55878-44-9

Basic information

• Product Name: (R)-2,2-DIMETHYL-3-FORMYL 4-THIAZOLIDINECARBOXYLIC ACID
• Synonyms: (R)-2,2-DIMETHYL-3-FORMYL 4-THIAZOLIDINECARBOXYLIC ACID;(R)-3-formyl-2,2-dimethylthiazolidine-4-carboxylic acid
• CAS NO: 55878-44-9
• Molecular Formula: C₇H₁₁NO₃S
• Molecular Weight: 189.23
• Mol File: 55878-44-9.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (R)-2,2-DIMETHYL-3-FORMYL 4-THIAZOLIDINECARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2,2-DIMETHYL-3-FORMYL 4-THIAZOLIDINECARBOXYLIC ACID(55878-44-9)
• EPA Substance Registry System: (R)-2,2-DIMETHYL-3-FORMYL 4-THIAZOLIDINECARBOXYLIC ACID(55878-44-9)

Safety Data

• Hazardous Substances Data: 55878-44-9(Hazardous Substances Data)

Usage

Description

(R)-2,2-DIMETHYL-3-FORMYL 4-THIAZOLIDINECARBOXYLIC ACID is a thiazolidinecarboxylic acid derivative with the molecular formula C7H11NO3S. It is a chiral molecule, which means it has two mirror-image forms, with the (R)-enantiomer being the biologically active one. (R)-2,2-DIMETHYL-3-FORMYL 4-THIAZOLIDINECARBOXYLIC ACID has potential pharmaceutical applications due to its ability to inhibit the dipeptidyl peptidase 4 (DPP-4) enzyme activity.

Uses

Used in Pharmaceutical Industry:
(R)-2,2-DIMETHYL-3-FORMYL 4-THIAZOLIDINECARBOXYLIC ACID is used as a DPP-4 inhibitor for the treatment of type 2 diabetes. It helps regulate blood sugar levels by increasing the concentration of incretin hormones, which in turn improves glycemic control and reduces the risk of hyperglycemia.
Additionally, due to its potential role in the development of new medications for diabetes and other metabolic disorders, (R)-2,2-DIMETHYL-3-FORMYL 4-THIAZOLIDINECARBOXYLIC ACID is used as a research compound in the pharmaceutical industry. Researchers are interested in exploring its properties and potential applications in the development of innovative treatments for various metabolic conditions.

Upstream product

• 141-53-7 sodium formate 
• 67089-92-3 L-(-)-2,2-dimethylthiazolidine-4-carboxylic acid hydrochloride salt 
• 58166-38-4 2,2-dimethyl-thiazolidine-4(R)-carboxylic acid 
• 64-18-6 formic acid 

Downstream Products

• 100616-25-9 N,S-diacetyl-L-cysteine anilide 
• 74527-65-4 N-((R)-3-formyl-2,2-dimethyl-thiazolidine-4-carbonyl)-glycine 
• 134020-10-3 3-Formyl-2,2-dimethyl-thiazolidine-4-carboxylic acid (2R,3S,5R)-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-2-trityloxymethyl-tetrahydro-furan-3-yl ester 
• 1334521-74-2 (1R,5R)-6-(benzyloxy)-3,3-dimethyl-7-oxo-4-thia-2,6-diazabicyclo[3.2.0]heptane-2-carboxaldehyde 
• 1334521-60-6 (4R,5S)-N-benzyloxy-3-formyl-5-hydroxy-2,2-dimethylthiazolidine-4-carboxamide 
• 101715-73-5 (R)-3-formyl-2,2-dimethyl-thiazolidine-4-carboxylic acid-(4-pentyloxy-anilide) 
• 100706-07-8 (R)-3-formyl-2,2-dimethyl-thiazolidine-4-carboxylic acid-(N'-phenyl-hydrazide) 
• 81355-92-2 (R)-3-formyl-2,2-dimethyl-thiazolidine-4-carboxylic acid anilide 
• 99167-92-7 (+/-)-N-(3-formyl-2,2-dimethyl-thiazolidine-4-carbonyl)-glycine-methyl ester 

Relevant articles and documents

Decoration of Au and Ag nanoparticles on self-assembling pseudopeptide-based nanofiber by using a short peptide as capping agent for metal nanoparticles

The surface of a nanofiber that is formed from a self-assembling pseudopeptlde has been decorated by gold and silver nanoparticles that are stabilized by a dipeptide. Transmission electron microscopic images make the decoration visible. In this paper, a new strategy of mineralizing a pseudopeptide based nanofiber by gold and silver nanoparticles with use of a two-component nanografting method is described.