13385-66-5 Usage
General Description
2-isopropyl-5,5-dimethylthiazolidine-4-carboxylic acid hydrochloride, also known as Adipost, is a synthetic derivative of cysteine that acts as a lipotropic agent and liver protectant. It is commonly used in the treatment of non-alcoholic fatty liver disease and related conditions. This chemical compound works by enhancing the breakdown and elimination of fats from the liver, thereby reducing the accumulation of fat in the liver and improving liver function. It also has antioxidant properties and may help to protect liver cells from damage caused by oxidative stress. Adipost is typically administered orally in the form of tablets and is generally well-tolerated with minimal side effects. Overall, it plays a crucial role in the management of liver health and may be beneficial for individuals with liver-related disorders.
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 articles and documents
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
