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83570-43-8

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83570-43-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83570-43-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,7 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83570-43:
(7*8)+(6*3)+(5*5)+(4*7)+(3*0)+(2*4)+(1*3)=138
138 % 10 = 8
So 83570-43-8 is a valid CAS Registry Number.

83570-43-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-ethylquinoxaline

1.2 Other means of identification

Product number -
Other names Quinoxaline,5-ethyl

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:83570-43-8 SDS

83570-43-8Upstream product

83570-43-8Downstream Products

83570-43-8Relevant articles and documents

Nanoparticle-supported and magnetically recoverable nickel catalyst: A robust and economic hydrogenation and transfer hydrogenation protocol

Polshettiwar, Vivek,Baruwati, Babita,Varma, Rajender S.

experimental part, p. 127 - 131 (2010/04/22)

A magnetic nanoparticle-supported leach-proof Ni catalyst was readily prepared from inexpensive starting materials which catalyzes various hydrogenation and transfer hydrogenation reactions; high catalytic activity and ease of recovery using an external magnetic field are additional eco-friendly attributes of this catalytic system.

The Thermolysis of Polyazapentadienes. Part 2. Formation of Quinoxalines from 5-Aryl-1-phenyl-1,2,5-triazapentadienes

McNab, Hamish

, p. 1941 - 1946 (2007/10/02)

Thermolysis in the gas phase of 5-(p-substituted phenyl)-1-phenyl-1,2,5-triazapentadienes at 600 deg C and 10-2 Torr gives 6-substituted quinoxalines.The yield is ca. 30 percent, and is independent of the electronic nature of the substituent.The corresponding 5-(o-substituted) derivatives give 5-substituted quinoxalines, though the yield is lower, and quinoxaline itself is a major contaminant, due to ipso attack and ejection of the substituent. 5-(m-Substituted) derivatives give mixtures of 5- and 6-substituted quinoxalines on pyrolysis.The 5-isomer is dominant for compounds with m-alkyl substituents, while the 6-isomer is the major product for those with electron-withdrawing or electron-donating m-substituents.

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