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Hydrazine, [2-[(2-nitrophenyl)thio]phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68207-43-2

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68207-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68207-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,0 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 68207-43:
(7*6)+(6*8)+(5*2)+(4*0)+(3*7)+(2*4)+(1*3)=132
132 % 10 = 2
So 68207-43-2 is a valid CAS Registry Number.

68207-43-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(2-nitrophenyl)sulfanylphenyl]hydrazine

1.2 Other means of identification

Product number -
Other names 2-Nitro-2'-hydrazinodiphenylsulfid

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:68207-43-2 SDS

68207-43-2Relevant academic research and scientific papers

N-Acylaminophenothiazines: Neuroprotective agents displaying multifunctional activities for a potential treatment of Alzheimer's disease

González-Mu?oz, Gema C.,Arce, Mariana P.,López, Beatriz,Pérez, Concepción,Romero, Alejandro,Barrio, Laura Del,Martín-De-Saavedra, María Dolores,Egea, Javier,León, Rafael,Villarroya, Mercedes,López, Manuela G.,García, Antonio G.,Conde, Santiago,Rodríguez-Franco, María Isabel

, p. 2224 - 2235 (2011)

We have previously reported the multifunctional profile of N-(3-chloro-10H-phenothiazin-10-yl)-3-(dimethylamino)propanamide (1) as an effective neuroprotectant and selective butyrylcholinesterase inhibitor. In this paper, we have developed a series of N-acylaminophenothiazines obtained from our compound library or newly synthesised. At micro- and sub-micromolar concentrations, these compounds selectively inhibited butyrylcholinesterase (BuChE), protected neurons against damage caused by both exogenous and mitochondrial free radicals, showed low toxicity, and could penetrate into the CNS. In addition, N-(3-chloro-10H-phenothiazin-10-yl)-2-(pyrrolidin-1-yl) acetamide (11) modulated the cytosolic calcium concentration and protected human neuroblastoma cells against several toxics, such as calcium overload induced by an l-type Ca2+-channel agonist, tau-hyperphosphorylation induced by okadaic acid and Aβ peptide.

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