DL-Methioninol - ≥95% , CAS No.16720-80-2

CAS: 16720-80-2 Cat. No.: S167794 Summenformel: C₅H₁₃NOS Molekulargewicht: 135.23

GRADE & PURITY ≥95%

Synonyms

2-amino-4-(methylsulfanyl)butan-1-ol | AS-44289 | BBL021540 | DL-Methioninol, >=95%, viscous liquid | METHIONINOL, DL- | WLN: L66TJ | NSC67800 | NSC-67800 | DL-Met-OL | NCIOpen2_000929 | NSC 67800 | 2-Amino-4-(methylthio)-1-butanol | DTXSID20951606 | BP-1

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Synonyme

2-amino-4-(methylsulfanyl)butan-1-ol | AS-44289 | BBL021540 | DL-Methioninol, >=95%, viscous liquid | METHIONINOL, DL- | WLN: L66TJ | NSC67800 | NSC-67800 | DL-Met-OL | NCIOpen2_000929 | NSC 67800 | 2-Amino-4-(methylthio)-1-butanol | DTXSID20951606 | BP-1

Spezifikationen & Reinheit

≥95%

Biochemische und physiologische Mechanismen

Methioninol is a methionine derivative that has been shown to inhibit SDK and TREK-1 channels in COS cells. 参考sigma

Storage

Store at 2-8°C

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥95%

Namen und Kennungen

• Pubchem Sid: 504756539
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504756539
• Kanonisches Lächeln: CSCCC(CO)N
• IUPAC Name: 2-amino-4-methylsulfanylbutan-1-ol
• InChIKey: MIQJGZAEWQQAPN-UHFFFAOYSA-N
• INCHI: 1S/C5H13NOS/c1-8-3-2-5(6)4-7/h5,7H,2-4,6H2,1H3
• Isomere SMILES: CSCCC(CO)N
• Alternative CAS-Nummer: 502-83-0
• Molekulargewicht: 135.23
• Reaxy-Rn: 1719514
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1719514&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Klasse Organonitrogen compounds
      • Subclass Amines
        • Ebene5 Alkanolamines
          • Ebene6 1,2-aminoalcohols

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Klasse: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Alkanolamines
• Direct Parent: 1,2-aminoalcohols
• Alternative Parents: Sulfenyl compounds Dialkylthioethers Primary alcohols Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: 1,2-aminoalcohol - Dialkylthioether - Sulfenyl compound - Thioether - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary alcohol - Organosulfur compound - Organooxygen compound - Primary aliphatic amine - Alcohol - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as 1,2-aminoalcohols. These are organic compounds containing an alkyl chain with an amine group bound to the C1 atom and an alcohol group bound to the C2 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

Chemische und physikalische Eigenschaften

• Molekulargewicht: 135.230 g/mol
• XLogP3: -0.300
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 135.072 Da
• Monoisotopic Mass: 135.072 Da
• Topological Polar Surface Area: 71.600 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 51.700
• 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