13385-66-5 Usage
Uses
Used in Pharmaceutical Industry:
2-isopropyl-5,5-dimethylthiazolidine-4-carboxylic acid hydrochloride is used as a therapeutic agent for the treatment of non-alcoholic fatty liver disease and related conditions. It is administered orally in the form of tablets, working to reduce liver fat accumulation and improve liver function by promoting the breakdown and elimination of fats.
Used in Liver Health Management:
As a liver protectant, 2-isopropyl-5,5-dimethylthiazolidine-4-carboxylic acid hydrochloride is used to support liver health by providing antioxidant protection to liver cells. This helps to mitigate damage caused by oxidative stress, which is a common factor in liver-related disorders.
Used in Antioxidant Formulations:
Due to its antioxidant properties, 2-isopropyl-5,5-dimethylthiazolidine-4-carboxylic acid hydrochloride can be used in formulations designed to combat oxidative stress and support overall health. Its inclusion in such products can contribute to the maintenance of cellular integrity and the prevention of damage from reactive oxygen species.
Overall, 2-isopropyl-5,5-dimethylthiazolidine-4-carboxylic acid hydrochloride, or Adipost, is a valuable compound in the realm of liver health and disease management, offering both therapeutic and protective benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 13385-66-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,8 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13385-66:
(7*1)+(6*3)+(5*3)+(4*8)+(3*5)+(2*6)+(1*6)=105
105 % 10 = 5
So 13385-66-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO2S.ClH/c1-5(2)7-10-6(8(11)12)9(3,4)13-7;/h5-7,10H,1-4H3,(H,11,12);1H
13385-66-5Relevant academic research and scientific papers
On the Reactivity of Penicillamine and its Derivatives. Joint Reaction of Elementary Sulfur and Gaseous Ammonia with Ketones, 97
Asinger, Friedrich,Gluzek, Karl-Heinz
, p. 47 - 63 (2007/10/02)
DL-penicillamine-hydrochloride was condensed with various aldehydes (1 - 22) and ketones (23 - 28) to the corresponding 5,5-dimethyl-thiazolidine-4-carboxylic acid hydrochlorides and the free bases respectively.Their methylesters were obtained with diazomethane or methanol (29 - 35).Various 5,5-dimethyl-thiazolidine-4-carboxylic acids were formylated in position 3 (36 - 39).The reactivity of the carboxylic group was studied for 3-formyl-2,2,5,5-tetramethyl-thiazolidine-4-carboxylic acid.Substituted N-penicillaminamides were obtained for the first time (40 - 53).Also some S-alkylated penicillamines were prepared (54 - 60).By diazotation of 2,2,5,5-tetramethyl-thiazolidine-4-carbonamide or of penicillaminamide itself, 2-carbamyl-3,3-dimethyl-ethylene-sulfide was obatined. - Keywords: 3-Formyl-2,2,5,5-tetramethyl-thiazolidine-carboxylic acid amides; N-Formyl-5,5-dimethyl-thiazolidine-4-carboxylic acids; S-Alkylpenicillamines
