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79663-29-9

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79663-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79663-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,6 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79663-29:
(7*7)+(6*9)+(5*6)+(4*6)+(3*3)+(2*2)+(1*9)=179
179 % 10 = 9
So 79663-29-9 is a valid CAS Registry Number.

79663-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name quinolin-8-ylmethyl acetate

1.2 Other means of identification

Product number -
Other names 8-acetoxymethylquinoline

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:79663-29-9 SDS

79663-29-9Relevant articles and documents

Aerobic C-H acetoxylation of 8-methylquinoline in PdII- pyridinecarboxylic acid systems: Some structure-reactivity relationships

Wang, Daoyong,Zavalij, Peter Y.,Vedernikov, Andrei N.

, p. 4882 - 4891 (2013/09/24)

Catalytic oxidative C-H acetoxylation of 8-methylquinoline as a model substrate with O2 as oxidant was performed using palladium(II) carboxylate catalysts derived from four different pyridinecarboxylic acids able to form palladium(II) chelates of different size. A comparison of the rates of the substrate C-H activation and the O2 activation steps shows that the C-H activation step is rate-limiting, whereas the O2 activation occurs at a much faster rate already at 20 C. The chelate ring size and the chelate ring strain of the catalytically active species are proposed to be the key factors affecting the rate of the C-H activation.

Palladium-catalyzed fluorination of carbon-hydrogen bonds

Hull, Kami L.,Anani, Waseem Q.,Sanford, Melanie S.

, p. 7134 - 7135 (2007/10/03)

This communication describes the development of a new Pd-catalyzed method for the fluorination of carbon-hydrogen bonds. A key step of these transformations involves palladium-mediated carbon-fluorine couplinga much sought after, but previously unpreceden

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