165320-27-4

Basic information

• Product Name: 9H-Fluoren-2-amine, N-(9,9-dimethyl-9H-fluoren-2-yl)-9,9-dimethyl-N-phenyl-
• CAS NO: 165320-27-4
• Molecular Formula: C36H31N
• Molecular Weight: 477.649
• Mol File: 165320-27-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 9H-Fluoren-2-amine, N-(9,9-dimethyl-9H-fluoren-2-yl)-9,9-dimethyl-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 9H-Fluoren-2-amine, N-(9,9-dimethyl-9H-fluoren-2-yl)-9,9-dimethyl-N-phenyl-(165320-27-4)
• EPA Substance Registry System: 9H-Fluoren-2-amine, N-(9,9-dimethyl-9H-fluoren-2-yl)-9,9-dimethyl-N-phenyl-(165320-27-4)

Safety Data

• Hazardous Substances Data: 165320-27-4(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 144981-85-1 2-iodo-9,9-dimethyl-9H-fluorene 
• 28320-31-2 2-bromo-9,9-dimethyl-9H-fluorene 

Downstream Products

• 1284240-04-5 1-(4-(bis(9,9-dimethyl-9H-fluoren-2-yl)amino)phenyl)ethanone 
• 1383782-66-8 2-[N,N-bis-(9,9-dimethylfluoren-2-yl)aminophenyl]-2'-bromo-5,5'-bisthiophene 
• 1389321-71-4 2-[N,N-bis-(9,9-dimethylfluoren-2-yl)aminophenyl]-5,5'-bithiophene-2' boronic acid pinacol ester 
• 1389321-72-5 4-[2-(N,N-bis-(9,9-dimethylfluoren-2-yl)-4-aminophenyl)-5,5'-bisthiophene-2']phthalonitrile 
• 916246-05-4 4-[N,N-bis(9,9-dimethylfluoren-2-yl)amino]-benzaldehyde 
• 948560-42-7 C₃₆H₃₀IN 
• 313050-72-5 2-[N,N-bis(9,9-dimethylfluoren-2-yl)-4-aminophenyl]-thiophene 
• 313050-71-4 N-(4-bromophenyl)-N-(9,9-dimethyl-9H-fluoren-2-yl)-9,9-dimethyl-9H-fluoren-2-amine 

Relevant articles and documents

Synthesis and dye sensitized solar cell applications of Bodipy derivatives with bis-dimethylfluorenyl amine donor groups

Three Bodipy dyes with strong absorptivities in the visible and near infrared regions were designed, synthesized and their potential as photosensitizers for liquid electrolyte-based dye sensitized solar cells have been evaluated. For the first time Bodipy derivatives with bis-dimethylfluorenyl amine donor groups which were known for their bulky structures as donor groups have been used together. We altered our mostly used triphenylamine group with these and investigated the dye-sensitized solar cell efficiencies of this new class of Bodipy dyes.

Convergent synthesis of near-infrared absorbing, "push-pull", bisthiophene-substituted, zinc(II) phthalocyanines and their application in dye-sensitized solar cells

Zinc(II) phthalocyanine dyes that contain triarylamine-terminated bisthiophene and hexylbisthiophene groups have been synthesized by a convergent approach by using carboxytriiodo-ZnPc as a precursor. Further transformation of the iodo groups by a Pd-catal

DYE-SENSITIZED PHOTOELECTRIC CONVERSION DEVICE

Disclosed is a photoelectric conversion device wherein a methine dye represented by the formula (1) below is supported by a thin film of oxide semiconductor particles arranged on a substrate. Also disclosed is a solar cell manufactured by using such a photoelectric conversion device. (In the formula (1), n represents an integer of 0-5; m represents an integer of 0-5; R1-R4 independently represent a hydrogen atom, an optionally substituted aromatic residue, an optionally substituted aliphatic hydrocarbon residue or the like; X and Y independently represent a hydrogen atom; an optionally substituted aromatic residue, an optionally substituted aliphatic hydrocarbon residue or the like; Z represents an oxygen atom, a sulfur atom or the like; A1, A2, A3, A4 and A5 independently represent a hydrogen atom, an optionally substituted aromatic residue, an optionally substituted aliphatic hydrocarbon residue or the like; and rings a, b and c may be substituted.)