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Benzaldehyde, 2-hydroxy-3-methoxy-, hydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51084-72-1

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51084-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51084-72-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,8 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51084-72:
(7*5)+(6*1)+(5*0)+(4*8)+(3*4)+(2*7)+(1*2)=101
101 % 10 = 1
So 51084-72-1 is a valid CAS Registry Number.

51084-72-1SDS

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 6-(hydrazinylmethylidene)-2-methoxycyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names Benzaldehyde,2-hydroxy-3-methoxy-,hydrazone

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:51084-72-1 SDS

51084-72-1Downstream Products

51084-72-1Relevant academic research and scientific papers

Synthesis and characterization of benzo-15-crown-5 ethers with appended N2O Schiff bases

Sousa, Carla,Freire, Cristina,De Castro, Baltazar

, p. 894 - 900 (2003)

New derivatives of benzo-15-crown-5 with flexible appended N2O unsymmetrical Schiff bases were prepared by a two step procedure which involves: (i) preparation of N2O Schiff bases by condensation of hydrazine with salicylaldehyde, 3-methoxysalicylaldehyde or 2-hydroxy-1-naphtaldehyde and (ii) reaction of the resulting NH2 functionalized compounds with 4′-formyl-benzo-15-crown-5.

Calix[4]arene Schiff bases-potential ligands for fluorescent studies

Mahon, Mary F.,McGinley, John,Rooney, A. Denise,Walsh, John M.D.

experimental part, p. 11058 - 11066 (2009/04/11)

A series of novel double-armed calix[4]arene derivatives incorporating imine substituents were synthesised from the Schiff-base reaction of 25,27-bis[2-[(1-formyl-2-phenyl)oxy]ethyl]-p-tert-butylcalix[4]arene (1) with the appropriate amine or hydrazone. All compounds were characterised by various spectroscopic and analytical techniques, and in three cases, by X-ray crystallographic studies. In the case of compound 2, inclusion compounds were synthesised with both m-xylene and dimethylformamide and their X-ray structures revealed these inclusion sites-between the pendant arms and in the upper cavity, respectively. In all cases, the pendant arms are bent away from each rather than adopting a face-to-face conformation.

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