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3-AMINO-5,6-DIPHENYL-1H-PYRAZIN-2-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39213-73-5

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39213-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39213-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,2,1 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 39213-73:
(7*3)+(6*9)+(5*2)+(4*1)+(3*3)+(2*7)+(1*3)=115
115 % 10 = 5
So 39213-73-5 is a valid CAS Registry Number.

39213-73-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-5,6-diphenyl-2(1H)-pyrazinone

1.2 Other means of identification

Product number -
Other names 3-amino-5,6-diphenyl-1H-pyrazin-2-one

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:39213-73-5 SDS

39213-73-5Downstream Products

39213-73-5Relevant academic research and scientific papers

ORGANIC COMPOUND FOR OPTOELECTRONIC DEVICE AND ORGANIC OPTOELECTRONIC DEVICE AND DISPLAY DEVICE

-

Paragraph 0247-0251, (2017/08/03)

The present invention relates to a compound for an organic optoelectronic device represented by chemical formula 1, an organic optoelectronic device applying the same and a display device including the organic optoelectronic device. The detailed content with respect to the chemical formula 1 are the same as defined in the specification. The compound can provide an organic optoelectronic device having high efficiency, long lifespan, etc.COPYRIGHT KIPO 2017

Studies on pyrazines; part 30: Synthesis of aminopyrazines from azidopyrazines

Sato,Matsuura,Miwa

, p. 931 - 934 (2007/10/02)

Azidopyrazines do not undergo reduction by reagents that are effective for the preparation of alkyl- or arylamines from the azides because the heterocyclic azides exist in the bicyclic form of tetrazolo[1,5-a]pyrazines. Nevertheless, the conversion into aminopyrazines was achieved by hydrogenolysis in the presence of ammonium hydroxide and palladium-on-carbon or particularly by reduction with tin(II) chloride in methanolic hydrochloric acid, in 34-87% yields. To elucidate the successful progress of the reaction, the equilibrium of azide-atetrazole was examined by 1H NMR spectroscopy in various solvents.

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