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1,2,4-Triazolidin-1-yl, 3,5-dioxo-4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80540-38-1

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80540-38-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80540-38-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,4 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80540-38:
(7*8)+(6*0)+(5*5)+(4*4)+(3*0)+(2*3)+(1*8)=111
111 % 10 = 1
So 80540-38-1 is a valid CAS Registry Number.

80540-38-1SDS

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 4-Phenylurazolyl radical

1.2 Other means of identification

Product number -
Other names 4-phenylurazolyl

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:80540-38-1 SDS

80540-38-1Downstream Products

80540-38-1Relevant academic research and scientific papers

4-Phenyl-4H-1,2,4-triazoline-3,5-dione, an Efficient Spin Trap for Carbon- and Metal-Centered Radicals

Alberti, Angelo,Pedulli, Gian Franco

, p. 2544 - 2549 (2007/10/02)

The spin adducts between a variety of organic or organometallic radicals and 4-phenyl-4H-1,2,4-triazoline-3,5-dione (Ph-TAD) have been investigated by ESR spectroscopy.Because of its reactivity toward metal-centered radicals which do not easily add to nitroso derivatives or nitrones, Ph-TAD can provide a valuable alternative to these more popular radical scavengers.The ambiguity present in the literature about the ESR parameters of some of the resulting 4-phenylurazolyl radicals is discussed.

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