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63082-45-1

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63082-45-1 Usage

Description

4-Fluoro-2-methylbenzaldehyde, also known as 4-Fluoro-o-tolualdehyde, is an organic compound belonging to the family of benzaldehyde derivatives. It is characterized by the presence of a fluorine atom at the para position and a methyl group at the ortho position relative to the aldehyde functional group. 4-Fluoro-2-methylbenzaldehyde exhibits a clear colorless to light yellow liquid appearance and is widely utilized in various research applications due to its unique chemical properties.

Uses

Used in Research and Development:
4-Fluoro-2-methylbenzaldehyde is used as a valuable research chemical for the synthesis of various complex organic molecules and pharmaceutical compounds. Its unique structure and reactivity make it a versatile building block in the development of novel drugs and advanced materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Fluoro-2-methylbenzaldehyde is employed as a key intermediate in the synthesis of various medicinal agents. Its distinct chemical properties allow for the creation of new drug candidates with potential therapeutic applications, contributing to the advancement of medical treatments.
Used in Flavor and Fragrance Industry:
4-Fluoro-2-methylbenzaldehyde is also utilized in the flavor and fragrance industry as a component in the creation of unique scents and flavors. Its distinct aromatic profile can be used to develop new fragrances or enhance existing ones, providing a wide range of possibilities for perfumers and flavorists.
Used in Material Science:
In the field of material science, 4-Fluoro-2-methylbenzaldehyde can be used as a precursor to develop novel materials with specific properties, such as improved stability, enhanced reactivity, or unique optical characteristics. Its incorporation into various materials can lead to the creation of innovative products with diverse applications.

Purification Methods

The aldehyde has been purified by gas chromatography and should be kept under N2 as it readily oxidizes in air [Burgess et al. Aust J Chem 30 543 1977].

Check Digit Verification of cas no

The CAS Registry Mumber 63082-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,8 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63082-45:
(7*6)+(6*3)+(5*0)+(4*8)+(3*2)+(2*4)+(1*5)=111
111 % 10 = 1
So 63082-45-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H7FO/c1-6-4-8(9)3-2-7(6)5-10/h2-5H,1H3

63082-45-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H26266)  4-Fluoro-2-methylbenzaldehyde, 97%   

  • 63082-45-1

  • 1g

  • 827.0CNY

  • Detail
  • Alfa Aesar

  • (H26266)  4-Fluoro-2-methylbenzaldehyde, 97%   

  • 63082-45-1

  • 10g

  • 4554.0CNY

  • Detail

63082-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Fluoro-2-methylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 4-Fluoro-o-tolualdehyde

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:63082-45-1 SDS

63082-45-1Downstream Products

63082-45-1Relevant articles and documents

Efficient and Highly Selective Solvent-Free Oxidation of Primary Alcohols to Aldehydes Using Bucky Nanodiamond

Lin, Yangming,Wu, Kuang-Hsu Tim,Yu, Linhui,Heumann, Saskia,Su, Dang Sheng

, p. 3497 - 3505 (2017/09/15)

Selective oxidation of alcohols to aldehydes is widely applicable to the synthesis of various green chemicals. The poor chemoselectivity for complicated primary aldehydes over state-of-the-art metal-free or metal-based catalysts represents a major obstacle for industrial application. Bucky nanodiamond is a potential green catalyst that exhibits excellent chemoselectivity and cycling stability for the selective oxidation of primary alcohols in diverse structures (22 examples, including aromatic, substituted aromatic, unsaturated, heterocyclic, and linear chain alcohols) to their corresponding aldehydes. The results are comparable to reported transition-metal catalysts including conventional Pt/C and Ru/C catalysts for certain substrates under solvent-free conditions. The possible activation process of the oxidant and substrates by the surface oxygen groups and defect species are revealed with model catalysts, ex situ electrochemical measurements, and ex situ attenuated total reflectance. The zigzag edges of sp2 carbon planes are shown to play a key role in these reactions.

PYRROLOY2,3-c¨PYRIDINE COMPOUND, PROCESS FOR PRODUCING THE SAME, AND USE

-

Page/Page column 45, (2010/11/27)

Provision of a compound having a superior proton pump action, which shows an antiulcer activity and the like after conversion to an in vivo proton pump inhibitor, a production method thereof and use thereof. A pyrrolo[2,3-c]pyridine compound represented by the formula: wherein each symbol is as defined in the specification.

Research and development of an efficient process for the construction of the 2,4,5-substituted pyridines of NK-1 receptor antagonists

Harrington, Peter J.,Johnston, Dave,Moorlag, Henk,Wong, Jim-Wah,Hodges, L. Mark,Harris, Les,McEwen, Gerald K.,Smallwood, Blair

, p. 1157 - 1166 (2012/12/23)

Roche has identified a 2,4,5-trisubstituted pyridine template for a new class of potent NK1 receptor antagonists. Previous strategies for construction of the pyridine core of these NK-1 receptor antagonists involved functionalization of a 2,5-disubstituted pyridine. We now report on construction of the pyridine core from commodity components. Shestopalov reported the synthesis of trans-4′-aryl-5′-cyano-1′,2′,3′, 4′-tetrahydro-6′-hydroxy-2′-oxo-1,3′-bipyridinium inner salts from 1-(2-amino-2-oxo-ethyl)pyridinium chloride, aromatic aldehydes, and ethyl cyanoacetate in the presence of a base. Reaction of these salts with phosphorus oxychloride affords 4-aryl-3-cyano-2,6-dichloropyridines. These are efficiently converted to nicotinamide precursors of the Roche NK-1 receptor antagonists by regioselective displacement of one chlorine by an amine, hydrogenolysis of the remaining chlorine, and nitrile hydrolysis.

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