fluorobenzene
benzene-1,3-dicarbonyl dichloride
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With aluminium trichloride at 23℃; for 4h; Friedel-Crafts acylation; | 98% |
Stage #1: benzene-1,3-dicarbonyl dichloride With aluminum (III) chloride In dichloromethane for 0.5h; Friedel-Crafts Acylation; Inert atmosphere; Reflux; Stage #2: fluorobenzene In dichloromethane for 12h; Friedel-Crafts Acylation; Inert atmosphere; | 56% |
Stage #1: benzene-1,3-dicarbonyl dichloride With aluminum (III) chloride In dichloromethane for 0.5h; Reflux; Stage #2: fluorobenzene In dichloromethane for 12h; Reflux; | 42% |
With aluminum (III) chloride for 8h; Friedel-Crafts Acylation; Inert atmosphere; | 3.24 g |
tris(4-fluorophenyl)bismuthane
benzene-1,3-dicarbonyl dichloride
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With triethylamine; tetrakis(triphenylphosphine) palladium(0) In 1,4-dioxane at 80℃; for 3h; | 76% |
With tributyl-amine In 1-methyl-pyrrolidin-2-one at 80℃; for 4h; Schlenk technique; Inert atmosphere; | 74% |
4,4'-Dihydroxybiphenyl
2,3-dihydroxynaphthalene-6-sulphonic acid sodium salt
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With potassium carbonate In 1-methyl-pyrrolidin-2-one at 160 - 170℃; | 100% |
4,4'-Dihydroxybiphenyl
2,3-dihydroxynaphthalene-6-sulphonic acid sodium salt
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With potassium carbonate In 1-methyl-pyrrolidin-2-one at 160 - 170℃; | 100% |
4,4'-Dihydroxybiphenyl
2,3-dihydroxynaphthalene-6-sulphonic acid sodium salt
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With potassium carbonate In 1-methyl-pyrrolidin-2-one at 160 - 170℃; | 100% |
4,4'-Dihydroxybiphenyl
2,3-dihydroxynaphthalene-6-sulphonic acid sodium salt
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With potassium carbonate In 1-methyl-pyrrolidin-2-one at 160 - 170℃; | 100% |
4,4'-Dihydroxybiphenyl
2,3-dihydroxynaphthalene-6-sulphonic acid sodium salt
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With potassium carbonate In 1-methyl-pyrrolidin-2-one at 160 - 170℃; | 100% |
2,3-dihydroxynaphthalene-6-sulphonic acid sodium salt
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With potassium carbonate In 1-methyl-pyrrolidin-2-one at 160 - 170℃; | 100% |
2,3-dihydroxynaphthalene-6-sulphonic acid sodium salt
hydroquinone
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With potassium carbonate In 1-methyl-pyrrolidin-2-one at 160 - 170℃; | 100% |
2,3-dihydroxynaphthalene-6-sulphonic acid sodium salt
hydroquinone
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With potassium carbonate In 1-methyl-pyrrolidin-2-one at 160 - 170℃; | 100% |
2,3-dihydroxynaphthalene-6-sulphonic acid sodium salt
hydroquinone
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With potassium carbonate In 1-methyl-pyrrolidin-2-one at 160 - 170℃; | 100% |
2,3-dihydroxynaphthalene-6-sulphonic acid sodium salt
hydroquinone
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With potassium carbonate In 1-methyl-pyrrolidin-2-one at 160 - 170℃; | 100% |
2,3-dihydroxynaphthalene-6-sulphonic acid sodium salt
hydroquinone
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With potassium carbonate In 1-methyl-pyrrolidin-2-one at 160 - 170℃; | 100% |
Conditions | Yield |
---|---|
With potassium carbonate In 1-methyl-pyrrolidin-2-one at 160℃; for 4h; Schlenk technique; Inert atmosphere; | 95% |
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid In (2S)-N-methyl-1-phenylpropan-2-amine hydrate | 87.3% |
Conditions | Yield |
---|---|
With potassium carbonate In hexane; N,N-dimethyl acetamide for 18h; Heating; | 75% |
m-Hydroxyaniline
1,3-bis(4'-fluorobenzoyl)benzene
1,3-bis[4-(3-aminophenoxy)benzoyl]benzene
Conditions | Yield |
---|---|
Stage #1: m-Hydroxyaniline With potassium carbonate In N,N-dimethyl-formamide; toluene Dean-Stark trap; Reflux; Stage #2: 1,3-bis(4'-fluorobenzoyl)benzene In N,N-dimethyl-formamide; toluene at 130 - 150℃; Inert atmosphere; | 64.4% |
sodium acetylide
1,3-bis(4'-fluorobenzoyl)benzene
1,3-di[1-hydroxy-1-(p-fluorophenyl)-prop-2-ynyl]benzene
Conditions | Yield |
---|---|
With acetylene In tetrahydrofuran; dimethyl sulfoxide at 23℃; | 64% |
(S)-[1,1']-binaphthalenyl-2,2'-diol
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 150℃; for 9h; | 64% |
thiosemicarbazide
1,3-bis(4'-fluorobenzoyl)benzene
1,3-bis-(4-fluorobenzoyl)benzene thiosemicarbazone
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In methanol for 10h; Reflux; | 52% |
With toluene-4-sulfonic acid In methanol for 10h; Inert atmosphere; Reflux; | 52% |
4,4'-Dihydroxybiphenyl
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl acetamide; toluene for 8h; Cyclo-condensation; Heating; | A 7.7% B 15% |
9H-carbazole
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
With potassium tert-butylate In N,N-dimethyl-formamide at 120℃; for 24h; Inert atmosphere; | 12% |
1,3-bis(4'-fluorobenzoyl)benzene
C40H26N4O5
polymer, Mn 16824 by GPC, Mw 36525, ηinh 0.68 dL/g in CHCl3 at 25 deg C; monomer(s): 1,3-bis(4-fluorobenzoyl)benzene; O,O-bis(4-(1,2-dihydro-phthalazin-1-on-4-yl)phenyl)-4,4-dihydroxydiphenyl ether
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl acetamide; toluene at 145 - 180℃; for 22h; |
1,3-bis(4'-fluorobenzoyl)benzene
polymer, Mn 63403 by GPC, Mw 151167, ηinh 1.01 dL/g in CHCl3 at 25 deg C; monomer(s): 1,3-bis(4-fluorobenzoyl)benzene; O,O-bis(4-(1,2-dihydro-phthalazin-1-on-4-yl)phenyl)-4,4-oxybis(benzenethiol)
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl acetamide; toluene at 145 - 180℃; for 22h; |
1,3-bis(4'-fluorobenzoyl)benzene
C43H32N4O4
polymer, Mn 37852 by GPC, Mw 93547, ηinh 0.91 dL/g in CHCl3 at 25 deg C; monomer(s): 1,3-bis(4-fluorobenzoyl)benzene; O,O-bis(4-(1,2-dihydro-phthalazin-1-on-4-yl)phenyl)-4,4-isopropylidenebiphenol
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl acetamide; toluene at 145 - 180℃; for 22h; |
1,3-bis(4'-fluorobenzoyl)benzene
C43H26F6N4O4
polymer, Mn 31112 by GPC, Mw 55299, ηinh 0.41 dL/g in CHCl3 at 25 deg C; monomer(s): 1,3-bis(4-fluorobenzoyl)benzene; O,O-bis(4-(1,2-dihydro-phthalazin-1-on-4-yl)phenyl)-4,4-(hexafluoroisopropylidene)biphenol
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl acetamide; toluene at 145 - 180℃; for 22h; |
1,3-bis(4'-fluorobenzoyl)benzene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 64 percent / potassium carbonate / dimethylformamide / 9 h / 150 °C 2: 2 percent / potassium carbonate / toluene; dimethylformamide / 108 h / 150 °C View Scheme |
1,3-bis(4'-fluorobenzoyl)benzene
1,3-di-(3-p-fluorophenyl-[3H]-naphtho[2,1-b]pyran-3-yl)-benzene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 64 percent / acetylene / tetrahydrofuran; dimethylsulfoxide / 23 °C 2: 73 percent / PPTS; trimethyl orthoformate / CH2Cl2 / 6 h / Heating View Scheme |
1,3-bis(4'-fluorobenzoyl)benzene
1,3-di-(8-bromo-3-p-fluorophenyl-[3H]-naphtho[2,1-b]pyran-3-yl)-benzene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 64 percent / acetylene / tetrahydrofuran; dimethylsulfoxide / 23 °C 2: 86 percent / PPTS; trimethyl orthoformate / CH2Cl2 / 8 h / Heating View Scheme |
1,3-bis(4'-fluorobenzoyl)benzene
1,3-di-(2-p-fluorophenyl-6-phenyl-5-ethoxycarbonyl-[2H]-naphtho[2,1-b]pyran-2-yl)-benzene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 64 percent / acetylene / tetrahydrofuran; dimethylsulfoxide / 23 °C 2: 72 percent / PPTS; trimethyl orthoformate / CH2Cl2 / 6 h / Heating View Scheme |
The systematic name of 1,3-Bis(4-fluorobenzoyl)benzene is benzene-1,3-diylbis[(4-fluorophenyl)methanone] . With the CAS registry number 108464-88-6, it is also named as 1,3-Phenylenebis[(4-fluorophenyl)methanone] ; methanone, 1,1'-(1,3-phenylene)bis[1-(4-fluorophenyl)- . The product's categories are C15 to C38, carbonyl compounds and ketones. It is used as pharmaceutical intermediates. 1,3-Bis(4-fluorobenzoyl)benzene must be sealed in the container. Keep the container tightly sealed and store in a cool and dry place.
The other characteristics of this product can be summarized as: (1)ACD/LogP: 4.86 ; (2)# of Rule of 5 Violations: 0 ; (3)#H bond acceptors: 2 ; (4)#H bond donors: 0 ; (5)#Freely Rotating Bonds: 4 ; (6)Index of Refraction: 1.59 ; (7)Molar Refractivity: 85.82 cm3 ; (8)Molar Volume: 254 cm3 ; (9)Polarizability: 34.02×10-24 cm3 ; (10)Surface Tension: 45.7 dyne/cm ; (11)Enthalpy of Vaporization: 74 kJ/mol ; (12)Vapour Pressure: 3.08E-09 mmHg at 25°C.
People can use the following data to convert to the molecule structure. SMILES: O=C(c1ccc(F)cc1)c3cccc(C(=O)c2ccc(F)cc2)c3; InChI: InChI=1/C20H12F2O2/c21-17-8-4-13(5-9-17)19(23)15-2-1-3-16(12-15)20(24)14-6-10-18(22)11-7-14/h1-12H; InChIKey: PISLKPDKKIDMQT-UHFFFAOYAJ. The price of this product changes with the market.
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