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26037-41-2

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26037-41-2 Usage

Chemical family

Phenylarsine oxide family

Type of compound

Organoarsenic compound

Molecular weight

246.15 g/mol

Toxicity

Highly toxic

Carcinogenicity

Potentially carcinogenic

Usage

Research reagent, pharmaceutical production

Biological activity

Inhibitory effects on acetylcholinesterase enzyme

Role in the nervous system

Breakdown of neurotransmitter acetylcholine

Potential applications

Treatment of neurological disorders, pesticide development

Check Digit Verification of cas no

The CAS Registry Mumber 26037-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,3 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26037-41:
(7*2)+(6*6)+(5*0)+(4*3)+(3*7)+(2*4)+(1*1)=92
92 % 10 = 2
So 26037-41-2 is a valid CAS Registry Number.

26037-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-phenyl-5H-phenarsazinine

1.2 Other means of identification

Product number -
Other names 10-Phenyl-5,10-dihydro-phenarsazin

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:26037-41-2 SDS

26037-41-2Relevant articles and documents

Reaction of 10-methyl(phenyl)-5,10-dihydrophenarsazine 10-oxides with hydriodic acid

Gavrilov,Karavanov,Musin,Garieva,Musin

, p. 1212 - 1215 (2007/10/03)

We have studied the reaction of 10-methyl(phenyl)-5,10-dihydrophenarsazine 10-oxides with hydriodic acid and we have established the structure of the products by high-resolution mass spectrometry. We have shown that when the methyl group is replaced by a phenyl group in 5,10-dihydrophenarsazine 10-oxides, cleavage of the endocyclic arsenic-carbon bonds occurs. 2004 Springer Science+Business Media, Inc.

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