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6190-94-9

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6190-94-9 Usage

Derivative of

Pyridine

Usage

Synthesis of coordination polymers and metal-organic frameworks; building block in organic synthesis; potential applications in drug design and catalysis

Physical state

Colorless liquid

Odor

Characteristic

Health hazard

Moderate (potential irritant and narcotic effects on the respiratory system)

Handling and storage

Appropriate safety precautions required

Check Digit Verification of cas no

The CAS Registry Mumber 6190-94-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,9 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6190-94:
(6*6)+(5*1)+(4*9)+(3*0)+(2*9)+(1*4)=99
99 % 10 = 9
So 6190-94-9 is a valid CAS Registry Number.

6190-94-9SDS

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 N-(2,2-diethoxyethyl)-1-pyridin-2-ylmethanimine

1.2 Other means of identification

Product number -
Other names pyridin-2-ylmethyleneamino-acetaldehyde diethyl acetal

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:6190-94-9 SDS

6190-94-9Relevant articles and documents

Convergent and Practical Synthesis of Fluorescent Triphenylamine Derivatives and Their Localization in Living Cells

Auvray, Marie,Franck, Xavier,Gallavardin, Thibault,Leleu, Stéphane,Mahuteau-Betzer, Florence,Mougeot, Romain,Oger, Samuel

, (2022/02/09)

In the search for new fluorescent triphenylamine (TP) derivatives, we studied the influence of the position and substitution of diverse heterocyclic substituents. A library of 10 fluorescent triphenylamines bearing either oxazoles or thiazoles and pyridiniums, substituted at different positions has been developed. The approach is based on a convergent C?H activation reaction between pyridine-oxazoles or pyridine-thiazoles and di-iodo triphenylamine. We showed that the nature and substitution pattern of the 5-membered- (oxazole, thiazole) or 6-membered heterocycle (pyridine) has a strong influence on their fluorescence properties and on their localization in living cells as they stain either the nucleus or mitochondria.

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