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2-(PYRID-2-YLOXY)BENZALDEHYDE, also known as 2-formylpyridine, is a chemical compound with the molecular formula C12H9NO2. It is a pale yellow solid that is commonly used in organic synthesis and as a building block for the preparation of various heterocyclic compounds. It is often used in the pharmaceutical industry as a precursor for the synthesis of a variety of pharmaceuticals. 2-(PYRID-2-YLOXY)BENZALDEHYDE is also known for its strong odor and is often used in perfumery and fragrance formulations. Additionally, 2-(pyrid-2-yloxy)benzaldehyde has been studied for its potential biological and pharmacological activities, making it a versatile and important compound in the field of chemistry and drug development.

141580-71-4

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141580-71-4 Usage

Uses

Used in Pharmaceutical Industry:
2-(PYRID-2-YLOXY)BENZALDEHYDE is used as a precursor in the synthesis of various pharmaceuticals for its ability to form heterocyclic compounds, which are essential in the development of new drugs.
Used in Perfumery and Fragrance Industry:
2-(PYRID-2-YLOXY)BENZALDEHYDE is used as a component in perfumery and fragrance formulations for its strong odor, contributing to the creation of unique and complex scents.
Used in Chemical Research:
2-(PYRID-2-YLOXY)BENZALDEHYDE is used in chemical research for its potential biological and pharmacological activities, allowing scientists to explore its properties and applications in the development of new compounds and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 141580-71-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,5,8 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 141580-71:
(8*1)+(7*4)+(6*1)+(5*5)+(4*8)+(3*0)+(2*7)+(1*1)=114
114 % 10 = 4
So 141580-71-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO2/c14-9-10-5-1-2-6-11(10)15-12-7-3-4-8-13-12/h1-9H

141580-71-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-pyridin-2-yloxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 2-(pyrid-2-yloxy)benzaldehyde

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:141580-71-4 SDS

141580-71-4Downstream Products

141580-71-4Relevant articles and documents

C-H functionalization of phenols using combined ruthenium and photoredox catalysis: In situ generation of the oxidant

Fabry, David C.,Ronge, Meria A.,Zoller, Jochen,Rueping, Magnus

, p. 2801 - 2805 (2015)

A combination of ruthenium and photoredox catalysis allowed the ortho olefination of phenols. Using visible light, the direct C-H functionalization of o-(2-pyridyl) phenols occurred, and diverse phenol ethers were obtained in good yields. The regeneration of the ruthenium catalyst was accomplished by a photoredox-catalyzed oxidative process.

COMPOUNDS FOR AND METHODS OF TREATING DISEASES

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Page/Page column 45, (2020/10/09)

The present invention provides compounds that modulate biological metals and to pharmaceutical compositions containing such compounds. The invention particularly relates to imidazo[1,5-a]pyridine compounds that modulate iron and are useful for the treatment of diseases, particularly neurological diseases such as Parkinson's disease (PD), Alzheimer's 5 disease (AD), Alzheimer-type dementia, Huntington's disease (HD), amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD) and multiple system atrophy (MSA).

NHC-Organocatalyzed CAr?O Bond Cleavage: Mild Access to 2-Hydroxybenzophenones

Janssen-Müller, Daniel,Singha, Santanu,Lied, Fabian,Gottschalk, Karin,Glorius, Frank

supporting information, p. 6276 - 6279 (2017/05/19)

A Truce–Smiles rearrangement of acyl-anion equivalents generated by N-heterocyclic carbene (NHC) catalysis has been achieved. The developed method includes CAr?O, CAr?S, or CAr?N bond cleavage for the formation of a CAr?C bond and enables access to 2-hydroxybenzophenones, an important structural motif that is present in several bioactive natural products. By utilizing this procedure, the alkaloid taxilamine was synthesized in three steps. DFT calculations and control experiments support a classical SNAr mechanism with a catalyst-bound Meisenheimer-type intermediate. The method features mild reaction conditions, excellent functional-group tolerance, and a broad substrate scope, including various classes of (hetero)arenes.

ACETYLENE DERIVATIVES HAVING LIPOXYGENASE INHIBITORY ACTIVITY

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, (2008/06/13)

Compounds of the structure where p and q are zero or one, but cannot both be the same, M is a pharmaceutically acceptable cation or a metabolically cleavable group, B is a valence bond or a straight or branched alkylene group, R is alkyl, cycloalkyl or --NR1 R2, where R1 and R2 are hydrogen, alkyl, cycloalkyl or alkanoyl, and A is optionally substituted carbocyclic aryl, furyl, benzo[b]furyl, thienyl, or benzo[b]thienyl are potent inhibitors of lipoxygenase enzymes and thus inhibit the biosynthesis of leukotrienes. These compounds are useful in the treatment or amelioration of allergic and inflammatory disease states.

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