115666-43-8

Basic information

• Product Name: 1-ACETYL-6-IODOINDOLINE
• Synonyms: 1-ACETYL-6-IODOINDOLINE
• CAS NO: 115666-43-8
• Molecular Formula: C₁₀H₁₀INO
• Molecular Weight: 287.1
• Mol File: 115666-43-8.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-ACETYL-6-IODOINDOLINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-ACETYL-6-IODOINDOLINE(115666-43-8)
• EPA Substance Registry System: 1-ACETYL-6-IODOINDOLINE(115666-43-8)

Safety Data

• Hazardous Substances Data: 115666-43-8(Hazardous Substances Data)

Usage

Class

Indoline derivative

Functional groups

Acetyl and iodine

Potential applications

a. Organic synthesis
b. Pharmaceutical research

Use as a building block

a. Synthesis of various organic compounds
b. Unique structural properties

Biological activity

a. Interest for drug development
b. Potential uses in scientific and industrial settings
These properties and contents provide a brief overview of 1-Acetyl-6-iodoindoline, highlighting its chemical structure, potential applications, and areas of interest for further research and development.

Upstream product

• 62368-29-0 1-acetyl-6-aminoindoline 
• 4769-96-4 6-nitroindole 
• 22949-08-2 1-acetyl-6-nitro-2,3-dihydroindole 
• 19727-83-4 6-nitroindoline 

Downstream Products

• 115666-46-1 6-iodo-2,3-dihydro-1H-indole 
• 115666-47-2 6-iodo-1 H-indole 
• 872876-95-4 (R,R)-3-{6-[3-(N-tert-butoxycarbonyl-2-methoxycarbonylmethylamino)-5-iodo-6-methoxyphenyl]indol-3-yl}-2-carbobenzyloxyaminopropionic acid tert-butyl ester 
• 872876-83-0 (R,R)-(6'-iodo-N-carbobenzyloxytryptophyl)-3',5'-dichloro-4'-hydroxyphenylglycine tert-butyl ester 
• 872877-18-4 (R)-6-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-N-carbobenzyloxy-6'-iodotryptophan tert-butyl ester 
• 872877-20-8 (R)-6-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-N-carbobenzyloxytryptophan 
• 872876-93-2 (R)-N-carbobenzyloxy-6'-iodotryptophan tert-butyl ester 
• 872877-29-7 (S)-N-carbobenzyloxy-6'-iodotryptophan 
• 872876-52-3 (R)-N-carbobenzyloxy-6'-iodotryptophan 

Relevant articles and documents

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A REGIOSELECTIVE AND COMMON SYNTHETIC METHOD OF DIHALOGENOINDOLES AND ITS APPLICATION FOR THE TOTAL SYNTHESES OF MARINE ALKALOIDS, 4,6-DIBROMO-, 4,6-DIBROMO-2-METHYL-, 3,4,5-TRIBROMOINDOLE

A regioselective and common synthetic method for indoles carrying two different kinds of halogens was developed and applied successfully to the total syntheses of marine alkaloids, 4,6-dibromo- and 3,4,5-tribromoindole.The first total synthesis of 4,6-dibromo-2-methylindole is also reported.