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62088-24-8

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62088-24-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62088-24-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,8 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62088-24:
(7*6)+(6*2)+(5*0)+(4*8)+(3*8)+(2*2)+(1*4)=118
118 % 10 = 8
So 62088-24-8 is a valid CAS Registry Number.

62088-24-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-chloro-2,4-dinitrophenyl)hydrazine

1.2 Other means of identification

Product number -
Other names 1-(5-Chloro-2,4-dinitrophenyl)hydrazine

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:62088-24-8 SDS

62088-24-8Relevant articles and documents

Some Nitrogen Rich Energetic Material Synthesis by Nucleophilic Substitution Reaction from Polynitro Aromatic Compounds

?nal, Emine Kübra,Akay, M. Abdulkadir,Atakol, Orhan,Gürp?nar, Kübra,Naz?r, Hasan,Sopac?, ?. Betül,Svoboda, Ingrid,Tuncer, Yaprak Gürsoy

, p. 930 - 944 (2021/12/31)

Three new nitrogen-rich energetic compounds, N-(5-chloro-2,4-dinitrophenyl)hydrazine (1), N-(5-chloro-2,4-dinitrophenyl)guanidine (2) and N-(5-chloro-2,4-dinitrophenyl)-4-aminopyrazole (3) prepared by the nucleophilic substitution reaction of 1,3-dichloro-4,6-dinitrobenzene with hydrazine, guanidinium carbonate and 4-aminopyrazole. The compounds were characterized by 1H NMR, 13C NMR, IR and mass spectroscopy. Only compound 2 could be prepared in a suitable crystal and molecular model was determined by X-ray analysis. Compounds were investigated by TG and DSC. Thermal degradation and thermokinetic behavior were investigated by Ozawa–Flynn–Wall and Kissinger–Akahira–Sunose techniques. Compounds were observed to be prone to exothermical thermal decomposition. HOMO and LUMO levels, theoretical formation enthalpy and electrostatic maps were calculated by Gaussian09. The detonation velocity and pressure were calculated by Kamlet–Jacobs equation. The compounds were assayed for antimicrobial properties.

REGARDING THE REACTION OF S-TRICHLOROTRINITROBENZENE WITH HYDRAZINE

Lawrence, G. William,Adolph, Horst G.

, p. 1615 - 1618 (2007/10/02)

The reaction of S-trichlorotrinitrobenzene with hydrazine is shown to give 1,3-dihydrazino-4,6-dinitrobenzene (4), not S-trihydrazinotrinitrobenzene as previously reported.

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