183556-54-9 Usage
Chemical structure
The compound consists of two main components, 1,3-benzenedimethanol and 2,2'-[2,6-pyridinediylbis(methyleneoxy)]bis[5-methyl-, connected through methyleneoxy linkages.
Functional groups
The compound contains hydroxyl (-OH) groups from the 1,3-benzenedimethanol component and a pyridine ring from the 2,2'-[2,6-pyridinediylbis(methyleneoxy)]bis[5-methylcomponent.
Molecular weight
The molecular weight of the compound is approximately 385.47 g/mol.
Appearance
The compound is likely a solid, based on its molecular weight and structure.
Solubility
The compound may be soluble in organic solvents such as ethanol, methanol, or dimethyl sulfoxide (DMSO) due to the presence of the hydroxyl and pyridine functional groups.
Synthesis
The compound can be synthesized by reacting 1,3-benzenedimethanol with a suitable 2,2'-[2,6-pyridinediylbis(methyleneoxy)]bis[5-methylprecursor, such as a halogenated derivative, through a nucleophilic substitution reaction.
Applications
The compound may have potential applications in various industries, including pharmaceuticals, materials science, and biotechnology, due to its unique structure and properties.
Stability
The compound may be sensitive to heat, light, and moisture, as it contains hydroxyl and pyridine functional groups. It should be stored in a cool, dry, and dark place to maintain its stability.
Safety
As with any chemical compound, appropriate safety precautions should be taken when handling 1,3-Benzenedimethanol, 2,2'-[2,6-pyridinediylbis(methyleneoxy)]bis[5-methyl-, including the use of personal protective equipment (PPE) and proper disposal methods.
Check Digit Verification of cas no
The CAS Registry Mumber 183556-54-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,5,5 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 183556-54:
(8*1)+(7*8)+(6*3)+(5*5)+(4*5)+(3*6)+(2*5)+(1*4)=159
159 % 10 = 9
So 183556-54-9 is a valid CAS Registry Number.
183556-54-9Relevant academic research and scientific papers
Hellier, Paul C.,Bradshaw, Jerald S.,Young, J. Jolene,Zhang, Xian Xin,Izatt, Reed M.
, p. 7270 - 7275 (1996)
An achiral (3) and two chiral pyridine-based macrobicyclic clefts (4 and 5) have been prepared by treating 2,6-bis[[2′,6′-bis(bromomethyl)-4′-methylphenoxy]methyl] pyridine (2) with the appropriate achiral and chiral glycols. Starting 2 was prepared by fi
The enantiomeric recognition of chiral organic ammonium salts by chiral pyridino-macrocycles bearing aminoalcohol subunits
Ozer, Hayriye,Kocakaya, Safak Ozhan,Akgun, Abuzer,Hosgoeren, Halil,Togrul, Mahmut
experimental part, p. 1541 - 1546 (2009/11/30)
Pyridine-based macrocycles were prepared by treating 2,6-bis[[2′6′-bis(bromomethyl)-4′-methylphenoxy]methyl]pyridine 3 with the appropriate chiral aminoalcohols. The enantiomeric recognition of these macrocycles bearing aminoalcohol subunits of the pyridinocrown type ligand was evaluated for chiral organic ammonium salts by UV titration. The important differences were observed in the Ka values of (R)-Am2 and (S)-Am2 for (S,S,S)-1, (S,S,S)-2 and (S,S,S)-3 hosts, KS/KR = 5.0, KS/KR = 2.4 and KS/KR = 5.0, respectively. There seems to be a general tendency for hosts to recognise (S)-enantiomers for both Am1 and Am2.
