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ChemicalBook--->CAS DataBase List--->194235-40-0

194235-40-0

194235-40-0 Structure

194235-40-0 Structure
IdentificationBack Directory
[Name]

Difluoro{2-[(3,5-dimethyl-2H-pyrrol-2-ylidene-N)phenylmethyl]-3,5-dimethyl-1H-pyrrolato-N}boron
[CAS]

194235-40-0
[Synonyms]

BODIPY dye
Boron dipyrromethene fluorophore
1,3,5,7-tetramethy-8-phenyl-4,4-difluoroboradiazaindacene
1,3,5,7-Tetramethyl-8-phenyl-4,4-difluoroboradiazaindacene
1,3,5,7-Tetramethyl-8-phenyl-4,4-difluoroboradiazaindacene 97%
Difluoro{2-[(3,5-dimethyl-2H-pyrrol-2-ylidene-N)phenylmethyl]-3,5-dimethyl-1H-pyrrolato-N}boron
[2-[(3,5-dimethyl-2H-pyrrol-2-ylidene-κN)phenylmethyl]-3,5-dimethyl-1H-pyrrolato-κN]difluoro-Boron
5,5-difluoro-1,3,7,9-tetramethyl-10-phenyl-5H-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium-5-uide
[Molecular Formula]

C19H21BF2N2
[MDL Number]

MFCD28137455
[MOL File]

194235-40-0.mol
[Molecular Weight]

326.191
Chemical PropertiesBack Directory
[Melting point ]

174-179°C
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

Solid
[color ]

Orange to red
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

BODIPY laser dyes are used to generate fluorescent conjugates of proteins, nucleotides, oligonucleotides, and dextrans, and to prepare fluorescent enzyme substrates, fatty acids, phospholipids, lipopolysaccharides, receptor ligands, and polystyrene microspheres.
[Definition]

ChEBI: 4,4-difluoro-1,3,5,7-tetramethyl-8-phenyl-4-bora-3a,4a-diaza-s-indacene is a BODIPY dye.
[General Description]

1,3,5,7-Tetramethyl-8-phenyl-4,4-difluoroboradiazaindacene (BODIPY) is a difluoroboradiaza-s-indacene derivative that has high absorption coefficient and quantum yield with photonic properties. It is used as an acceptor molecule that facilitates the formation of fluorescent probes.
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