2-C-Methyl-D-ribono-1,4-lactone - ≥95% , CAS No.492-30-8

CAS: 492-30-8 Cat. No.: C130875 Molecular Weight: 162.14 EC Number: 610-448-4

GRADE & PURITY ≥95%

Synonyms

(3R,4R,5R)-3,4-DIHYDROXY-5-(HYDROXYMETHYL)-3-METHYLOXOLAN-2-ONE | AKOS006281432 | AC8030 | W-202871 | 2-C-Methyl-D-ribono-1,4-lactone | AS-18857 | MFCD07369541 | AC-25686 | W16702 | 3,4-dihydroxy-5-(hydroxymethyl)-3-methyl-tetrahydrofuran-2-one;2-C-Methyl

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyms

(3R, 4R, 5R)-3, 4-DIHYDROXY-5-(HYDROXYMETHYL)-3-METHYLOXOLAN-2-ONE | AKOS006281432 | AC8030 | W-202871 | 2-C-Methyl-D-ribono-1, 4-lactone | AS-18857 | MFCD07369541 | AC-25686 | W16702 | 3, 4-dihydroxy-5-(hydroxymethyl)-3-methyl-tetrahydrofuran-2-one;2-C-Methyl

Specifications & Purity

≥95%

Storage

Room temperature

Shipped In

Normal

Purity

≥95%

Names and Identifiers

• Pubchem Sid: 488197747
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488197747
• Canonical Smiles: CC1(C(C(OC1=O)CO)O)O
• IUPAC Name: (3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)-3-methyloxolan-2-one
• InChIKey: WJBVKNHJSHYNHO-ZMIZWQJLSA-N
• INCHI: 1S/C6H10O5/c1-6(10)4(8)3(2-7)11-5(6)9/h3-4,7-8,10H,2H2,1H3/t3-,4-,6-/m1/s1
• Isomeric SMILES: C[C@]1([C@@H]([C@H](OC1=O)CO)O)O
• Molecular Weight: 162.14
• Reaxy-Rn: 82511
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=82511&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Lactones
      • Subclass Gamma butyrolactones

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Lactones
• Subclass: Gamma butyrolactones
• Intermediate Tree Nodes: Not available
• Direct Parent: Gamma butyrolactones
• Alternative Parents: Monosaccharides Tertiary alcohols Oxolanes Secondary alcohols Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Primary alcohols Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Gamma butyrolactone - Monosaccharide - Oxolane - Tertiary alcohol - Carboxylic acid ester - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Oxacycle - Primary alcohol - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Organic oxygen compound - Alcohol - Carbonyl group - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as gamma butyrolactones. These are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom.
• 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

Chemical and Physical Properties

• Molecular Weight: 162.140 g/mol
• XLogP3: -1.200
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 1
• Exact Mass: 162.053 Da
• Monoisotopic Mass: 162.053 Da
• Topological Polar Surface Area: 87.000 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 180.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 3
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1