5-bromo-4-(4-chlorothiophen-2-yl)-2-aminothiazole has potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its interesting biological activities. It has shown potential as an anti-cancer and anti-inflammatory agent. Its unique chemical structure and potential bioactivity make it a compound of interest in drug discovery and development. Further research and study on this compound may lead to its utilization in the treatment of various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 2161380-87-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,1,6,1,3,8 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2161380-87:
(9*2)+(8*1)+(7*6)+(6*1)+(5*3)+(4*8)+(3*0)+(2*8)+(1*7)=144
144 % 10 = 4
So 2161380-87-4 is a valid CAS Registry Number.

2161380-87-4Downstream Products

2161380-87-4Relevant articles and documents

Preparation method of thrombocyte increasing agent

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Paragraph 0046; 0057; 0058, (2018/03/01)

The invention relates to a preparation method of a thrombocyte increasing agent. The preparation method comprises the following steps: enabling a midbody 1 and a midbody 2 to perform amidation in the presence of a catalyst in an aprotic solvent; and adding alkali into a solvent of a midbody A to perform the alkaline hydrolysis reaction to obtain a target compound. The midbody 2 is firstly synthesized and then reacts with the midbody 1; and a synthetic route of the method is a converging reaction, so that the yield is increased, and convenience in quality control is achieved. In addition, by studying the reaction amplification feasibility, the operation such as column chromatography is avoided, the method is more suitable for an industrialized production process, and the emission of waste liquid is reduced. A product obtained by the route is high in purity, the yield is high, the pollution is small, and the preparation method is suitable for the industrialized production.

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