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Key Documents

901267

Sigma-Aldrich

Hexamethylborazine

≥95%

Synonym(s):

1,2,3,4,5,6-Hexamethyl-1,3,5,2,4,6-triazatriborinane

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About This Item

Empirical Formula (Hill Notation):
C6H18B3N3
CAS Number:
Molecular Weight:
164.66
MDL number:
UNSPSC Code:
12352200

Quality Level

Assay

≥95%

form

powder or crystals

reaction suitability

core: boron
reagent type: catalyst

mp

99 °C

storage temp.

−20°C

InChI

1S/C6H18B3N3/c1-7-10(4)8(2)12(6)9(3)11(7)5/h1-6H3

InChI key

LCHQMXUQYONIOI-UHFFFAOYSA-N

Application

Hexamethylborazine has been developed by the Szymczak lab for the delivery of alkyl and hydride nucleophiles in addition to being a key component in the synthesis of recyclable trifluoromethylation reagents.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Angewandte Chemie (International ed. in English), 51(52), 13168-13172 (2012-11-20)
Recharging spent BN fuel: {Cr(CO)(3)} mediates the reduction of borazines by hydride and methyl nucleophiles to generate anionic complexes of dearomatized hexamethylborazine. Subsequent quenching leads to the release of a substituted cyclotriborazane, successfully demonstrating the stepwise reduction of a B=N
Borazine?CF3? Adducts for Rapid, Room Temperature, and Broad Scope Trifluoromethylation.
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Reduction of Borazines Mediated by Low?Valent Chromium Species.
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Manganese-Mediated Hydride Delivery to a Borazine by Stepwise Reduction and Protonation.
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Anna S Lisovenko et al.
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Donor-acceptor complexes of borazine (BZ) and its substituted derivatives with Lewis acids (A = MCl(3), MBr(3); M = B, Al, Ga) and Lewis bases (D = NH(3), Py) have been theoretically studied at the B3LYP/TZVP level of theory. The calculations

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