Welcome to LookChem.com Sign In|Join Free


  • or


Post Buying Request

22563-90-2 Suppliers

Recommended suppliersmore

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

22563-90-2 Usage

General Description

2-methyl-2-{[(E)-phenylmethylidene]amino}propan-1-ol, also known as phenylmethylideneamine or 2-methylpropan-1-ol, is a chemical compound with the molecular formula C10H15NO. It is a clear, colorless liquid with a faint odor and is commonly used in the pharmaceutical and chemical industries. 2-methyl-2-{[(E)-phenylmethylidene]amino}propan-1-ol is an important intermediate in the synthesis of various pharmaceutical drugs and organic compounds. It is also used as a solvent in the production of perfumes, dyes, and resins. Additionally, it has applications in the production of antioxidants and stabilizers for plastics and rubber. Overall, 2-methyl-2-{[(E)-phenylmethylidene]amino}propan-1-ol is a versatile chemical compound with a wide range of industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 22563-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,6 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22563-90:
102 % 10 = 2
So 22563-90-2 is a valid CAS Registry Number.



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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017


1.1 GHS Product identifier

Product name 2-(benzylideneamino)-2-methylpropan-1-ol

1.2 Other means of identification

Product number -
Other names -

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:22563-90-2 SDS

22563-90-2Relevant articles and documents

Synthesis and antibacterial activity of aromatic and heteroaromatic amino alcohols

de Almeida, Camila G.,Reis, Samira G.,de Almeida, Angelina M.,Diniz, Claudio G.,da Silva, Vania L.,Le Hyaric, Mireille

experimental part, p. 876 - 880 (2012/06/18)

Two series of aromatic and heteroaromatic amino alcohols were synthesized from alcohols and aldehydes and evaluated for their antibacterial activities. All the octylated compounds displayed a better activity against the four bacteria tested when evaluated by the agar diffusion method and were selected for the evaluation of minimal inhibitory concentration. The best results were obtained for p-octyloxybenzyl derivatives against Staphylococcus epidermidis (minimal inhibitory concentrations = 32μm).

Improved syntheses of fluorinated tertiary butylamines

Ok, Dong,Fisher, Michael H.,Wyvratt, Matthew J.,Meinke, Peter T.

, p. 3831 - 3834 (2007/10/03)

Two new and efficient methods using cyclic sulfamidate and nitrone chemistry were developed for the synthesis of the sterically congested 1,1- dimethyl-2-fluoroethylamine (1), 2-fluoro-1-(fluoromethyl)-1-methylethylamine (2) and 2-fluoro-1,1-bis-(fluoromethyl)-ethylamine (3).

Regio- and Diastereoselectivity in the Reaction Sequence from Secondary 3-Oxa-5-hexen-1-ylamines to Bicyclic Compounds via Nitrones

Aurich, Hans Günter,Geiger, Michael,Sievers, Ulrich

, p. 1004 - 1006 (2007/10/03)

Secondary amines 2 and 8 are oxidized by hydrogen peroxide in the presence of sodium tungstate providing nitrones. It the amino function is substituted by one primary and one secondary alkyl moiety, oxidation proceeds with high regioselectivity at the primary alkyl group affording aldonitrones. Thus, compound 2b gives exclusively 3b that undergoes an intramolecular cycloaddition yielding 4b. From 2c, however, in addition to 4c nitrone 5 is formed as by-product, which affords the bridged compound 6 on heating in toluene. Oxidation of compounds 8 yields nitrones 9 which are converted to bridged compounds 10 as major products along with small amounts of regioisomers 11 at elevated temperatures. The intramolecular cycloaddition of the chiral nitrones 3b and c as well as 9b proceeds with high diastereoselectivity.

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)


What can I do for you?
Get Best Price

Get Best Price for 22563-90-2