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295027

Sigma-Aldrich

Boron trifluoride

≥99.5%

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About This Item

Empirical Formula (Hill Notation):
BF3
CAS Number:
Molecular Weight:
67.81
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22

vapor density

2.38 (21 °C, vs air)

Quality Level

Assay

≥99.5%

form

gas

reaction suitability

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

bp

−100 °C (lit.)

mp

−127 °C (lit.)

SMILES string

FB(F)F

InChI

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

InChI key

WTEOIRVLGSZEPR-UHFFFAOYSA-N

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Recommended products

Monel control valve Z146978 or Monel gas regulator Z562483 is recommended.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 2 Inhalation - Eye Dam. 1 - Press. Gas Compr. Gas - Skin Corr. 1A

Supplementary Hazards

Storage Class Code

2A - Gases

WGK

WGK 1

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Joseph J Topczewski et al.
The Journal of organic chemistry, 74(18), 6965-6972 (2009-08-25)
The first total synthesis of (+)-schweinfurthin B, a potent and differentially active cytotoxic agent, has been accomplished. Completion of the synthesis required just 16 steps in the longest linear sequence from commercially available vanillin. Key synthetic transformations included a Shi
The influence of the acidity of ionic liquids on catalysis.
Xinjiang Cui et al.
ChemSusChem, 3(9), 1043-1047 (2010-08-18)
T Mizuno et al.
The Journal of chemical physics, 136(7), 074305-074305 (2012-03-01)
Recoil frame photoelectron angular distributions (RFPADs) of BF(3) molecules are presented over the energy region of the shape resonance in the F 1s continuum. Time-dependent density functional theory calculations are also given to understand the shape resonance dynamics. The RFPADs
Ramanathan Rajaganesh et al.
Carbohydrate research, 345(12), 1649-1657 (2010-06-29)
BF(3).Et(2)O-catalysed O-glycosylation of 1,2,3-tri-O-acetyl-4,6-O-butylidene- and ethylidene-beta-d-glucopyranose with different aliphatic and aromatic alcohols proceeds for the most part with complete retention of anomeric configuration. Antioxidant activity of O-glycosides shows significant inhibition (IC(50) approximately 77%). 1,3-Dipolar cycloaddition of terminal alkyne derivatives of
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

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