2-Mercaptoethanol - BioReagent , CAS No.60-24-2

CAS: 60-24-2 Cat. No.: M274256 Formula: C₂H₆OS Peso molecolare: 78.13 Beilstein Registry Number: 773648 Numero EC: 200-464-6

QUALITÀ & PUREZZA BioReagent

Synonyms

2-mercaptoethanol|Mercaptoethanol|60-24-2|Beta-Mercaptoethanol|Thioglycol|2-Sulfanylethanol|Ethanol, 2-mercapto-|2-Thioethanol|Thioethylene glycol|2-Hydroxyethanethiol|2-Hydroxyethyl mercaptan|Monothioglycol|Thiomonoglycol|2-Hydroxy-1-ethanethiol|1-Ethano

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Specifiche

Sinonimi

2-mercaptoethanol | Mercaptoethanol | 60-24-2 | Beta-Mercaptoethanol | Thioglycol | 2-Sulfanylethanol | Ethanol, 2-mercapto- | 2-Thioethanol | Thioethylene glycol | 2-Hydroxyethanethiol | 2-Hydroxyethyl mercaptan | Monothioglycol | Thiomonoglycol | 2-Hydroxy-1-ethanethiol | 1-Ethano

Specifiche e purezza

BioReagent

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged

Spedito in

FedEx DG Service

Grado

BioReagent

Nomi e identificatori

Pubchem Sid

508813351

Sorrisi canonici

C(CS)O

IUPAC Name

2-sulfanylethanol

InChIKey

DGVVWUTYPXICAM-UHFFFAOYSA-N

INCHI

1S/C2H6OS/c3-1-2-4/h3-4H,1-2H2

Isomeri SMILES

C(CS)O

WGK Germania

3

RTECS

KL5600000

Numero UN

UN 2966

Gruppo di imballaggio

II

Peso molecolare

78.13

Beilstein

773648

Reaxy-Rn

773648

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=773648&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organosulfur compounds
    • Classe Thiols
      • Subclass Alkylthiols

• Kingdom: Organic compounds
• Superclass: Organosulfur compounds
• Classe: Thiols
• Subclass: Alkylthiols
• Intermediate Tree Nodes: Not available
• Direct Parent: Alkylthiols
• Alternative Parents: Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alkylthiol - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as alkylthiols. These are organic compounds containing the thiol functional group linked to an alkyl chain.
• External Descriptors: a small molecule

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

Obiettivi associati (umani)

CA2 Tclin Carbonic anhydrase II (17698 Activities)

Discover Target: CA2

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

CA9 Tclin Carbonic anhydrase IX (8255 Activities)

Discover Target: CA9

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Sensibilità: Moisture Sensitive & Air Sensitive
• Indice di rifrazione: 1.499-1.502
• Punto di infiammabilità (°F): 167℉
• Punto di infiammabilità (°C): 75℃
• Punto di ebollizione (°C): 157-158°C
• Punto di fusione (°C): -100°C
• Peso molecolare: 78.140 g/mol
• XLogP3: -0.200
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 78.0139 Da
• Monoisotopic Mass: 78.0139 Da
• Topological Polar Surface Area: 21.200 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 10.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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