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57147-33-8

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57147-33-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57147-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,4 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 57147-33:
(7*5)+(6*7)+(5*1)+(4*4)+(3*7)+(2*3)+(1*3)=128
128 % 10 = 8
So 57147-33-8 is a valid CAS Registry Number.

57147-33-8SDS

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 5-ethyl-8-oxo-[1,3]dioxolo[4,5-g]quinoline-7-carbonitrile

1.2 Other means of identification

Product number -
Other names 1-ethyl-1,4-dihydro-6,7-methylenedioxy-quinoline-3-carbonitrile

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:57147-33-8 SDS

57147-33-8Downstream Products

57147-33-8Relevant articles and documents

Copper-Catalyzed Synthesis of Substituted 4-Quinolones using Water as a Benign Reaction Media: Application for the Construction of Oxolinic Acid and BQCA

Gore, Babasaheb Sopan,Lee, Chein Chung,Lee, Jessica,Wang, Jeh-Jeng

, (2019/05/24)

A copper-catalyzed three-component synthetic method has been developed for the synthesis of substituted 4-quinolone derivatives from substituted 3-(2-halophenyl)-3-oxopropane, aldehydes and aq. NH3 using water as an environmentally benign reaction media. Moreover, the synthetic utility of the obtained products has been successfully applied for the synthesis of available oxolinic acid and BQCA drugs. The key features of this approach include commercially available starting materials, broad scope, and moderate to good reaction yields. Reaction with formaldehyde, and other functionalities such as ?CN, ?NO2, ?SO2Ar, and ?COAr were also successful. In addition, reaction with heterocyclic compounds such as 3-(3-bromothiophen-2-yl)-3-oxopropanenitrile proceeded smoothly to afford tetrahydrothieno[3,2-b]pyridine-6-carbonitrile analogues. The practicality of the designed protocol was confirmed by gram scale synthesis of two derivatives. (Figure presented.).

SYNTHESIS AND RADIOPROTECTIVE PROPERTIES OF OXOLINIC ACID DERIVATIVES

Kotel'nikova, N. V.,Leonova, T. S.,Ankudinov, I. V.,Znamenskii, V. V.,Yashunskii, V. G.

, p. 402 - 404 (2007/10/02)

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