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· · COA & SDS available for every product · Same-day shipping on in-stock items Balaglitazone - ≥98% , Peroxisome proliferator-activated receptor gamma partial agonist, CAS No.199113-98-9, Peroxisome proliferator-activated receptor gamma partial agonist
Synonyms
DRF2593 | NN 2344 | (+-)-5-(p-((3,4-Dihydro-3-methyl-4-oxo-2-quinazolinyl)methoxy)benzyl)-2,4-thiazolidinedione | UNII-4M1609828O | DRF 2593 | DRF-2593 | AS-63961 | SB16864 | 4-tert-butyl-phenylsulphonyl chloride | NNC-61-2344 | FT-0766930 | IETKPTYAGKZLK
Shipped In
Ice chest + Ice pads
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
DRF2593 | NN 2344 | (+-)-5-(p-((3, 4-Dihydro-3-methyl-4-oxo-2-quinazolinyl)methoxy)benzyl)-2, 4-thiazolidinedione | UNII-4M1609828O | DRF 2593 | DRF-2593 | AS-63961 | SB16864 | 4-tert-butyl-phenylsulphonyl chloride | NNC-61-2344 | FT-0766930 | IETKPTYAGKZLK
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
Description:
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
PARTIAL AGONIST
Mechanism of action
Peroxisome proliferator-activated receptor gamma partial agonist
Product Properties Names and Identifiers Canonical Smiles CN1C(=NC2=CC=CC=C2C1=O)COC3=CC=C(C=C3)CC4C(=O)NC(=O)S4 IUPAC Name 5-[[4-[(3-methyl-4-oxoquinazolin-2-yl)methoxy]phenyl]methyl]-1,3-thiazolidine-2,4-dione InChIKey IETKPTYAGKZLKY-UHFFFAOYSA-N INCHI 1S/C20H17N3O4S/c1-23-17(21-15-5-3-2-4-14(15)19(23)25)11-27-13-8-6-12(7-9-13)10-16-18(24)22-20(26)28-16/h2-9,16H,10-11H2,1H3,(H,22,24,26) Isomeric SMILES CN1C(=NC2=CC=CC=C2C1=O)COC3=CC=C(C=C3)CC4C(=O)NC(=O)S4 Molecular Weight 395.43 Reaxy-Rn 11343664 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11343664&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds Class Diazanaphthalenes Subclass Benzodiazines Intermediate Tree Nodes Not available Direct Parent Quinazolines Alternative Parents Phenoxy compounds Phenol ethers Thiazolidinediones Pyrimidones Alkyl aryl ethers Heteroaromatic compounds Dicarboximides Thiocarbamic acid derivatives Lactams Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents Quinazoline - Phenoxy compound - Phenol ether - Alkyl aryl ether - Thiazolidinedione - Pyrimidone - Monocyclic benzene moiety - Benzenoid - Pyrimidine - Dicarboximide - Heteroaromatic compound - Thiazolidine - Lactam - Thiocarbamic acid derivative - Carboxylic acid derivative - Ether - Azacycle - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as quinazolines. These are compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility 25°C: DMSO Molecular Weight 395.400 g/mol XLogP3 2.700 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 5 Exact Mass 395.094 Da Monoisotopic Mass 395.094 Da Topological Polar Surface Area 113.000 Ų Heavy Atom Count 28 Formal Charge 0 Complexity 674.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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