4,4'-(9-Fluorenylidene)dianiline

HCID 631552

Basic information

CAS
15499-84-0
Standard SMILES
Nc1ccc(C2(c3ccc(N)cc3)c3ccccc3-c3ccccc32)cc1
InChIKey
KIFDSGGWDIVQGN-UHFFFAOYSA-N
Molecular formula
C25H20N2
Average molar mass
348.4 g/mol
Monoisotopic mass
348.16264864

Names & identifiers

Preferred name
4,4'-(9-Fluorenylidene)dianiline
IUPAC
4-[9-(4-aminophenyl)fluoren-9-yl]aniline
English name
9,9-Bis(4-aminophenyl)fluorene
Molecular formula
C25H20N2
Molecular weight
348.44

Names & synonyms

4,4'-(9-Fluorenylidene)dianilineRefChem:506470628-740-515499-84-04,4'-(9H-fluorene-9,9-diyl)dianiline9,9-Bis(4-aminophenyl)fluorene4-[9-(4-aminophenyl)fluoren-9-yl]anilineBenzenamine, 4,4'-(9H-fluoren-9-ylidene)bis-MFCD000391564-[9-(4-aminophenyl)-9H-fluoren-9-yl]anilineC25H20N24,4/'-(9-Fluorenylidene)dianiline
Show more names
FDABAFLBAF/FDAFDA/BAFLAKOS BBB/416Zinc03897005AnilinefluoreneBIO-FARMA BF003152TIMTEC-BB SBB008629
9,9-Bis(4-aminophenyl)fluorene (FDA)4,4 inverted exclamation marka-(9-Fluorenylidene)dianiline4-[9-(4-aminophenyl)fluoren-9-yl]phenylamineSMR000203330MLS000584167SCHEMBL105428CHEMBL341910SCHEMBL1259227

Database identifiers

CAS
15499-84-0
PubChem CID
631552
DTXSID
DTXSID20348173
ChEMBL
CHEMBL341910
EC Number
628-740-5
Nikkaji
J111.263E

Properties

Computed structural properties

XLogP
5.3
Topological polar surface area
52 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
2
Rotatable bonds
2
Heavy atoms
27

Physicochemical properties

Melting point
237 · 237-239 °C (lit.)
Boiling point
535.2 · 535.2±50.0 °C(Predicted)
Density
1.245 · 1.245±0.06 g/cm3(Predicted)
storage temp.
Keep in dark place,Inert atmosphere,Room temperature
Water Solubility
Insoluble in water
form
powder to crystal

Safety & regulation

GHS classification

GHS Classification · 4 items

Warning

H302 (95.1%): Harmful if swallowed [Warning Acute toxicity, oral]

P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P330, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 41 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Hazard information

Regulatory InformationPMN - indicates a commenced PMN (Pre-Manufacture Notices) substance.
Hazard Classes and CategoriesAcute Tox. 4 (95.1%)

Safety data

PPE
dust mask type N95 (US), Eyeshields, Gloves
wgk
3
tsca
TSCA listed
hs_code
29215900
risk_code
20/21/22-36/37
Signal word
Warning

Chemistry & industry

Uses & manufacturing

General Manufacturing InformationBenzenamine, 4,4'-(9H-fluoren-9-ylidene)bis-: ACTIVE
Applications · 3 items

Description9,9-Bis(4-aminophenyl)fluorene (FDA) is a fluorene derivative with two aminophenyl substituents on the 9-position. This compound has partial conjugation and can be utilized as a dopant-free organic hole-transporting material in inverted perovskite solar cells. Due to its diaminophenyl groups, FDA is commonly employed in synthesizing polyimides that possess high thermal and hydrolytic stability for optical fiber light guide coatings. Because the FDA is not fully aromatized, it is chosen to produce thermally stable transparent polyimides. Additionally, the polyimide derived from 9,9-bis(4-aminophenyl)fluorene can be further modified through Friedel-Crafts alkylation on the fluorene moiety, as the polyimide backbone remains chemically stable.

Uses9,9-bis(4-aminophenyl)fluorene be used for preparation of high-strength material and high-temperature polymers.

General Description4,4′-(9-Fluorenylidene)dianiline is a diamine.

Preparation methods · 1 item

PreparationThe synthesis of 9,9-Bis(4-aminophenyl)fluorene can be carried out through the following stepwise procedure:Prepare the reaction mixture:Place 3.6 g of fluorenone (20 mmol), 7.2 g of aniline hydrochloride (55.6 mmol), 0.5 g of sodium bisulfite (4.8 mmol), 8.8 mL of aniline (96.4 mmol), and 6 mL of toluene in a 100 mL two-necked flask.Ensure the reaction is conducted under nitrogen protection.Add a water separator to the two-necked flask.Begin the reaction:Stir the reaction mixture and slowly increase the temperature to 120 °C.Allow the reaction to continue for 30 minutes.Separate the green liquid produced in the water separator.Further reaction at elevated temperature:Continue the reaction at 120 °C for an additional 3 hours.Separate the water produced in the water separator.Increase temperature and maintain reaction:Slowly raise the temperature to 135 °C.Keep the reaction at this temperature for 1.5 hours.Monitor for completion:Check the water separator for any further production of water.Cease the reaction when no more water is produced in the water separator.Cool down and adjust pH:Allow the reacted material to cool to around 60 ℃.Add 10 wt% potassium hydroxide solution to the reaction mixture.Adjust the pH of the mixture to 9.Stir the solution for 15 minutes while it is still hot.Filtration and purification:Filter the solution to remove any solid impurities.Wash the filter cake with water.Recrystallize the washed filter cake using 30 mL of toluene.Filter the recrystallized product to obtain pure rice-white product.Yield determination:Weigh the obtained pure product, which should amount to 6.55 g.Calculate the yield by dividing the obtained mass by the theoretical maximum mass and multiplying by 100%.The yield of the pure rice-white product should be 94%.

Upstream & downstream products

Suppliers100 total

梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
衢州润东化工有限公司0570-8789886 18892685668 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
合肥翰刚医药科技有限公司+8618062405514 · [email protected]
中节能万润股份有限公司0535-6101880 · [email protected]

Related reactions

7 records

Compound notes

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