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119022-15-0

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119022-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119022-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,0,2 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 119022-15:
(8*1)+(7*1)+(6*9)+(5*0)+(4*2)+(3*2)+(2*1)+(1*5)=90
90 % 10 = 0
So 119022-15-0 is a valid CAS Registry Number.

119022-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-3-phenyl-1,6,7,8-tetrahydroquinoline-2,5-dione

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:119022-15-0 SDS

119022-15-0Downstream Products

119022-15-0Relevant articles and documents

Solvent-free microwave synthesis of 4-hydroxy-3-phenylquinolin-2(1H)-ones and variants using activated arylmalonates

Rivkin, Alexey,Adams, Bruce

, p. 2395 - 2398 (2006)

The disclosure herein describes the rapid synthesis of 4-hydroxy-3-phenylquinolin-2(1H)-ones and variants via a solvent-free microwave cyclocondensation reaction using di-(2,4,6-trichlorophenyl)-2-phenylmalonate, which improves the general scope of this reaction.

Aktive Malonester als Synthons fuer Heterocyclen: Eine Methode zur Hertstellung von 4-Hydroxy-2(1H)-pyridonen

Kappe, Thomas,Ajili, Samir,Stadlbauer, Wolfgang

, p. 463 - 468 (2007/10/02)

4-Hydroxy-2-(1H)-pyridones 3 can be obtained in excellent yields from azomethines 1 with trichlorophenylmalonates 2.The variation of the substituents in position 1,3,5 or 6, respectively is possible over a wide range.In this manner the 5,6-fused-pyridones

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