Borane dimethyl sulfide complex - 5.0 M in diethyl ether , CAS No.13292-87-0

CAS: 13292-87-0 Cat. No.: B130055 Formula: (CH₃)₂S·BH₃ Peso molecolare: 75.97 Beilstein Registry Number: 3663489 Numero EC: 236-313-6

QUALITÀ & PUREZZA 5.0 M in diethyl ether

Synonyms

Dimethyl sulfide borane | (Dimethyl sulfide)trihydroboron | borane Me2S | BMS | borane DMS | borane methylsulfide | borane dimethyl sulfide | borane dimethylsulfide | DMS Borane | Borane-dimethyl sulfide | boron;methylsulfanylmethane | MFCD00013189

Storage

Store at 2-8°C,Protected from light,Argon charged

Shipped In

Wet ice

Panoramica

Borane dimethyl sulfide complex is a stable source of borane used in hydroboration reduction reactions in organic synthesis. Studies indicate that Borane dimethyl sulfide complex can selectively suppress &alpha-hydroxyesters.
Usually used as a regioselective reducing agent,involved in hydroboration / oxidation and synthesis of cage compounds.

Specifiche

Sinonimi

Dimethyl sulfide borane | (Dimethyl sulfide)trihydroboron | borane Me2S | BMS | borane DMS | borane methylsulfide | borane dimethyl sulfide | borane dimethylsulfide | DMS Borane | Borane-dimethyl sulfide | boron;methylsulfanylmethane | MFCD00013189

Specifiche e purezza

5.0 M in diethyl ether

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Protected from light,Argon charged

Spedito in

Wet ice

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Nomi e identificatori

Pubchem Sid

508815461

Sorrisi canonici

[B].CSC

InChIKey

MCQRPQCQMGVWIQ-UHFFFAOYSA-N

INCHI

1S/C2H6S.B/c1-3-2;/h1-2H3;

Isomeri SMILES

[B].CSC

WGK Germania

3

Peso molecolare

75.97

Beilstein

3663489

Reaxy-Rn

14759666

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=14759666&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic salts
    • Classe Organic metal salts
      • Subclass Organic metalloid salts

• Kingdom: Organic compounds
• Superclass: Organic salts
• Classe: Organic metal salts
• Subclass: Organic metalloid salts
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic metalloid salts
• Alternative Parents: Sulfenyl compounds Dialkylthioethers Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organic metalloid salt - Dialkylthioether - Sulfenyl compound - Thioether - Hydrocarbon derivative - Organosulfur compound - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as organic metalloid salts. These are organic salt compounds containing a metalloid atom in its ionic form.
• 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

Proprietà chimiche e fisiche

• Sensibilità: Heat,Light,Air,Moisture sensitive.
• Punto di infiammabilità (°F): -31 °F
• Punto di infiammabilità (°C): -35 °C
• Peso molecolare: 72.950 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 73.0283 Da
• Monoisotopic Mass: 73.0283 Da
• Topological Polar Surface Area: 25.300 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 2.800
• 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: 2

XLogP3