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596105-56-5

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596105-56-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 596105-56-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,6,1,0 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 596105-56:
(8*5)+(7*9)+(6*6)+(5*1)+(4*0)+(3*5)+(2*5)+(1*6)=175
175 % 10 = 5
So 596105-56-5 is a valid CAS Registry Number.

596105-56-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(6-chloro-1H-indol-3-yl)butan-2-one

1.2 Other means of identification

Product number -
Other names -

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:596105-56-5 SDS

596105-56-5Downstream Products

596105-56-5Relevant articles and documents

Boron-Catalyzed Dehydrative Friedel-Crafts Alkylation of Arenes Using β-Hydroxyl Ketone as MVK Precursor

San, Htet Htet,Huang, Jie,Lei Aye, Seinn,Tang, Xiang-Ying

supporting information, p. 2386 - 2391 (2021/01/04)

Boron-catalyzed environmentally benign dehydrative Friedel-Crafts alkylation of indole/pyrrole and aniline derivatives with β-hydroxyl ketones has been developed for the first time. This method provides an efficient and green replacement of toxic and unst

Catalytic C-H bond functionalization with palladium(II): Aerobic oxidative annulations of indoles

Ferreira, Eric M.,Stoltz, Brian M.

, p. 9578 - 9579 (2007/10/03)

A palladium-catalyzed aerobic oxidative annulation of indoles is described. We have demonstrated that a variety of factors influence these cyclizations, and in particular the electronic nature of the pyridine ligand is crucial. It is also remarkable that these oxidative cyclizations can proceed in good yield despite background oxidative decomposition pathways, testament to the facile nature with which molecular oxygen can serve as the direct oxidant for Pd(0). We have also shown that the mechanism most likely involves initial indole palladation (formal C-H bond activation) followed by migratory insertion and β-hydrogen elimination. Copyright

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