Borane - tert-Butylamine Complex - ≥95% , CAS No.7337-45-3

CAS: 7337-45-3 Cat. No.: B134008 Summenformel: BH₃·C₄H₁₁N Molekulargewicht: 86.97 EG-Nummer: 230-851-5 PubChem CID: 6364547

GRADE & PURITY ≥95%

Synonyms

borane t-butylamine | MFCD00075635 | borane-tert-butylamine | tert-butylamine-borane | FT-0623163 | J-519924 | tert-Butylamine borane | GKFJEDWZQZKYHV-UHFFFAOYSA-N | AMY14898 | B1264 | AKOS015833621 | F14004 | t-butylamine.borane | NSC 114045

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Übersicht

Borane tert-butylamine complex is a mild reducing agent. It participates in the selective reduction of aldehydes and ketones to corresponding alcohol. It takes part as a reducing agent in the synthesis of monodisperse palladium nanoparticles (Pd NPs), monodisperse gold (Au) nanoparticles and carbon-supported Pd electrocatalysts.

Specifications

Synonyme

borane t-butylamine | MFCD00075635 | borane-tert-butylamine | tert-butylamine-borane | FT-0623163 | J-519924 | tert-Butylamine borane | GKFJEDWZQZKYHV-UHFFFAOYSA-N | AMY14898 | B1264 | AKOS015833621 | F14004 | t-butylamine.borane | NSC 114045

Spezifikationen & Reinheit

≥95%

Anmeldung

Reactant involved in: Non-destructive analyses and conservation treatments of Indian drawings Dehydrogenation reactions mediated by ruthenium bidentate phosphine complexes or ruthenium / iridium bis(N-heterocyclic carbene) complexes The formation of σ-bor

Storage

Store at 2-8°C,Argon charged

Verschickt in

Wet ice

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

Reinheit

≥95%

Namen und Kennungen

• Pubchem Sid: 508814943
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/508814943
• Kanonisches Lächeln: [B].CC(C)(C)N
• InChIKey: PVYPHUYXKVVURH-UHFFFAOYSA-N
• INCHI: 1S/C4H11N.B/c1-4(2,3)5;/h5H2,1-3H3
• Isomere SMILES: [B].CC(C)(C)N
• WGK Deutschland: 3
• RTECS: EO3900000
• PubChem CID: 6364547
• Molekulargewicht: 86.97
• Reaxy-Rn: 4134905

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic salts
• Klasse: Organic metal salts
• Subclass: Organic metalloid salts
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic metalloid salts
• Alternative Parents: Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organic metalloid salt - Organic nitrogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic acyclic compound
• Beschreibung: 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

Chemische und physikalische Eigenschaften

• Löslichkeit: Soluble in water (27 mg/ml), and methanol
• Empfindlichkeit: Moisture & Heat & Air sensitive
• Schmelzpunkt (°C): 96-98°C
• Molekulargewicht: 83.950 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 84.0985 Da
• Monoisotopic Mass: 84.0985 Da
• Topological Polar Surface Area: 26.000 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 25.100
• 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

Referenzen

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