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1-Acetyl-5-fluoro-1,2-dihydro-indol-3-one is a chemical compound with the molecular formula C10H8FNO2. It is a derivative of indole, a heterocyclic aromatic organic compound, and features a fluorine atom at the 5-position, an acetyl group at the 1-position, and a ketone functional group at the 3-position. 1-Acetyl-5-fluoro-1,2-dihydro-indol-3-one is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other chemical products due to its unique structure and properties.

3802-82-2

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3802-82-2 Usage

Type of compound

Fluorinated indole derivative

Industry use

Pharmaceutical industry

Purpose

Intermediate for the synthesis of various drugs

Chemical reactivity

Can undergo various chemical reactions to form new compounds with different pharmacological properties

Additional uses

Building block in the production of agrochemicals and other fine chemicals

Significance

Unique structure and reactivity make it valuable in the field of organic synthesis and drug discovery

Check Digit Verification of cas no

The CAS Registry Mumber 3802-82-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,0 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3802-82:
(6*3)+(5*8)+(4*0)+(3*2)+(2*8)+(1*2)=82
82 % 10 = 2
So 3802-82-2 is a valid CAS Registry Number.

3802-82-2Downstream Products

3802-82-2Relevant academic research and scientific papers

Indoxyl-based umpolung strategy for the synthesis of unsymmetrical 3,3′-biindoles

Guo, Jing,Weng, Jiang,Huang, Gong-Bin,Huang, Lin-Jie,Chan, Albert S.C.,Lu, Gui

, p. 5493 - 5496 (2016/11/19)

3,3′-Bisindoles are known to be important structural motifs found in bioactive natural products, pharmaceuticals, and functional materials. Herein, a novel indoxyl-based approach was established for the synthesis of unsymmetrical 3,3′-biindoles from indoles and indoxyls. This approach generated moderate to excellent yields of the desired products (24 examples, up to 98% yield). The present method features broad substrate scope, operational simplicity, high atom economy, and utilization of non-toxic and inexpensive molecular iodine as catalyst. The applicability of this method has been demonstrated by the facile gram-scale synthesis.

Indole derivatives

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, (2008/06/13)

The invention releates to indole derivatives of the formula STR1 wherein R 1 to R 4 are, independently, hydrogen, halogen, lower-alkyl, cycloalkyl or trifluoromethyl, R 5 and R 6 are, independently, hydrogen, halogen, lower-alkyl, cycloalkyl, trifluoromet

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