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2-Pyridinecarboxaldehyde,5-hydroxy-,oxime(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

147353-77-3

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147353-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147353-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,3,5 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 147353-77:
(8*1)+(7*4)+(6*7)+(5*3)+(4*5)+(3*3)+(2*7)+(1*7)=143
143 % 10 = 3
So 147353-77-3 is a valid CAS Registry Number.

147353-77-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-amino-4-phenyl-1H-pyrrole-3-carboxylate

1.2 Other means of identification

Product number -
Other names HMS1364M22

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:147353-77-3 SDS

147353-77-3Downstream Products

147353-77-3Relevant academic research and scientific papers

Pyridinium compounds

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, (2008/06/13)

Methods for using novel quaternary pyridinium compounds in inhibiting acetylcholinesterase in mammals, specifically using the quaternary pyridinium compounds in the prophylaxis and treatment of organophosphate poisoning and mammalian dementia by mimicking or opposing the actions of the natural neurotransmitter acetylcholine.

QUATERNARY PYRIDINIUM COMPOUNDS

-

, (2008/06/13)

Quaternary pyridinium compounds, their use in inhibiting acetylcholinesterase, their roles in the prophylaxis and treatment of organophosphate poisoning, their roles in anticholinesterase therapy and their roles as agents mimicking or opposing the actions of the natural neurotransmitter acetylcholine

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