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1,2,4,5-Tetrazin-1(2H)-yl, 3,4-dihydro-2,3,4,6-tetraphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15080-57-6

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15080-57-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15080-57-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,8 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15080-57:
(7*1)+(6*5)+(5*0)+(4*8)+(3*0)+(2*5)+(1*7)=86
86 % 10 = 6
So 15080-57-6 is a valid CAS Registry Number.

15080-57-6SDS

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 1,3,5,6-tetraphenyl-verdazyl

1.2 Other means of identification

Product number -
Other names 1,3,5,6-Tetraphenyl-verdazyl

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:15080-57-6 SDS

15080-57-6Downstream Products

15080-57-6Relevant academic research and scientific papers

Tailoring Magnetic Interactions of Organic Solids: Modification of Triphenylverdazyl

Dormann, E.,Winter, H.,Dyakonow, W.,Gotschy, B.,Lang, A.,et al.

, p. 922 - 930 (2007/10/02)

Crystal Structure / Magnetism / Radicals / Spectroscopy, Electron Spin Resonance The synthesis of the free radicals 1-(4'-bromophenyl)-3,5-diphenyl-verdazyl (Br-TPV), 1-(4'-isopropylphenyl)-3,5-diphenyl-verdazyl (IP-TPV), 1,3,5,6-tetraphenyl-verdazyl (Ph-

STRENGTH OF N-H BOND IN 2,4-DIPHENYL-6-(4-X-PHENYL)-1,2,3,4-TETRAHYDRO-sym-TETRAZINES (LEUCOVERDAZYLS)

Polumbrik, O.M.,Ryabokon', I.G.,Skorobagat'ko, E.P.,Nesterenko, A.M.,Markovskii, L.N.

, p. 922 - 927 (2007/10/02)

The equilibrium contstants in the reactions of triphenylleucoverdazyls substituted at the para position of the C6-phenyl ring with 2,2,6,6-tetramethyl-4-oxopiperidin-1-oxyl in heptane were determined by spectrophotometry and ESR.At 20 deg C the equilibrium is displaced toward the formation of the more stable verdazyl radicals.The strengths of the N-H bonds in the leucoverdazyls were determined.The enthalpy of solvation of triphenylverdazyl in acetonitrile was obtained (-15.6 kJ/mole).The kinetics of exchange of hydrogen between the triphenylverdazyls and 2,2,6,6-tetramethyl-4-oxopiperidine-1-hydroxylamine in acetonitrile were studied.The mechanism of the reaction, which inlcudes the formation of a hydrogen bond between the reagents in an activated complex, is discussed.It was concluded that the reactivity of the triphenylverdazyls in the abstraction of hydrogen from organic compounds is determined to a significant degree by the strength of the N-H bond which forms in the leucoverdazyls.

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