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Triphenylbismuth Difluoride, also known as BiPh3F2, is a chemical compound characterized by three phenyl groups bonded to a single bismuth atom, with two fluoride ions attached to the bismuth. It is a white solid with low solubility in water and is recognized for its catalytic properties in various organic reactions.

2023-48-5

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2023-48-5 Usage

Uses

Used in Organic Synthesis:
Triphenylbismuth Difluoride is used as a catalyst for facilitating a wide range of organic reactions, including carbon-carbon bond formation and other transformations. Its ability to catalyze these reactions makes it a valuable tool in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
Triphenylbismuth Difluoride is used as a potential therapeutic agent, particularly in the treatment of cancer. Its unique chemical structure and reactivity may offer new avenues for the development of anticancer drugs.
Used in Antimicrobial Applications:
Triphenylbismuth Difluoride is used as an antimicrobial agent, demonstrating potential in the development of new treatments for bacterial infections. Its ability to target and disrupt microbial processes could lead to the creation of novel antimicrobial therapies.
Used in Materials Science:
Triphenylbismuth Difluoride is used in the development of new polymers and other advanced materials. Its unique properties and reactivity may contribute to the creation of innovative materials with improved performance characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2023-48-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,2 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2023-48:
(6*2)+(5*0)+(4*2)+(3*3)+(2*4)+(1*8)=45
45 % 10 = 5
So 2023-48-5 is a valid CAS Registry Number.
InChI:InChI=1/3C6H5.Bi.2FH/c3*1-2-4-6-5-3-1;;;/h3*1-5H;;2*1H/q;;;+2;;/p-2/rC18H15BiF2/c20-19(21,16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H

2023-48-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name difluoro(triphenyl)bismuth

1.2 Other means of identification

Product number -
Other names Difluorotriphenylbismuth

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2023-48-5 SDS

2023-48-5Relevant academic research and scientific papers

The use of hexafluoropropene oxide in substitutive fluorination of Sbv and Biv oxygen-containing compounds

Lermontov,Rakov,Zefirov

, p. 1609 - 1611 (1998)

Reactions of hexafluoropropene oxide with SbV and BiV oxygen-containing compounds were studied. The E=O (E-O) groups were found to be transformed into the EF2 (E-F) (E = Sb or Bi) groups.

Synthesis and structure of triphenylbismuth difluoride

Sharutin,Sharutina,Egorova,Ivanenko,Bel'skii

, p. 44 - 45 (2007/10/03)

The reaction of triphenylbismuth dichloride with sodium fluoride in acetone leads to formation of triphenylbismuth difluoride in 73% yield. The X-ray diffraction data show that the bismuth atom in the two symmetrically independent molecules of bismuth dif

Reactions of triarylbismuth bis(arenesulfonates)

Sharutin,Sharutina,Egorova,Ettenko

, p. 1236 - 1237 (2007/10/03)

Reactions of triphenylbismuth with sodium salts, acids, alkalies, and zinc are studied. In the first three cases Bi-O bond cleavage takes place, while zinc reduces the starting bismuth compounds to triphenylbismuth.

Unexpected Formation of Triarylbismuth Diformates in the Oxidation of Triarylbismuthines with Ozone at Low Temperatures

Suzuki, Hitomi,Ikegami, Tohru,Matano, Yoshihiro,Azuma, Nagao

, p. 2411 - 2416 (2007/10/02)

Oxidation of triphenylbismuthine 1 with ozone in toluene at -78 deg C gave, unexpectedly, a high yield of triphenylbismuth diformate 3, which was also obtainable as a minor product by a similar oxidation in ethyl acetate and acetone.An X-ray crystallographic study revealed that compound 3 has C2 symmetry, the geometry around the bismuth atom being best described as a distorted trigonal bipyramid as a result of strong intramolecular interaction between the bismuth and carbonyl oxygen atoms.Treatment of compound 3 with aqueous sodium acetate or halides readily converted it into the corresponding triphenylbismuth diacetate 5 or dihalides 7 - 9.

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