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1-(3-phenylpropyl)-1H-indole-2,3-dione, also known as 3-phenylpropylisoindolin-1-one, is a synthetic compound with a molecular formula of C17H15NO2. It is a yellow solid that is used in research and laboratory settings as a precursor for the synthesis of various compounds. This chemical has been studied for its potential therapeutic applications, such as its anti-inflammatory and anticancer properties. Its chemical structure contains a substituted indole ring with a phenylpropyl side chain and a ketone functional group, making it a valuable intermediate in organic synthesis. Overall, 1-(3-phenylpropyl)-1H-indole-2,3-dione is a versatile compound with potential applications in pharmaceutical research and development.

404006-85-5

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404006-85-5 Usage

Uses

Used in Pharmaceutical Research and Development:
1-(3-phenylpropyl)-1H-indole-2,3-dione is used as a precursor in the synthesis of various compounds for pharmaceutical research and development. Its unique chemical structure allows for the creation of a wide range of molecules with potential therapeutic applications.
Used in Organic Synthesis:
1-(3-phenylpropyl)-1H-indole-2,3-dione is used as an intermediate in organic synthesis due to its substituted indole ring and phenylpropyl side chain. This versatile compound can be used to create a variety of molecules with different properties and potential uses.
Used in Anti-inflammatory Applications:
1-(3-phenylpropyl)-1H-indole-2,3-dione has been studied for its potential anti-inflammatory properties. It may be used as a therapeutic agent for conditions characterized by inflammation, such as arthritis or other autoimmune disorders.
Used in Anticancer Applications:
1-(3-phenylpropyl)-1H-indole-2,3-dione has also been studied for its potential anticancer properties. It may be used as a therapeutic agent in the treatment of various types of cancer, either alone or in combination with other chemotherapeutic drugs.
Used in Drug Delivery Systems:
To enhance the efficacy and bioavailability of 1-(3-phenylpropyl)-1H-indole-2,3-dione, novel drug delivery systems have been developed. These systems aim to improve the compound's delivery to target cells and tissues, potentially increasing its therapeutic effects and reducing side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 404006-85-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,4,0,0 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 404006-85:
(8*4)+(7*0)+(6*4)+(5*0)+(4*0)+(3*6)+(2*8)+(1*5)=95
95 % 10 = 5
So 404006-85-5 is a valid CAS Registry Number.

404006-85-5Relevant academic research and scientific papers

Design and synthesis of N-alkyl oxindolylidene acetic acids as a new class of potent Cdc25A inhibitors

Shimazawa, Rumiko,Kuriyama, Masami,Shirai, Ryuichi

, p. 3350 - 3353 (2008)

The oxindolylidene acetic acids having long N-alkyl chains exhibited strong inhibitory activity toward dual specificity phosphatase Cdc25A.

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