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58787-04-5

58787-04-5

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58787-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58787-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,8 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58787-04:
(7*5)+(6*8)+(5*7)+(4*8)+(3*7)+(2*0)+(1*4)=175
175 % 10 = 5
So 58787-04-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H9NO/c1-8-6-7-14-12-9-4-2-3-5-10(9)13(15)11(8)12/h2-7H,1H3

58787-04-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylindeno[1,2-b]pyridin-5-one

1.2 Other means of identification

Product number -
Other names 1-methyl-4-azafluorenone

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:58787-04-5 SDS

58787-04-5Relevant articles and documents

Facile Synthesis of Onychines

Arita, Mao,Yokoyama, Soichi,Asahara, Haruyasu,Nishiwaki, Nagatoshi

, p. 2007 - 2013 (2019/04/26)

The FeCl 3 -mediated condensation of an α-phenylenamino ester and an enone proceeds efficiently to afford a 2-phenylnicotinate. The subsequent intramolecular Friedel-Crafts reaction yielded an onychine framework. Modifications at the 2-, 3-, and 8-positions of the onychine framework were easily achieved by altering the enamino esters and enones, which facilitated the discovery of potentially bioactive compounds.

Synthesis of substituted azafluorenones from dihalogeno diaryl ketones by palladium-catalyzed auto-tandem processes

Marquise, Nada,Dorcet, Vincent,Chevallier, Floris,Mongin, Florence

supporting information, p. 8138 - 8141 (2015/01/09)

Substituted azafluorenones were synthesized from different dihalogeno diaryl ketones under palladium catalysis by combining either Suzuki or Heck coupling with direct cyclizing arylation. Conditions were identified to allow both auto-tandem processes to p

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