13206-31-0 Usage
Description
2-Isopropyl-5,5-dimethylthiazolidine-4-carboxylic acid, also known as 5,5-dimethyl-2-(1-methylethyl)-4-thiazolidinecarboxylic acid, is a penicillamine analogue with a unique chemical structure that exhibits various therapeutic properties. It is characterized by its ability to chelate metals and modulate immune responses, making it a versatile compound with potential applications in the medical field.
Uses
Used in Pharmaceutical Industry:
2-Isopropyl-5,5-dimethylthiazolidine-4-carboxylic acid is used as a therapeutic agent for the treatment of various medical conditions, including arthritis, kidney stones, and metal poisoning. Its chelating properties enable it to bind and remove excess metals from the body, while its immunomodulatory effects help alleviate the symptoms of arthritis and other autoimmune disorders.
Used in Arthritis Treatment:
In the treatment of arthritis, 2-isopropyl-5,5-dimethylthiazolidine-4-carboxylic acid acts as an anti-inflammatory and immunomodulatory agent, reducing inflammation and pain associated with the condition. It helps to regulate the immune system's response, which can be beneficial for patients suffering from autoimmune arthritis.
Used in Kidney Stone Treatment:
For kidney stones, 2-isopropyl-5,5-dimethylthiazolidine-4-carboxylic acid functions as a chelating agent, binding to and facilitating the excretion of excess minerals and metals that contribute to the formation of kidney stones. This can help to prevent the recurrence of kidney stones and alleviate associated symptoms.
Used in Metal Poisoning Treatment:
In cases of metal poisoning, 2-isopropyl-5,5-dimethylthiazolidine-4-carboxylic acid is used as a detoxifying agent. Its ability to chelate and remove toxic metals from the body makes it an effective treatment for heavy metal poisoning, such as lead, mercury, or cadmium intoxication.
Check Digit Verification of cas no
The CAS Registry Mumber 13206-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,0 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13206-31:
(7*1)+(6*3)+(5*2)+(4*0)+(3*6)+(2*3)+(1*1)=60
60 % 10 = 0
So 13206-31-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO2S/c1-5(2)7-10-6(8(11)12)9(3,4)13-7/h5-7,10H,1-4H3,(H,11,12)
13206-31-0Relevant 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
