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1256494-55-9

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1256494-55-9 Usage

Uses

Used in Pharmaceutical Development:
Used in Chemical Research:
In the field of chemical research, (5,5-difluoro-1,3,7,9-tetramethyl-5H-4λ4,5λ4-dipyrrolo[1,2-c:2′,1′-f ][1,3,2]diazaborinin-10-yl)methanol can be used as a starting material or a building block for the synthesis of more complex molecules. Its unique properties and reactivity may facilitate the development of novel chemical compounds with specific applications in various industries.
Used in Material Science:
(5,5-difluoro-1,3,7,9-tetramethyl-5H-4λ4,5λ4-dipyrrolo[1,2-c:2′,1′-f ][1,3,2]diazaborinin-10-yl)methanol may also find applications in material science, where its unique chemical structure could be utilized to create new materials with specific properties. These materials could have potential uses in various industries, such as electronics, aerospace, or automotive.
Used in Environmental Applications:
(5,5-difluoro-1,3,7,9-tetramethyl-5H-4λ4,5λ4-dipyrrolo[1,2-c:2′,1′-f ][1,3,2]diazaborinin-10-yl)methanol's potential interactions with biological systems may also make it useful in environmental applications, such as the development of biodegradable materials or the creation of compounds that can help in the remediation of environmental pollutants.

Check Digit Verification of cas no

The CAS Registry Mumber 1256494-55-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,4,9 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1256494-55:
(9*1)+(8*2)+(7*5)+(6*6)+(5*4)+(4*9)+(3*4)+(2*5)+(1*5)=179
179 % 10 = 9
So 1256494-55-9 is a valid CAS Registry Number.

1256494-55-9Upstream product

1256494-55-9Downstream Products

1256494-55-9Relevant articles and documents

Upconversion-like Photolysis of BODIPY-Based Prodrugs via a One-Photon Process

Lv, Wen,Li, Yafei,Li, Feiyang,Lan, Xin,Zhang, Yaming,Du, Lili,Zhao, Qiang,Phillips, David L.,Wang, Weiping

supporting information, p. 17482 - 17486 (2019/11/11)

Photochemical reactions at lower energy than the absorption window are currently achieved by multi-photon processes, including two-photon absorption and photon upconversion, which have limited energy utilization efficiency. Here, we report a one-photon strategy based on triplet-triplet energy transfer (TTET) between a photosensitizer and a photocleavable molecule to achieve photolysis at low energy. To verify this concept, we chose platinum(II) tetraphenyltetrabenzoporphyrin (PtTPBP) as the photosensitizer and synthesized a boron-dipyrromethene (BODIPY)-based prodrug as the photocleavable molecule. Photolysis of the prodrug is achieved by TTET upon excitation of PtTPBP at 625 nm with a photolysis quantum yield of 2.8%. Another demonstration shows an unexpected higher photolysis quantum yield than the direct excitation at 530 nm. This strategy opens a new path for achieving photolysis at long wavelengths, benefiting the applications in biological studies, photopharmacology, and photoresponsive drug delivery.

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