Triethylborane solution - 2.0 M in diethyl ether , CAS No.97-94-9

CAS: 97-94-9 Cat. No.: T434625 Formula: C₆H₁₅B Molecular Weight: 97.99 Beilstein Registry Number: 1731462 EC Number: 202-620-9

GRADE & PURITY 2.0 M in diethyl ether

Synonyms

Boron triethyl | Triethylborane | triethyl-borane | InChI=1/C6H15B/c1-4-7(5-2)6-3/h4-6H2,1-3H | FT-0655589 | Borane, triethyl- | EN300-35961 | triethyl borane | triethylboran | Triethylborine | 4-04-00-04359 (Beilstein Handbook Reference) | BEt3 | Et3B |

Storage

Room temperature

Shipped In

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Overview

Application

Catalyst for: Allylation of aldehydes Decarboxylative C-C bond cleavage reactions Rhenium hydride / boron Lewis acid cocatalysis of alkene hydrogenations Regioselective hydroxyalkylation of unsaturated oxime ethers Reactant for radical reductions of alkyl bromides with N -heterocyclic carbene boranes Reactant for synthesis of tetramethylammonium trialkylphenylborate salts with oxidation potential

Specifications

Synonyms

Boron triethyl | Triethylborane | triethyl-borane | InChI=1/C6H15B/c1-4-7(5-2)6-3/h4-6H2,1-3H | FT-0655589 | Borane, triethyl- | EN300-35961 | triethyl borane | triethylboran | Triethylborine | 4-04-00-04359 (Beilstein Handbook Reference) | BEt3 | Et3B |

Specifications & Purity

2.0 M in diethyl ether

Storage

Room temperature

Shipped In

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Names and Identifiers

Canonical Smiles

B(CC)(CC)CC

IUPAC Name

triethylborane

InChIKey

LALRXNPLTWZJIJ-UHFFFAOYSA-N

INCHI

1S/C6H15B/c1-4-7(5-2)6-3/h4-6H2,1-3H3

Isomeric SMILES

B(CC)(CC)CC

WGK Germany

3

RTECS

ED2100000

UN Number

2845

Molecular Weight

97.99

Beilstein

1731462

Reaxy-Rn

1731462

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Class Organometalloid compounds
      • Subclass Organoboron compounds
        • Level5 Alkylboranes
          • Level6 Trialkylboranes

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Class: Organometalloid compounds
• Subclass: Organoboron compounds
• Intermediate Tree Nodes: Alkylboranes
• Direct Parent: Trialkylboranes
• Alternative Parents: Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Trialkylborane - Hydrocarbon derivative - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as trialkylboranes. These are organoboron compounds where the boron atom is substituted by only three alkyl groups.
• 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

Chemical and Physical Properties

• x_flash_point_drop_fahrenheit: -32.8 °F
• x_flash_point_drop_centigrade: -36 °C
• x_boil_point_char: 95°C
• x_melt_point_char: -92°C
• Molecular Weight: 98.000 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 3
• Exact Mass: 98.1267 Da
• Monoisotopic Mass: 98.1267 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 25.700
• 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

XLogP3

Frequently Asked Questions

How should this product be stored?

Store at room temperature.

How is this product shipped?

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What are the CAS number, molecular formula and molecular weight?

The CAS Number is 97-94-9, the molecular formula is C6H15B, and the molecular weight is 97.99 g/mol. InChIKey LALRXNPLTWZJIJ-UHFFFAOYSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.