Welcome to LookChem.com Sign In|Join Free
  • or
Benzenemethanol, a-[[[(2-hydroxyphenyl)methylene]amino]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67492-08-4

Post Buying Request

67492-08-4 Suppliers

Recommended suppliers

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

67492-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67492-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,4,9 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67492-08:
(7*6)+(6*7)+(5*4)+(4*9)+(3*2)+(2*0)+(1*8)=154
154 % 10 = 4
So 67492-08-4 is a valid CAS Registry Number.

67492-08-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(<(2-hydroxy-2-phenylethyl)imino>methyl)phenol

1.2 Other means of identification

Product number -
Other names 2-{[(E)-2-Hydroxy-2-phenyl-ethylimino]-methyl}-phenol

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:67492-08-4 SDS

67492-08-4Downstream Products

67492-08-4Relevant academic research and scientific papers

Ligand Exchange Chromatography of Amino Alcohols. Use of Schiff Bases in Enantiomer Resolution

Gelber, Loren R.,Karger, Barry L.,Neumeyer, John L.,Feibush, Binyamin

, p. 7729 - 7734 (1984)

A new method for enantiomeric resolution of primary amino alcohols by HPLC is described involving derivatization to the salicylaldehyde Schiff base followed by ligand exchange chromatography (LEC) with chiral L-proline-bonded stationary phases.All of the α-amino alcohols with a hydroxyl substituent on the asymmetric carbon examined were resolved, including catecholamines and other β-hydroxyphenethylamines.The copper(II) ion employed in LEC serves to stabilize the Schiff base, whereas the derivative permits complexation in a manner favorable for resolution and enhanced detection.A possible structure for the mixed complex responsible for separation is suggested.From this structure, a correlation between elution order and configuration is proposed.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 67492-08-4