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Merck

295027

Sigma-Aldrich

Bortrifluorid

≥99.5%

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About This Item

Empirische Formel (Hill-System):
BF3
CAS-Nummer:
Molekulargewicht:
67.81
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352106
PubChem Substanz-ID:
NACRES:
NA.22

Dampfdichte

2.38 (21 °C, vs air)

Qualitätsniveau

Assay

≥99.5%

Form

gas

Eignung der Reaktion

core: boron
reagent type: Lewis acid
reagent type: catalyst
reaction type: Polymerization Reactions

bp

−100 °C (lit.)

mp (Schmelzpunkt)

−127 °C (lit.)

SMILES String

FB(F)F

InChI

1S/BF3/c2-1(3)4

InChIKey

WTEOIRVLGSZEPR-UHFFFAOYSA-N

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Zusätzliche Gefahrenhinweise

Lagerklassenschlüssel

2A - Gases

WGK

WGK 1

Persönliche Schutzausrüstung

Faceshields, Gloves, Goggles, multi-purpose combination respirator cartridge (US)


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Nolan R Mente et al.
The Journal of organic chemistry, 73(20), 7963-7970 (2008-09-18)
The total synthesis of the natural stilbene (+)-schweinfurthin G (8) has been accomplished through a sequence based on an efficient cationic cascade cyclization. This cascade process is initiated by Lewis acid promoted ring opening of an epoxide and terminated through
Brieuc Guillerm et al.
Macromolecular rapid communications, 33(19), 1600-1612 (2012-07-05)
Polyoxazolines (POx) are increasingly being studied as polymeric building blocks due to the possibility of affording tunable properties. Additionally, as the biocompatibility and stealth behavior of POx are similar to that of poly(ethylene glycol) (PEG), it has become challenging to
Gewu Lu et al.
ACS nano, 2(11), 2342-2348 (2009-02-12)
Polythiophene (Pth) films with aligned nanotubule arrays were adhered strongly on various smooth surfaces such as glass, mica, and GaAs after drying from their wet states under ambient condition. The normal and shear dry adhesion forces of the films on
G K Surya Prakash et al.
The Journal of organic chemistry, 74(22), 8659-8668 (2009-10-30)
BF(3)-monohydrate is found to be an efficient and strong acid catalyst as well as an effective protosolvating medium suitable for the hydroxyalkylation of arenes with aromatic aldehydes. This reaction has been extended to aromatic dialdehydes, such as terephthalic dicarboxaldehyde and
Diego dos Santos Pisoni et al.
European journal of medicinal chemistry, 45(2), 526-535 (2009-12-04)
This work describes the enantioselective synthesis of a new series of terpenic chiral 9-aminotetrahydroacridine analogues. Several chiral ketones were synthesized from natural monoterpenes in an optically active form and subjected to the cyclodehydration reactions with anthranilonitrile in the presence of

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