Methyl (S)-(+)-3-hydroxy-2-methylpropionate - ≥98% , CAS No.80657-57-4

CAS: 80657-57-4 Cat. No.: S133601 Peso molecular: 118.13 Beilstein Registry Number: 1720830 Número EC: 676-832-9

GRADE & PURITY ≥98%

Synonyms

H0702 | STK196652 | DTXSID80436525 | MFCD02936636 | (S)-(+)-3-Hydroxy-2-methylpropionic Acid Methyl Ester | Methyl L-(+)-.beta.-hydroxyisobutyrate | EN300-85296 | (S)-3-Hydroxyisobutyric acid methyl ester | Methyl (S)-(+)-2-methyl-3-hydroxypropionate | (S

Storage

Room temperature

Shipped In

Normal

Descripción general

Methyl (S)-(+)-3-hydroxy-2-methylpropionate may be used as a starting material in the total synthesis of (+)-discodermolide, a potent antimitotic agent.

Specifications

Sinónimos

H0702 | STK196652 | DTXSID80436525 | MFCD02936636 | (S)-(+)-3-Hydroxy-2-methylpropionic Acid Methyl Ester | Methyl L-(+)-.beta.-hydroxyisobutyrate | EN300-85296 | (S)-3-Hydroxyisobutyric acid methyl ester | Methyl (S)-(+)-2-methyl-3-hydroxypropionate | (S

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504765306
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504765306
• Sonrisas canónicas: CC(CO)C(=O)OC
• IUPAC Name: methyl (2S)-3-hydroxy-2-methylpropanoate
• InChIKey: ATCCIZURPPEVIZ-BYPYZUCNSA-N
• INCHI: 1S/C5H10O3/c1-4(3-6)5(7)8-2/h4,6H,3H2,1-2H3/t4-/m0/s1
• Isómeros SMILES: C[C@@H](CO)C(=O)OC
• WGK Alemania: 3
• Peso molecular: 118.13
• Beilstein: 1720830
• Reaxy-Rn: 1720829
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1720829&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Hydroxy acids and derivatives
      • Subclass Beta hydroxy acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Hydroxy acids and derivatives
• Subclass: Beta hydroxy acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Beta hydroxy acids and derivatives
• Alternative Parents: Methyl esters Monocarboxylic acids and derivatives Primary alcohols Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Beta-hydroxy acid - Methyl ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as beta hydroxy acids and derivatives. These are compounds containing a carboxylic acid substituted with a hydroxyl group on the C3 carbon 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

Propiedades químicas y físicas

• Índice de refracción: 1.425
• Rotación específica [α]: [α]19/D +26°, c = 4 in methanol
• Punto de inflamación (°F): 176 °F
• Punto de inflamación (°C): 81°C
• Punto de ebullición (°C): 74 °C
• Peso molecular: 118.130 g/mol
• XLogP3: -0.100
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 118.063 Da
• Monoisotopic Mass: 118.063 Da
• Topological Polar Surface Area: 46.500 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 79.700
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• 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