18455-58-8 Usage
General Description
2,5,5-trimethyl-1,3-thiazolidine-4-carboxylic acid is a compound that belongs to the thiazolidine family. It is a derivative of thiazolidine-4-carboxylic acid, and its chemical structure includes a thiazolidine ring with three methyl groups attached to the carbon atom at positions 2, 5, and 5. 2,5,5-trimethyl-1,3-thiazolidine-4-carboxylic acid has been studied for its potential therapeutic properties, particularly in the treatment of diabetes and metabolic disorders. It has been shown to have anti-inflammatory and antioxidant effects, and it may also play a role in regulating glucose and lipid metabolism. Additionally, 2,5,5-trimethyl-1,3-thiazolidine-4-carboxylic acid has been evaluated for its potential as a food additive or supplement due to its reported health benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 18455-58-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,5 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18455-58:
(7*1)+(6*8)+(5*4)+(4*5)+(3*5)+(2*5)+(1*8)=128
128 % 10 = 8
So 18455-58-8 is a valid CAS Registry Number.
18455-58-8Relevant articles and documents
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Nagasawa et al.
, p. 1274,1277 (1978)
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Chemistry of diazafulvenium methides in the synthesis of functionalized pyrazoles
Pinho E Melo, Teresa M. V. D.,Nunes, Claudio M.,Soares, Maria I. L.,Paixao, Jose A.,Beja, Ana Matos,Silva, Manuela Ramos
, p. 4406 - 4415 (2008/02/05)
(Chemical Equation Presented) The chemistry of diazafulvenium methides generated by the thermal extrusion of sulfur dioxide from 2,2-dioxo-1H,3H- pyrazolo[1,5-c] [1,3]thiazoles is described. The diazafulvenium methides unsubstituted at C-7 participate in [8π + 2π] cycloadditions giving pyrazolo-annulated heterocycles resulting from the addition across the 1,7-position. 1-Mefhyl-diazafulvenium methides and 7,7-dimethyl-diazafulvenium methides undergo intramolecular sigmatropic [1,8]H shifts giving vinyl- 1H-pyrazoles.
