1256494-55-9

Basic information

• Product Name: (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
• Synonyms: (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
• CAS NO: 1256494-55-9
• Molecular Weight: 278.11
• Mol File: 1256494-55-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (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(CAS DataBase Reference)
• NIST Chemistry Reference: (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(1256494-55-9)
• EPA Substance Registry System: (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(1256494-55-9)

Safety Data

• Hazardous Substances Data: 1256494-55-9(Hazardous Substances Data)

Usage

General Description

The chemical "(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" is a complex organic compound with a molecular formula that includes fluorine, carbon, hydrogen, nitrogen, and boron. It is a derivative of diazaborinine, a class of boron-containing heterocyclic compounds. The addition of a methanol group to the diazaborinine molecule adds hydroxyl functionality, making it potentially useful in chemical and biological applications. The chemical structure of this compound provides a platform for potential interactions with various biological systems, making it potentially valuable in pharmaceutical development and research.

Upstream product

• 67-56-1 methanol 

Relevant articles and documents

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

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.