Welcome to LookChem.com Sign In|Join Free

CAS

  • or

22062-53-9

Post Buying Request

22062-53-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

22062-53-9 Usage

Chemical Properties

colorless to light yelow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 22062-53-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,6 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22062-53:
(7*2)+(6*2)+(5*0)+(4*6)+(3*2)+(2*5)+(1*3)=69
69 % 10 = 9
So 22062-53-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H7FO/c1-6-2-3-8(9)4-7(6)5-10/h2-5H,1H3

22062-53-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H26799)  5-Fluoro-2-methylbenzaldehyde, 97%   

  • 22062-53-9

  • 1g

  • 368.0CNY

  • Detail
  • Alfa Aesar

  • (H26799)  5-Fluoro-2-methylbenzaldehyde, 97%   

  • 22062-53-9

  • 5g

  • 1243.0CNY

  • Detail
  • Alfa Aesar

  • (H26799)  5-Fluoro-2-methylbenzaldehyde, 97%   

  • 22062-53-9

  • 25g

  • 4052.0CNY

  • Detail

22062-53-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Fluoro-2-methylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 2-Methyl-5-fluorbenzaldehyd

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:22062-53-9 SDS

22062-53-9Relevant articles and documents

A “universal” catalyst for aerobic oxidations to synthesize (hetero)aromatic aldehydes, ketones, esters, acids, nitriles, and amides

Bartling, Stephan,Beller, Matthias,Chandrashekhar, Vishwas G.,Jagadeesh, Rajenahally V.,Rabeah, Jabor,Rockstroh, Nils,Senthamarai, Thirusangumurugan

supporting information, p. 508 - 531 (2022/02/11)

Functionalized (hetero)aromatic compounds are indispensable chemicals widely used in basic and applied sciences. Among these, especially aromatic aldehydes, ketones, carboxylic acids, esters, nitriles, and amides represent valuable fine and bulk chemicals, which are used in chemical, pharmaceutical, agrochemical, and material industries. For their synthesis, catalytic aerobic oxidation of alcohols constitutes a green, sustainable, and cost-effective process, which should ideally make use of active and selective 3D metals. Here, we report the preparation of graphitic layers encapsulated in Co-nanoparticles by pyrolysis of cobalt-piperazine-tartaric acid complex on carbon as a most general oxidation catalyst. This unique material allows for the synthesis of simple, functionalized, and structurally diverse (hetero)aromatic aldehydes, ketones, carboxylic acids, esters, nitriles, and amides from alcohols in excellent yields in the presence of air.

Selective reduction of carboxylic acids to aldehydes with hydrosilane: Via photoredox catalysis

Zhang, Muliang,Li, Nan,Tao, Xingyu,Ruzi, Rehanguli,Yu, Shouyun,Zhu, Chengjian

supporting information, p. 10228 - 10231 (2017/09/22)

The direct reduction of carboxylic acids to aldehydes with hydrosilane was achieved through visible light photoredox catalysis. The combination of both single electron transfer and hydrogen atom transfer steps offers a novel and convenient approach to selective reduction of carboxylic acids to aldehydes. The method also features mild conditions, high yields, broad substrate scope, and good functional group tolerance, such as alkyne, ester, ketone, amide and amine groups.

PERNASAL PREPARATIONS

-

Page 28, (2010/11/29)

A nasal preparation comprising a compound represented by the formula: wherein Ring A is an optionally substituted 5- or 6-membered aromatic heterocyclic ring, Ring B is an optionally substituted 5- or 6-membered aromatic homocyclic or heterocyclic ring, R

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 22062-53-9