113231-34-8 Usage
Molecular weight
390.46 g/mol
Structure
2,6-Pyridinedicarboxaldehyde, 3-(phenylmethoxy)-, bis(methyl-2-pyridinylhydrazone) is a derivative of 2,6-Pyridinedicarboxaldehyde with two methyl-2-pyridinylhydrazone groups and a phenylmethoxy group attached to it.
Appearance
It is a solid with a brown or yellowish-brown color.
Solubility
It is soluble in common organic solvents such as DMSO, ethanol, and methanol.
Reactivity
The presence of the aldehyde and hydrazone groups in the molecule makes it reactive and capable of undergoing various chemical reactions such as condensation, reduction, and cyclization.
Uses
It is used in organic synthesis and pharmaceutical research as a building block for the preparation of various organic compounds. The addition of the phenylmethoxy group imparts specific properties to the compound, making it useful in the development of new drugs and materials. The two pyridinylhydrazone groups increase its stability and allow for multiple applications in chemical reactions and biological assays.
Safety
It should be handled with care as it can be harmful if ingested, inhaled, or absorbed through the skin. It should be stored in a cool, dry place and kept away from sources of ignition or oxidizing agents.
Check Digit Verification of cas no
The CAS Registry Mumber 113231-34-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,2,3 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113231-34:
(8*1)+(7*1)+(6*3)+(5*2)+(4*3)+(3*1)+(2*3)+(1*4)=68
68 % 10 = 8
So 113231-34-8 is a valid CAS Registry Number.
113231-34-8Relevant articles and documents
Synthesis of 2,6-Diformyl-3-hydroxypyridine Bis: A Pentadentate N,N,N,N,N Ligand for the Preparation of Chelating Resins
Baldo, Maria Antonietta,Chessa, Gavino,Marangoni, Giampaolo,Pitteri, Bruno
, p. 720 - 723 (2007/10/02)
The synthesis of 2,6-diformyl-3-hydroxypyridine bis as a versatile intermediate with a reactive hydroxyl group, which can be bonded to lipophilic chains and/or to polymeric supports, is reported.
