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3-(4-chlorobenzyl)-1-methylindolin-2-one is a chemical compound with the molecular formula C16H14ClNO. It is a derivative of indolin-2-one, featuring a 4-chlorobenzyl group attached to the 3-position and a methyl group at the 1-position. 3-(4-chlorobenzyl)-1-methylindolin-2-one is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain drugs. Its structure provides a basis for further chemical modifications, which can lead to the development of new compounds with specific therapeutic or pesticidal properties. The compound's chemical properties, such as its reactivity and stability, are influenced by the presence of the chlorine atom and the indolinone ring system, making it a subject of interest in organic chemistry and medicinal chemistry research.

3335-89-5

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3335-89-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3335-89-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,3 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3335-89:
(6*3)+(5*3)+(4*3)+(3*5)+(2*8)+(1*9)=85
85 % 10 = 5
So 3335-89-5 is a valid CAS Registry Number.

3335-89-5Relevant academic research and scientific papers

Oxidative electro-organic synthesis of dimeric hexahydropyrrolo-[2,3-: B] indole alkaloids involving PCET: Total synthesis of (±)-folicanthine

Bisai, Alakesh,Khatua, Arindam,Paul, Amit,Sharma, Sulekha,Shaw, Kundan

supporting information, p. 9390 - 9395 (2021/11/17)

An efficient electrochemical oxidation strategy for the total synthesis of a dimeric hexahydropyrrolo[2,3-b]indole alkaloid, (±)-folicanthine (1b), has been envisioned. Control experiments suggest that a PCET pathway involving stepwise electron transfer f

Iridium catalysed C-3 alkylation of oxindole with alcohols under solvent free thermal or microwave conditions

Grigg, Ronald,Whitney, Simon,Sridharan, Visuvanathar,Keep, Ann,Derrick, Andrew

experimental part, p. 4375 - 4383 (2009/10/17)

Ir-catalysed alkylation of oxindole and N-methyl oxindole with a range of substituted benzyl and heteroaryl alcohols under solvent free thermal or microwave conditions afforded the corresponding C-3-monoalkylated products in high to excellent yield.

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