1400813-90-2

Basic information

• Product Name: C₂₆H₂₅BF₂N₂O₂
• Synonyms: C₂₆H₂₅BF₂N₂O₂
• CAS NO: 1400813-90-2
• Molecular Weight: 446.305
• Mol File: 1400813-90-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: C₂₆H₂₅BF₂N₂O₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₆H₂₅BF₂N₂O₂(1400813-90-2)
• EPA Substance Registry System: C₂₆H₂₅BF₂N₂O₂(1400813-90-2)

Safety Data

• Hazardous Substances Data: 1400813-90-2(Hazardous Substances Data)

Upstream product

• 2386-26-7 ethyl 4-acetyl-3,5-dimethylpyrrole-2-carboxylate 
• 2400-36-4 6-methoxy-3-methyl-1H-indole 
• 2400-35-3 ethyl 6-methoxy-3-methyl-1H-indole-2-carboxylate 
• 123-54-6 acetylacetone 
• 2473-98-5 3-methyl-6-methoxyindole-2-carboxylic acid 
• 536-90-3 m-Anisidine 
• 2386-25-6 2,4-dimethyl-3-acetylpyrrole 
• 517-22-6 2,4-dimethyl-3-ethyl-pyrrole 
• 1353547-97-3 2-benzoyl-3-methyl-6-methoxyindole 
• 1353548-02-3 (MeO(H₃C)C₈H₃NC(C₆H₅)C₄N(CH₃)2(CH₂CH₃))BF₂ 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 1400813-93-5 C₃₃H₃₁BF₂N₄O₂ 
• 1400813-91-3 C₂₅H₂₃BF₂N₂O₂ 

Relevant articles and documents

Fused dual boron core based BODIPY dyes: synthesis and optical character

Here we report that two boron dipyrromethene derivatives (BNB-1 and BNB-2), bearing double boron atomic centers, have been synthesized and characterized. The additional boron atom was introduced into the skeleton of typical BODIPY dyes through the reactio

SPIROBODIPYs with spiropyran structure compound, preparation method and its use

The invention discloses a SPIROBODIPYs compound with the spiropyrane structure. The compound has the following structural general formula (refer to the Specification), wherein R1, R2, R3 and R4 are alkyl substituents or aromatic substituents, R5 is an alkyl substituent, an alcohol hydroxyl substituent or a substituent with triple bonds at the tail end. The invention further discloses the application of the SPIROBODIPYs compound to a fluorescence molecular probe. The SPIROBODIPYs compound can be applied to controllable detection of physiological and pathological process of cells, and can be used for building living cell acid organelles or used as a novel fluorescent dye of a fluorescence molecular probe for detecting the acid environment of cancer cells.

Target-triggered deprotonation of 6-hydroxyindole-based BODIPY: Specially switch on NIR fluorescence upon selectively binding to Zn2+

Based on 6-hydroxyindole BODIPY with a Schiff-base structure, NIR fluorescence with impressively high selectivity is triggered by deprotonation of the phenol group upon binding with Zn2+ due to the chelation-enhanced fluorescence effect, thus realizing a promising application in bioimaging of Zn2+. The Royal Society of Chemistry 2012.