17087-36-4 Usage
Chemical Family
2-(1,2,3,4-tetrahydroxybutyl)thiazolidine-4-carboxylic acid belongs to the thiazolidine-4-carboxylic acid family.
Derivation
It is derived from butyl thiazolidine.
Molecular Structure
Characterized by a tetrahydroxybutyl group attached to the thiazolidine ring.
Pharmacological Applications
Has potential pharmacological applications due to its antioxidant and anti-inflammatory properties.
Potential Use
Studied for its potential use in the treatment of various diseases, including diabetes and cardiovascular conditions.
Chelating Agent
Investigated as a potential chelating agent for metal ions.
Building Block
Used as a building block for the synthesis of novel compounds with therapeutic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 17087-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,8 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17087-36:
(7*1)+(6*7)+(5*0)+(4*8)+(3*7)+(2*3)+(1*6)=114
114 % 10 = 4
So 17087-36-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO6S/c10-1-4(11)5(12)6(13)7-9-3(2-16-7)8(14)15/h3-7,9-13H,1-2H2,(H,14,15)
17087-36-4Relevant articles and documents
MAILLARD REACTION COMPOUNDS OF CYSTEINE AND A SUGAR HAVING MEATLIKE FLAVOUR
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Page/Page column 6, (2008/06/13)
The Amadori compounds of cysteine of Formula (I) in which R is hydrogen when n=1-4, or methyl when n=0-3. The compounds are useful for conferring meaty tastes and aromas on foodstuffs.
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.
