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Benzo[b]thiophene-3-carboxylic acid, 7-benzoyl-2,3-dihydrois a chemical compound with potential pharmacological applications. It belongs to the class of benzoyl compounds and features a benzothiophene ring structure with carboxylic acid and benzoyl functional groups. Known for its anti-inflammatory and analgesic properties, Benzo[b]thiophene-3-carboxylic acid, 7-benzoyl-2,3-dihydro- is a promising candidate for the development of pharmaceuticals. Its unique structure and properties make it a valuable component for further research and potential applications in the medical field.

93669-93-3

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93669-93-3 Usage

Uses

Used in Pharmaceutical Industry:
Benzo[b]thiophene-3-carboxylic acid, 7-benzoyl-2,3-dihydrois used as an active pharmaceutical ingredient for its anti-inflammatory and analgesic properties. It is particularly valuable in the development of medications aimed at treating pain and reducing inflammation, offering a potential alternative or adjunct to existing treatments.
Used in Research and Development:
In the field of medicinal chemistry, Benzo[b]thiophene-3-carboxylic acid, 7-benzoyl-2,3-dihydroserves as a key compound for research and development. Its unique structure allows scientists to explore its potential interactions with biological targets, paving the way for the discovery of new drugs and therapeutic agents.
Used in Drug Design and Synthesis:
Benzo[b]thiophene-3-carboxylic acid, 7-benzoyl-2,3-dihydrois utilized in drug design and synthesis processes. Its benzothiophene ring and functional groups provide a versatile template for the creation of new molecules with improved pharmacological properties, such as enhanced potency, selectivity, and reduced side effects.
Used in Drug Delivery Systems:
To enhance the bioavailability and therapeutic efficacy of Benzo[b]thiophene-3-carboxylic acid, 7-benzoyl-2,3-dihydro-, it can be incorporated into various drug delivery systems. These systems may include nanoparticles, liposomes, or other carriers, which can improve the compound's solubility, stability, and targeted delivery to specific tissues or cells.

Check Digit Verification of cas no

The CAS Registry Mumber 93669-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,6,6 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 93669-93:
(7*9)+(6*3)+(5*6)+(4*6)+(3*9)+(2*9)+(1*3)=183
183 % 10 = 3
So 93669-93-3 is a valid CAS Registry Number.

93669-93-3Downstream Products

93669-93-3Relevant academic research and scientific papers

7-Aroyl-2,3-dihydrobenzofuran-3-carboxylic Acids and 7-Benzoyl-2,3-dihydrobenzothiophene-3-carboxylic Acids as Analgesic Agents

Boyle, Elizabeth A.,Mangan, Frank R.,Markwell, Roger E.,Smith, Stephen A.,Thomson, Michael J.,et al.

, p. 894 - 898 (2007/10/02)

The synthesis of a series of 7-aroyl-2,3-dihydrobenzofuran-3-carboxylic acids and 7-benzoyl-2,3-dihydrobenzothiophene-3-carboxylic acids is described.The isomeric 4-benzoyl-1,3-dihydrobenzofuran-1-carboxylic acid was also prepared.Compounds were

Anti-inflammatory and analgesic benzothiophene and benzafuran derivatives, compositions, and method of use therefor

-

, (2008/06/13)

Compounds of formula (I): STR1 wherein: Ar is phenyl optionally substituted in the o-, m- or p-position by C1-4 alkyl, C1-4 alkoxy, trifluoromethyl, bromo, chloro or fluoro, pyrryl optionally N-substituted by C1-4 alkyl, 2-furyl or 2-thienyl either optionally substituted in the 3-, 4- or 5-position by methyl, chloro or bromo, or 3-furyl or 3-thienyl; X is oxygen, sulphur, sulphoxide or sulphone, Y is methylene, R1 and R3 are hydrogen or C1-4 alkyl, and R2 is hydrogen, C1-4 alkyl, fluoro, chloro or bromo, or X is methylene, Y is oxygen, R1 and R3 are both hydrogen, and R2 is hydrogen, fluoro, chloro or bromo; and R4 is hydrogen or C1-4 alkyl, or a salt thereof, have analgesic and/or anti-inflammatory activity.

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