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6220-65-1

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6220-65-1 Usage

General Description

Lutidinaldehyde, also known as 2-Pyridinecarboxaldehyde, is a yellowish and aromatic organic chemical compound. It is primarily categorized under the group of pyridines, characterized by the presence of a heterocyclic aromatic ring in its molecular structure. Lutidinaldehyde has a molecular weight of 107.14 g/mol and its molecular formula is C6H5NO. Lutidinaldehyde is commonly used as a precursor in the synthesis of various pharmaceutical drugs and organic chemical compounds due to its reactivity. However, exposure to this compound is harmful as it may cause severe skin burns, eye damage and could be fatal if swallowed and enters the airways.

Check Digit Verification of cas no

The CAS Registry Mumber 6220-65-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,2 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6220-65:
(6*6)+(5*2)+(4*2)+(3*0)+(2*6)+(1*5)=71
71 % 10 = 1
So 6220-65-1 is a valid CAS Registry Number.

6220-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name pyridine-2,4-dicarbaldehyde

1.2 Other means of identification

Product number -
Other names Pyridindialdehyd-(2,4)

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:6220-65-1 SDS

6220-65-1Downstream Products

6220-65-1Relevant articles and documents

Selective DIBAL-H Monoreduction of a Diester Using Continuous Flow Chemistry: From Benchtop to Kilo Lab

Uhlig, Nick,Martins, Andrew,Gao, Detian

, p. 2326 - 2335 (2020/06/08)

Herein we report a selective DIBAL-H-mediated reduction of a heterocyclic diester to the corresponding monoaldehyde using continuous flow chemistry. The use of continuous flow enabled operation at lower temperatures and better control of the reaction time, thereby allowing for a significant increase in reaction selectivity and yield compared with batch conditions. The reaction's development as a continuous flow process and its scale-up from laboratory gram scale to multikilogram scale are discussed, including design of experiments studies to probe the optimal reaction window.

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