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5-Methoxy-1-phenylindolin-2-one is a chemical compound with the molecular formula C16H13NO2. It is a derivative of indolin-2-one, featuring a methoxy group at the 5-position and a phenyl group at the 1-position. 5-methoxy-1-phenylindolin-2-one is known for its potential applications in the synthesis of various pharmaceuticals and organic compounds due to its unique structure. It is often used as an intermediate in the preparation of indole-based compounds, which have a wide range of biological activities, including potential use in the development of drugs for treating neurological disorders and other diseases. The compound's properties, such as its reactivity and stability, make it a valuable building block in organic synthesis and medicinal chemistry.

64053-60-7

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64053-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64053-60-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,5 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64053-60:
(7*6)+(6*4)+(5*0)+(4*5)+(3*3)+(2*6)+(1*0)=107
107 % 10 = 7
So 64053-60-7 is a valid CAS Registry Number.

64053-60-7Relevant academic research and scientific papers

Asymmetric Dieckmann Condensation towards Spirocyclic Oxindoles Catalyzed by Amino Acid-Derived Phosphonium Salts

Yu, Longhui,Liu, Jun,Wang, Hongyu,Xu, Lijun,Wu, Yufei,Zheng, Changwu,Zhao, Gang

supporting information, p. 302 - 306 (2021/11/18)

An asymmetric Dieckmann condensation towards spirocyclic oxindoles and aza-oxindoles catalyzed by amino acid-derived phosphonium salt has been developed, which expanded the applicability of asymmetric phosphonium salt catalysis in the production of 1,3-dicarbonyl compounds. This reaction is distinguished by its mild conditions (?20 °C), low catalyst loading (3–5 mol%), and broad substrate scope (25 examples). Control experiments revealed that both the catalyst‘s phosphonium skeleton and H-bonding site were required. Product transformations and a gram scale experiment were also carried out. (Figure presented.).

CYCLIC INDOLE-3-CARBOXAMIDES, THEIR PREPARATION AND THEIR USE AS PHARMACEUTICALS

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Page/Page column 77-78, (2009/09/05)

The present invention relates to cyclic indole-3-carboxamides of the Formula (I), wherein A, R, R10, R20, R30, R40, n, p and q have the meanings indicated in the claims, which are valuable pharmaceutical active compounds. Specifically, they inhibit the enzyme renin and modulate the activity of the renin-angiotensin system, and are useful for the treatment of diseases such as hypertension, for example. The invention furthermore relates to processes for the preparation of the compounds of the Formula (I), their use and pharmaceutical compositions comprising them.

Tricyclic oxindole antiinflammatory agents

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, (2008/06/13)

Tricyclic oxindole carboxamides, prepared by (a) reaction of an isocyanate with the basic ring system or (b) ammonolysis of a corresponding alkyl ester, are non-steroidal antiinflammatory agents useful in the treatment of rheumatoid arthritis.

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