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C31H28BF2I2N3O is a complex organic molecule composed of 31 carbon atoms, 28 hydrogen atoms, 2 boron atoms, 2 iodine atoms, 3 nitrogen atoms, and 1 oxygen atom. The presence of various functional groups, including boron and iodine, suggests unique chemical properties. The nitrogen and oxygen atoms indicate potential reactivity with other molecules or biological systems, while the large carbon and hydrogen content implies a hydrophobic nature. Further investigation and analysis are required to fully understand its potential applications and interactions.

1608488-47-6

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1608488-47-6 Usage

Uses

Used in Pharmaceutical Industry:
C31H28BF2I2N3O can be used as a pharmaceutical compound for its potential reactivity with biological systems. The presence of nitrogen and oxygen atoms may allow it to interact with enzymes, receptors, or other biomolecules, making it a candidate for drug development.
Used in Chemical Synthesis:
C31H28BF2I2N3O can be used as a starting material or intermediate in the synthesis of other complex organic compounds. Its unique structure and functional groups may enable the formation of new chemical entities with specific properties or applications.
Used in Material Science:
C31H28BF2I2N3O, due to its hydrophobic nature and the presence of boron and iodine atoms, may have potential applications in the development of new materials with specific properties, such as high thermal stability, electrical conductivity, or optical characteristics.
Used in Analytical Chemistry:
The unique composition of C31H28BF2I2N3O may make it a useful reagent or standard in analytical chemistry for the detection, quantification, or separation of other compounds.
Used in Environmental Applications:
C31H28BF2I2N3O may have potential uses in environmental remediation or monitoring, such as the detection of pollutants, the degradation of contaminants, or the development of new materials for water or air purification.
Note: The specific applications listed above are hypothetical and based on the general properties suggested by the molecular formula. Further research and experimentation would be necessary to confirm the suitability of C31H28BF2I2N3O for these uses.

Check Digit Verification of cas no

The CAS Registry Mumber 1608488-47-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,8,4,8 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1608488-47:
(9*1)+(8*6)+(7*0)+(6*8)+(5*4)+(4*8)+(3*8)+(2*4)+(1*7)=196
196 % 10 = 6
So 1608488-47-6 is a valid CAS Registry Number.

1608488-47-6Downstream Products

1608488-47-6Relevant academic research and scientific papers

Resonance energy transfer-enhanced rhodamine-styryl Bodipy dyad triplet photosensitizers

Ma, Jie,Yuan, Xiaolin,Kuecuekoez, Betuel,Li, Shengfu,Zhang, Caishun,Majumdar, Poulomi,Karatay, Ahmet,Li, Xiaohuan,Gul Yaglioglu,Elmali, Ayhan,Zhao, Jianzhang,Hayvali, Mustafa

, p. 3900 - 3913 (2014/05/20)

Organic triplet photosensitizers (R-1 and R-2) enhanced with the resonance energy transfer (RET) effect were prepared. Rhodamine was used as an intramolecular energy donor, and iodo-styryl-Bodipy was used as intramolecular energy acceptor/spin converter.

Switching of the triplet excited state of styryl 2,6-diiodo-bodipy and its application in acid-activatable singlet oxygen photosensitizing

Huang, Ling,Yang, Wenbo,Zhao, Jianzhang

, p. 10240 - 10255 (2015/02/19)

IodoBodipy-styrylBodipy dyads triplet photosensitizers were prepared (B-1 and B-2) which contain acid-responsive moiety. Both compounds show broadband visible light absorption, due to the resonance energy transfer (RET) between the two different visible l

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