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34813-97-3

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34813-97-3 Usage

General Description

2-(Formylamino)pyridine is a chemical compound with the molecular formula C6H6N2O. It is a pyridine derivative with a formylamino group attached to the 2-position of the pyridine ring. 2-(FORMYLAMINO)PYRIDINE is commonly used as a building block in organic synthesis for the production of various pharmaceuticals, agrochemicals, and fine chemicals. It is also used as a reagent in the synthesis of heterocyclic compounds and coordination complexes. 2-(Formylamino)pyridine exhibits a range of chemical reactivity and has potential applications in medicinal chemistry and material science. Additionally, it is considered to be a relatively stable compound under standard laboratory conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 34813-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,1 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34813-97:
(7*3)+(6*4)+(5*8)+(4*1)+(3*3)+(2*9)+(1*7)=123
123 % 10 = 3
So 34813-97-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O/c9-5-8-6-3-1-2-4-7-6/h1-5H,(H,7,8,9)

34813-97-3SDS

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 N-pyridin-2-ylformamide

1.2 Other means of identification

Product number -
Other names 2-Formylpyridine

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:34813-97-3 SDS

34813-97-3Relevant articles and documents

An Environmentally Benign, Catalyst-Free N?C Bond Cleavage/Formation of Primary, Secondary, and Tertiary Unactivated Amides

Kumar, Vishal,Dhawan, Sanjeev,Girase, Pankaj Sanjay,Singh, Parvesh,Karpoormath, Rajshekhar

, p. 5627 - 5639 (2021/11/11)

Herein, we report an operationally simple, cheap, and catalyst-free method for the transamidation of a diverse range of unactivated amides furnishing the desired products in excellent yields. This protocol is environmentally friendly and operates under extremely mild conditions without using any promoter or additives. Significantly, this strategy has been implied in the chemoselective synthesis of a pharmaceutical molecule, paracetamol, on a gram-scale with excellent yield. We anticipate that this universally applicable strategy will be of great interest in drug discovery, biochemistry, and organic synthesis.

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