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1-ACETYL-5-BROMO-7-IODOINDOLINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

115666-44-9

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115666-44-9 Usage

Type of compound

Chemical compound

Derivative of

Indoline (a heterocyclic compound containing a six-membered ring with nitrogen)

Substituents

Bromo and iodo

Functional group

Acetyl

Potential applications

Organic synthesis and medicinal chemistry

Reactivity

Unique structure and reactivity

Utilization

Bromo and iodo substituents can be used in various reactions for the synthesis of other complex organic compounds

Biological activities

Indoline core has been found to possess interesting biological activities

Value

Valuable building block for drug development

Versatility

Potential applications in diverse scientific fields

Check Digit Verification of cas no

The CAS Registry Mumber 115666-44-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,6,6 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 115666-44:
(8*1)+(7*1)+(6*5)+(5*6)+(4*6)+(3*6)+(2*4)+(1*4)=129
129 % 10 = 9
So 115666-44-9 is a valid CAS Registry Number.

115666-44-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(5-bromo-7-iodo-2,3-dihydroindol-1-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-Acetyl-5-bromo-7-iodoindoline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:115666-44-9 SDS

115666-44-9Downstream Products

115666-44-9Relevant academic research and scientific papers

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

Ohta, Toshiharu,Yamato, Yoshinori,Tahira, Hiroko,Somei, Masanori

, p. 2817 - 2822 (2007/10/02)

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.

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