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hydrochloride of leucoverdazyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72024-80-7

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72024-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72024-80-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,2 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 72024-80:
(7*7)+(6*2)+(5*0)+(4*2)+(3*4)+(2*8)+(1*0)=97
97 % 10 = 7
So 72024-80-7 is a valid CAS Registry Number.

72024-80-7SDS

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 hydrochloride of leucoverdazyl

1.2 Other means of identification

Product number -
Other names leucoverdazyl hydrochloride

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:72024-80-7 SDS

72024-80-7Downstream Products

72024-80-7Relevant academic research and scientific papers

KINETICS AND MECHANISM OF MONOMOLECULAR HETEROLYSIS OF FRAMEWORK COMPOUNDS. V. IONIZATION-FRAGMENTATION PROCESS IN DECOMPOSITION OF 1-ADAMANTYL CHLOROFORMATE

Ponomareva, E. A.,Yavorskaya, I. F.,Dvorko, G. V.

, p. 477 - 489 (2007/10/02)

The decomposition of 1-adamantyl chloroformate in acetonitrile, nitrobenzene, benzene, and isopropyl and tert-butyl alcohols in the presence of triphenylverdazyls as internal indicator was investigated preparatively and kinetically.In nitrobenzene small addition of water increase the reaction rate, and additions of tetraethylammonium halides reduce it.In isopropyl and tert-butyl alcohols and in nitrobenzene in the presence of tetraethylammonium halides the reaction rate depends on the nature of the substituent in the verdazyl.The reaction rate increases linearly with increase in the dielectric constant of the medium.It is assumed that an intimate ion pair is formed at the first stage of the reaction and undergoes fragmentation in the controlling stage to 1-adamantyl chloride or is converted into a solvent-separated ion pair.The latter reacts with the verdazyl or undergoes fragmentation to 1-adamantyl chloride.

KINETICS AND MECHANISM OF MONOMOLECULAR HETEROLYSIS OF FRAMEWORK COMPOUNDS. II. IONIZATION OF 1-ADAMANTYL IODIDE IN ACETONITRILE

Ponomareva, E. A.,Tarasenko, P. V.,Yurchenko, A. G.,Dvorko, G. F.

, p. 2191 - 2203 (2007/10/02)

The heterolysis of 1-adamantyl iodide in acetonitrile was studied preparatively and kinetically (in the presence of triphenylverdazyl as internal indicator).Additions of LiClO4, Et4N+ClO4-, Et4N+OTs-, Et4N+I-, and Et4N+Br- do not affect the reaction rate; the normal salt effect and the salt effect of the law of mass action do not appear.Additions of water increase the reaction rate a little, while additions of LiBr, Bu4N+NO3-, LiCl, and Et4N+Cl- reduce it greatly.It is suggested that an intimate ion pair of the substrate is converted into a solvent- separated ion pair in the controlling stage of the reaction.

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