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Benzo[b]thiophene-3-carboxylic acid, 2-(acetylamino)-6-bromo-7-hydroxy-, ethyl ester is a complex chemical compound that features a benzo[b]thiophene ring fused to a carboxylic acid group. This structure is further adorned with an acetylamino group, a bromine atom, and a hydroxyl group. The carboxylic acid is esterified with an ethyl group, enhancing its stability and bioavailability. Benzo[b]thiophene-3-carboxylic acid,
2-(acetylamino)-6-bromo-7-hydroxy-, ethyl ester may serve as a valuable synthetic intermediate or building block in the pharmaceutical industry, with potential applications in drug discovery. Due to its complex nature and potential hazards, it is crucial to handle this chemical with caution.

113407-93-5

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113407-93-5 Usage

Uses

Used in Pharmaceutical Industry:
Benzo[b]thiophene-3-carboxylic acid, 2-(acetylamino)-6-bromo-7-hydroxy-, ethyl ester is used as a synthetic intermediate for the development of new pharmaceutical compounds. Its unique structure and functional groups make it a promising candidate for the synthesis of novel drugs with potential therapeutic applications.
Used in Drug Discovery:
In the field of drug discovery, Benzo[b]thiophene-3-carboxylic acid, 2-(acetylamino)-6-bromo-7-hydroxy-, ethyl ester is used as a building block to construct more complex molecules with potential medicinal properties. Its presence in various chemical libraries allows researchers to explore its potential interactions with biological targets, leading to the identification of new drug candidates.
Used in Chemical Research:
Benzo[b]thiophene-3-carboxylic acid, 2-(acetylamino)-6-bromo-7-hydroxy-, ethyl ester is also used in chemical research to study its reactivity, stability, and potential transformations. This knowledge can be applied to develop new synthetic routes and improve the overall efficiency of drug synthesis processes.
Used in Material Science:
Although not explicitly mentioned in the provided materials, the unique structure of Benzo[b]thiophene-3-carboxylic acid, 2-(acetylamino)-6-bromo-7-hydroxy-, ethyl ester may also find applications in material science, particularly in the development of new materials with specific properties, such as conductivity, optical activity, or stability. Its potential use in this field would depend on further research and exploration of its properties.

Check Digit Verification of cas no

The CAS Registry Mumber 113407-93-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,4,0 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 113407-93:
(8*1)+(7*1)+(6*3)+(5*4)+(4*0)+(3*7)+(2*9)+(1*3)=95
95 % 10 = 5
So 113407-93-5 is a valid CAS Registry Number.

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