Tetrahydrofuran-2,3,4,5-tetracarboxylic Acid - ≥98%(T) , CAS No.26106-63-8

CAS: 26106-63-8 Cat. No.: T161756 Molecular Weight: 248.14 EC Number: 247-461-6 PubChem CID: 97421

GRADE & PURITY ≥98%(T)

Synonyms

FT-0638573 | 2,5-anhydro-3,4-dicarboxy-3,4-dideoxyhexaric acid | UFOIOXZLTXNHQH-UHFFFAOYSA-N | DTXSID60948994 | D92427 | NSC 122277 | TETRAHYDROFURAN-2,3,4,5-TETRACARBOXYLICACID | C8H8O9 | T0975 | Tetrahydrofuran-2,3,4,5-tetracarboxylic Acid | 2,3,4,5-Fur

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyms

FT-0638573 | 2, 5-anhydro-3, 4-dicarboxy-3, 4-dideoxyhexaric acid | UFOIOXZLTXNHQH-UHFFFAOYSA-N | DTXSID60948994 | D92427 | NSC 122277 | TETRAHYDROFURAN-2, 3, 4, 5-TETRACARBOXYLICACID | C8H8O9 | T0975 | Tetrahydrofuran-2, 3, 4, 5-tetracarboxylic Acid | 2, 3, 4, 5-Fur

Specifications & Purity

≥98%(T)

Storage

Room temperature

Shipped In

Normal

Purity

≥98%(T)

Names and Identifiers

• Pubchem Sid: 488187050
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488187050
• Canonical Smiles: C1(C(C(OC1C(=O)O)C(=O)O)C(=O)O)C(=O)O
• IUPAC Name: oxolane-2,3,4,5-tetracarboxylic acid
• InChIKey: UFOIOXZLTXNHQH-UHFFFAOYSA-N
• INCHI: 1S/C8H8O9/c9-5(10)1-2(6(11)12)4(8(15)16)17-3(1)7(13)14/h1-4H,(H,9,10)(H,11,12)(H,13,14)(H,15,16)
• Isomeric SMILES: C1(C(C(OC1C(=O)O)C(=O)O)C(=O)O)C(=O)O
• PubChem CID: 97421
• Molecular Weight: 248.14
• Reaxy-Rn: 1394540

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Tetracarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Tetracarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Tetracarboxylic acids and derivatives
• Alternative Parents: Tetrahydrofurans Oxacyclic compounds Dialkyl ethers Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Tetracarboxylic acid or derivatives - Tetrahydrofuran - Oxacycle - Organoheterocyclic compound - Ether - Dialkyl ether - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups.
• 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.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

GNAS Tbio Guanine nucleotide-binding protein G(s), subunit alpha (103405 Activities)

Discover Target: GNAS

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Melt Point(°C): 205℃
• Molecular Weight: 248.140 g/mol
• XLogP3: -1.800
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 4
• Exact Mass: 248.017 Da
• Monoisotopic Mass: 248.017 Da
• Topological Polar Surface Area: 158.000 Ų
• Heavy Atom Count: 17
• Formal Charge: 0
• Complexity: 350.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 4
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1