Methyl-β-D-thiogalactoside - ≥98% , CAS No.155-30-6

CAS: 155-30-6 Cat. No.: M120901 Formula: C₇H₁₄O₅S Peso molecolare: 210.25 Beilstein Registry Number: 81583 Numero EC: 205-842-4

GRADE & PURITY ≥98%

Synonyms

(2R,3R,4S,5R,6S)-2-(Hydroxymethyl)-6-(methylthio)tetrahydro-2H-pyran-3,4,5-triol | LZFNFLTVAMOOPJ-PZRMXXKTSA-N | Methyl- | DTXSID20883337 | NSC 19048 | B-D-Thiomethylgalactoside | EX-A922 | E84872 | AKOS027430434 | Methyl-1-thio-b-D-galactoside | SCHEMBL2

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Specifications

Sinonimi

(2R,3R,4S,5R,6S)-2-(Hydroxymethyl)-6-(methylthio)tetrahydro-2H-pyran-3,4,5-triol | LZFNFLTVAMOOPJ-PZRMXXKTSA-N | Methyl- | DTXSID20883337 | NSC 19048 | B-D-Thiomethylgalactoside | EX-A922 | E84872 | AKOS027430434 | Methyl-1-thio-b-D-galactoside | SCHEMBL2

Specifiche e purezza

≥98%

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥98%

Nomi e identificatori

• Pubchem Sid: 528773425
• Sorrisi canonici: CSC1C(C(C(C(O1)CO)O)O)O
• IUPAC Name: (2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-methylsulfanyloxane-3,4,5-triol
• InChIKey: LZFNFLTVAMOOPJ-PZRMXXKTSA-N
• INCHI: 1S/C7H14O5S/c1-13-7-6(11)5(10)4(9)3(2-8)12-7/h3-11H,2H2,1H3/t3-,4+,5+,6-,7+/m1/s1
• Isomeri SMILES: CS[C@H]1[C@@H]([C@H]([C@H]([C@H](O1)CO)O)O)O
• WGK Germania: 3
• Peso molecolare: 210.25
• Beilstein: 81583
• Reaxy-Rn: 25226617
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=25226617&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Glycosyl compounds
          • Level6 Thioglycosides

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Glycosyl compounds
• Direct Parent: Thioglycosides
• Alternative Parents: Oxanes Monosaccharides Monothioacetals Secondary alcohols Sulfenyl compounds Polyols Oxacyclic compounds Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: S-glycosyl compound - Oxane - Monosaccharide - Monothioacetal - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Sulfenyl compound - Polyol - Hydrocarbon derivative - Primary alcohol - Organosulfur compound - Alcohol - Aliphatic heteromonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as thioglycosides. These are glycoside in which a sugar group is bonded through one carbon to another group via a S-glycosidic bond.
• 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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Peso molecolare: 210.250 g/mol
• XLogP3: -1.300
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• Exact Mass: 210.056 Da
• Monoisotopic Mass: 210.056 Da
• Topological Polar Surface Area: 115.000 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 167.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 5
• 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