59246-17-2 Usage
Thiazolidine derivative
A compound derived from a 1,3-thiazolidine ring, which is a five-membered heterocyclic ring system containing sulfur and nitrogen atoms.
Tetrahydroxybutyl functional group
A functional group consisting of a butyl chain (a four-carbon chain) with four hydroxyl (-OH) groups attached to the carbon atoms.
Carboxylic acid functional group
A functional group containing a carbonyl group (C=O) and a hydroxyl group (-OH), forming a carboxyl group (-COOH).
Pharmaceutical applications
The potential use of this compound in the development of medications, particularly in the treatment of diseases or medical conditions.
Anti-diabetic effects
The ability of the compound to help manage diabetes by improving insulin sensitivity and regulating blood sugar levels.
Anti-inflammatory properties
The potential of the compound to reduce inflammation, which is a response to injury or infection in the body.
Antioxidant properties
The ability of the compound to neutralize or reduce the effects of free radicals, which are unstable molecules that can cause damage to cells and contribute to various diseases.
Further research interest
The compound's potential for further investigation in the field of drug development and therapeutic applications due to its various properties and potential health benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 59246-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,2,4 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59246-17:
(7*5)+(6*9)+(5*2)+(4*4)+(3*6)+(2*1)+(1*7)=142
142 % 10 = 2
So 59246-17-2 is a valid CAS Registry Number.
59246-17-2Relevant articles and documents
Proton and Zinc(II) Complexes of 2-(Polyhydroxyalkyl)thiazolidine-4-carboxylic acid Derivatives
Gajda, Tamas,Nagy, Laszlo,Burger, Kalman
, p. 3155 - 3160 (2007/10/02)
The protonation and zinc-ion co-ordination equilibria of 2-(polyhydroxyalkyl)thiazolidine-4-carboxylic acid derivatives have been studied by potentiometric titration in the range pH 1.5-8.In most cases the formation of complexes with a metal-to-ligand ratio of 1:2 was demonstrated, but at above pH 6 mixed-ligand complexes involving hydroxide-ion co-ordination were also observed.The protonation and complex-formation constants were shown to depend on the structure of the polyhydroxy chains.In the case of the protonation constants this is due to the rearrangement of the intramolecular hydrogen-bonding network, while the complex-formation constants depend on the conformation of the OH groups on the first carbon atoms of the polyol chains.
