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Quinoxaline, 6-ethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89770-34-3

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89770-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89770-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,7 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89770-34:
(7*8)+(6*9)+(5*7)+(4*7)+(3*0)+(2*3)+(1*4)=183
183 % 10 = 3
So 89770-34-3 is a valid CAS Registry Number.

89770-34-3SDS

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 6-ethoxyquinoxaline

1.2 Other means of identification

Product number -
Other names 6-ethoxy-quinoxaline

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:89770-34-3 SDS

89770-34-3Relevant academic research and scientific papers

Mild and general palladium-catalyzed synthesis of methyl aryl ethers enabled by the use of a palladacycle precatalyst

Cheung, Chi Wai,Buchwald, Stephen L.

supporting information, p. 3998 - 4001 (2013/09/02)

A general method for the Pd-catalyzed coupling of methanol with (hetero)aryl halides is described. The reactions proceed under mild conditions with a wide range of aryl and heteroaryl halides to give methyl aryl ethers in high yield.

Phototransformations of 6-X-5-nitroquinoxalines

Rtishchev,Selitrennikov

, p. 428 - 437 (2007/10/03)

Photophysical properties and photochemical activity of 6-X-5- nitroquinoxalines with electron-donor substituents (X = H, CH3, Cl, OC2H5, NH2) ortho to the nitro group were studied. The quantum yield of the formation of 5-hydroxyquinoxaline from the corresponding nitro derivative depends on the nature of the substituent and irradiation conditions. Phototransformations can go through nitro-nitrite rearrangement with the participation of two alternative T(nπ*) levels, depending on the size and electronic effects of the substituent. The latter factor is largely determined by the population on excitation of different charge-transfer states involving the nitro group.

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