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Diphenylbismuthanyl-acetic acid (1:1) is a chemical compound with the formula C14H13BiO2. It is a derivative of acetic acid, where one of the hydrogen atoms is replaced by a diphenylbismuthanyl group. diphenylbismuthanyl - acetic acid (1:1) is characterized by the presence of a bismuth atom bonded to two phenyl rings, which gives it unique chemical properties. It is often used in organic synthesis and as a reagent in various chemical reactions due to its ability to act as a Lewis acid. The 1:1 ratio in the name indicates that one molecule of diphenylbismuthanyl is combined with one molecule of acetic acid. diphenylbismuthanyl - acetic acid (1:1) is of interest in the field of organometallic chemistry and has potential applications in the development of new materials and catalysts.

4723-24-4

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4723-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4723-24-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,2 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4723-24:
(6*4)+(5*7)+(4*2)+(3*3)+(2*2)+(1*4)=84
84 % 10 = 4
So 4723-24-4 is a valid CAS Registry Number.

4723-24-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Bismuthine, (acetyloxy)diphenyl-

1.2 Other means of identification

Product number -
Other names Silane,diphenylbis(phenylthio)

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:4723-24-4 SDS

4723-24-4Relevant academic research and scientific papers

Synthesis and reactivity of chiral pentavalent bismuth derivatives

Finet,Fedorov

, p. 1488 - 1495 (2007/10/03)

Eight new pentavalent organobismuth derivatives were synthesized by the reactions of triphenylbismuth or phenyl-2,2"-biphenylenebismuth with chiral (1R)-(-)-camphor-10-sulfonic, (-)-menthyloxyacetic, or (R)-3-phenylbutyric acids. Enantioselective C-arylat

Observations on the Cleavage of the Bismuth-carbon bond in BiV Compounds: a New Arylation Reaction

Barton, Derek H. R.,Lester, David J.,Motherwell, William B.,Papoula, M. Teresa Barros

, p. 246 - 247 (2007/10/02)

Further examples of the selectivity of pentavalent triaryl-organobismuth oxidants are presented; deuterium labelling studies have established that the mechanism of oxidation of allylic alcohols by these reagents involves, to some extent, cleavage of the bismuth-aryl bond; several reactions involving the synthetically useful transfer of an aryl group from bismuth to nitrogen and to carbon are described.

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