5153-29-7 Usage
Uses
Used in Organic Synthesis:
Tris(4-bromophenyl)bismuthane is utilized as a catalyst in organic synthesis for facilitating reactions such as cross-coupling and C-H activation. Its role in these processes is to accelerate the reaction rates and improve the overall efficiency of the synthesis.
Used in Catalyst Replacement:
tris(4-bromophenyl)bismuthane serves as an alternative to palladium-based catalysts, which are often expensive and toxic. Tris(4-bromophenyl)bismuthane offers a more sustainable and cost-effective option for industries that rely on catalysis in their chemical processes.
Used in Organic Electronics:
tris(4-bromophenyl)bismuthane has been studied for its potential applications in the field of organic electronics, where its properties may contribute to the development of new electronic materials and devices.
Used in Pharmaceuticals:
Tris(4-bromophenyl)bismuthane has been investigated for its possible use in pharmaceuticals, suggesting that it could be a component in the development of new drugs or drug delivery systems.
Used in Antimicrobial Applications:
tris(4-bromophenyl)bismuthane has demonstrated antimicrobial properties, making it a candidate for further research and development as an antibacterial agent, which could be particularly useful in environments where resistance to existing antibiotics is a concern.
Check Digit Verification of cas no
The CAS Registry Mumber 5153-29-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,5 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5153-29:
(6*5)+(5*1)+(4*5)+(3*3)+(2*2)+(1*9)=77
77 % 10 = 7
So 5153-29-7 is a valid CAS Registry Number.
5153-29-7Relevant academic research and scientific papers
DIHYDRONEPETALACTAMS AND N-SUBSTITUTED DERIVATIVES THEREOF
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Page/Page column 27, (2008/06/13)
Dihydronepetalactams and N-substituted derivatives thereof are prepared by alkylation of metallated lactams. Dihydronepetalactams and N-substituted derivatives thereof have utility as insect repellents.
Nepetalactams and N-substituted derivatives thereof
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Page/Page column 8, (2008/06/13)
Nepetalactams and N-substituted derivatives thereof are prepared by alkylation of metallated lactams. Nepetalactams and N-substituted derivatives thereof have utility as insect repellents.
Non-cluster type bismuth compounds
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, (2008/06/13)
PCT No. PCT/GB96/00183 Sec. 371 Date Oct. 22, 1997 Sec. 102(e) Date Oct. 22, 1997 PCT Filed Jan. 26, 1996 PCT Pub. No. WO96/22994 PCT Pub. Date Aug. 1, 1996A method of generating an image of a human or non-human animal body which comprises administering t
SYNTHESIS OF METALLOCHIRAL TRIORGANOBISMUTHINES
Bras, P.,Gen, A. Van Der,Wolters, J.
, p. C1 - C4 (2007/10/02)
Triorganobismuthines containing a chiral centre at the metal atom have been prepared by selective bromodearylation of mixed triarylbismuthines, followed by reaction of the resulting chiral diarylbromobismuthines with arylmagnesium bromides.The NMR spectra of some of the new compounds exhibit diastereotopic effects, associated with the chirality, indicating that the bismuthines have a stable pyramidal configuration.
