2,2'-bis-(trifluoromethyl)-4,4'-dinitro-1,1'-biphenyl
2,2'-bis(trifluoromethyl)benzidine
Conditions | Yield |
---|---|
With ammonium formate; zinc In methanol at 50℃; Temperature; Concentration; | 96.83% |
With palladium 10% on activated carbon; hydrogen In ethanol at 80℃; under 15001.5 Torr; Catalytic behavior; Pressure; Temperature; | 92% |
With hydrogenchloride; tin | |
With hydrogen; palladium on activated charcoal In toluene at 60℃; under 7500.75 Torr; for 6h; Autoclave; |
Conditions | Yield |
---|---|
With sulfuric acid In water; toluene for 5h; Product distribution / selectivity; | 95.1% |
With hydrogenchloride In water; toluene at 25℃; for 3h; Product distribution / selectivity; | 95% |
With sulfuric acid In water at -5 - 75℃; under 2280.15 - 3800.26 Torr; for 2h; Temperature; Inert atmosphere; | 60% |
1,2-bis((3-trifluoromethyl)phenyl)diazene
A
2,2'-bis(trifluoromethyl)benzidine
B
4,2'-bis-trifluoromethyl-biphenyl-2,4'-diyldiamine
Conditions | Yield |
---|---|
With sodium amalgam; ethanol; sulfuric acid |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: lead; sodium acetate; aqueous ethanol 2: sodium-amalgam; aqueous ethanol; H2SO4 View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: H2SO4; HNO3 2: aq.-ethanolic NaOH 3: acetic acid; sulfuric acid; aqueous sodium nitrite solution; aqueous potassium iodide solution 4: copper-powder / 300 °C 5: tin; aq.-ethanolic HCl View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: acetic acid; sulfuric acid; aqueous sodium nitrite solution; aqueous potassium iodide solution 2: copper-powder / 300 °C 3: tin; aq.-ethanolic HCl View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: aq.-ethanolic NaOH 2: acetic acid; sulfuric acid; aqueous sodium nitrite solution; aqueous potassium iodide solution 3: copper-powder / 300 °C 4: tin; aq.-ethanolic HCl View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: copper-powder / 300 °C 2: tin; aq.-ethanolic HCl View Scheme |
Conditions | Yield |
---|---|
With sodium hydroxide; sulfuric acid; ammonium chloride; ammonia In methanol; acetone; toluene |
2,2'-bis(trifluoromethyl)benzidine
Conditions | Yield |
---|---|
With water; sodium hydroxide In dichloromethane for 4h; Solvent; Reflux; | 115 g |
2,2'-bis(trifluoromethyl)benzidine
Conditions | Yield |
---|---|
With water; sodium hydroxide In dichloromethane for 4h; Reflux; | 126.5 g |
2,2'-bis(trifluoromethyl)benzidine
Conditions | Yield |
---|---|
With water; sodium hydroxide In dichloromethane for 4h; Reflux; | 120.7 g |
2,2'-bis(trifluoromethyl)benzidine
Conditions | Yield |
---|---|
With water; sodium hydroxide In dichloromethane for 4h; Reflux; | 119.5 g |
2,2'-bis(trifluoromethyl)benzidine
Conditions | Yield |
---|---|
With water; sodium hydroxide In dichloromethane for 4h; Reflux; | 81.8 g |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: dichloromethane / 0 - 20 °C 2.1: sodium hydroxide / dichloromethane / 0.5 h / 20 °C 2.2: 5 h / 65 °C 3.1: water; sodium hydroxide / dichloromethane / 4 h / Reflux View Scheme |
1-(tert-butoxycarbonyl)-L-proline
2,2'-bis(trifluoromethyl)benzidine
Conditions | Yield |
---|---|
With N-(3-dimethylaminopropyl)-N-ethylcarbodiimide In dichloromethane at 20℃; for 2h; | 96% |
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 2h; | 96% |
Conditions | Yield |
---|---|
With pyridine In tetrahydrofuran Cooling with ice; | 95.7% |
With pyridine In N,N-dimethyl acetamide at 80℃; for 3h; | 65.4% |
Conditions | Yield |
---|---|
In ethanol at 20℃; for 3h; Reflux; | 94.15% |
2,2'-bis(trifluoromethyl)benzidine
Conditions | Yield |
---|---|
94% |
Conditions | Yield |
---|---|
In ethanol at 20℃; for 3h; Reflux; | 93.35% |
Conditions | Yield |
---|---|
With 4-hydroxymethyl-1,3-dioxolan-2-one at 180℃; for 14h; | 91.8% |
pyridine-2-carbaldehyde
Diethyl phosphonate
2,2'-bis(trifluoromethyl)benzidine
Conditions | Yield |
---|---|
With water at 45℃; for 0.5h; Sonication; Green chemistry; | 91.76% |
Diethyl phosphonate
2,2'-bis(trifluoromethyl)benzidine
4-fluorobenzaldehyde
Conditions | Yield |
---|---|
With water at 45℃; for 0.5h; Sonication; Green chemistry; | 91.42% |
Diethyl phosphonate
2,2'-bis(trifluoromethyl)benzidine
3-nitro-benzaldehyde
Conditions | Yield |
---|---|
With water at 45℃; for 0.5h; Reagent/catalyst; Temperature; Time; Sonication; Green chemistry; | 91.07% |
Diethyl phosphonate
2,2'-bis(trifluoromethyl)benzidine
4-chlorobenzaldehyde
Conditions | Yield |
---|---|
With water at 45℃; for 0.5h; Sonication; Green chemistry; | 90.46% |
Diethyl phosphonate
2,2'-bis(trifluoromethyl)benzidine
4-ethylbenzylaldehyde
Conditions | Yield |
---|---|
With water at 45℃; for 0.5h; Sonication; Green chemistry; | 90.35% |
Diethyl phosphonate
2,2'-bis(trifluoromethyl)benzidine
benzaldehyde
Conditions | Yield |
---|---|
With water at 45℃; for 0.5h; Sonication; Green chemistry; | 89.91% |
Diethyl phosphonate
2,2'-bis(trifluoromethyl)benzidine
4-dimethylamino-benzaldehyde
Conditions | Yield |
---|---|
With water at 45℃; for 0.5h; Sonication; Green chemistry; | 89.17% |
Diethyl phosphonate
2,2'-bis(trifluoromethyl)benzidine
4-hydroxy-benzaldehyde
Conditions | Yield |
---|---|
With water at 45℃; for 0.5h; Sonication; Green chemistry; | 88.23% |
thiophene-2-carbaldehyde
Diethyl phosphonate
2,2'-bis(trifluoromethyl)benzidine
Conditions | Yield |
---|---|
With water at 45℃; for 0.5h; Sonication; Green chemistry; | 87.79% |
Diethyl phosphonate
2,2'-bis(trifluoromethyl)benzidine
4-methoxy-benzaldehyde
Conditions | Yield |
---|---|
With water at 45℃; for 0.5h; Sonication; Green chemistry; | 86.68% |
2,2'-bis(trifluoromethyl)benzidine
Conditions | Yield |
---|---|
Stage #1: 2,2'-bis(trifluoromethyl)benzidine With sulfuric acid; sodium nitrite In water at 2 - 65℃; for 1h; Stage #2: With hydrogen bromide; copper(I) bromide at 45℃; Reagent/catalyst; | 86% |
With tert.-butylnitrite; copper(ll) bromide | 60% |
Conditions | Yield |
---|---|
With propionic acid at 150℃; for 10h; | 80% |
Conditions | Yield |
---|---|
Stage #1: 2,2'-bis(trifluoromethyl)benzidine; C19H8F6O7 In 1-methyl-pyrrolidin-2-one at 90℃; for 1h; Stage #2: With pyridine; acetic anhydride In 1-methyl-pyrrolidin-2-one at 90℃; for 2h; Temperature; | 80% |
2,2'-bis(trifluoromethyl)benzidine
2,2'-bis(trifluoromethyl)-4,4'-diiodobiphenyl
Conditions | Yield |
---|---|
Stage #1: 2,2'-bis(trifluoromethyl)benzidine With sulfuric acid; sodium nitrite In water; acetic acid at 5℃; for 1h; Stage #2: With potassium iodide In water for 3h; | 78.4% |
Stage #1: 2,2'-bis(trifluoromethyl)benzidine With hydrogenchloride; sodium nitrite In water at 0 - 5℃; Stage #2: With iodine; sodium iodide In dichloromethane; water at 5 - 20℃; | 75% |
With sodium iodide; sulfuric acid; iodine; sodium hydrogensulfite; sodium nitrite In dichloromethane; water | 13.3 grams (78%) |
Stage #1: 2,2'-bis(trifluoromethyl)benzidine With sulfuric acid; sodium nitrite Stage #2: With iodine; sodium iodide Further stages.; |
2,2'-bis(trifluoromethyl)benzidine
3-methyl-4-nitro-benzoyl chloride
Conditions | Yield |
---|---|
With pyridine In tetrahydrofuran at 20℃; for 12h; Sealed tube; Cooling with ice; | 76% |
2,2'-bis(trifluoromethyl)benzidine
Conditions | Yield |
---|---|
With uranyl nitrate hydrate; water; trifluoroacetic acid for 96h; Irradiation; Inert atmosphere; | 75% |
Stage #1: 2,2'-bis(trifluoromethyl)benzidine With hydrogenchloride; sodium nitrite In water at -4℃; for 2h; Inert atmosphere; Stage #2: With phosphoric acid In water at 20℃; for 25h; Inert atmosphere; Reflux; | 46.9% |
Stage #1: 2,2'-bis(trifluoromethyl)benzidine With methanesulfonic acid In water Stage #2: With sodium nitrite In water at 10 - 20℃; for 12h; Stage #3: With sulfuric acid; water at 120℃; |
2,2'-bis(trifluoromethyl)benzidine
Conditions | Yield |
---|---|
With bromine In methanol at 20℃; for 14h; Reflux; | 75% |
Conditions | Yield |
---|---|
Stage #1: 2,2'-bis(trifluoromethyl)benzidine; pyromellitic acid monoanhydride In 1-methyl-pyrrolidin-2-one; N,N-dimethyl acetamide at 90℃; for 1h; Stage #2: With pyridine; acetic anhydride In 1-methyl-pyrrolidin-2-one; N,N-dimethyl acetamide; toluene at 90℃; | 72% |
Stage #1: 2,2'-bis(trifluoromethyl)benzidine; pyromellitic acid monoanhydride In 1-methyl-pyrrolidin-2-one at 90℃; for 1h; Stage #2: With pyridine; acetic anhydride In 1-methyl-pyrrolidin-2-one at 90℃; for 2h; |
Conditions | Yield |
---|---|
With propionic acid at 150℃; for 10h; | 70% |
Conditions | Yield |
---|---|
With acetic acid Reflux; | 56.1% |
Conditions | Yield |
---|---|
With potassium nitrate at 5 - 10℃; for 72h; | 51% |
The Molecular Structure of 2,2'-Bis-(trifluormethyl) benzidine (CAS NO.341-58-2):
Molecular Formula: C14H10F6N2
Molecular Weight: 320.233019 g/mol
IUPAC: 4-[4-amino-2-(trifluoromethyl)phenyl]-3-(trifluoromethyl)aniline
Product Categories: Biphenyls (for High-Performance Polymer Research);Functional Materials;Reagent for High-Performance Polymer ResearchNominal Mass: 320 Da
Average Mass: 320.233 Da
Monoisotopic Mass: 320.074818 Da
Nominal Mass: 320 Da
Average Mass: 320.233 Da
Monoisotopic Mass: 320.074818 Da
Index of Refraction: 1.524
Molar Refractivity: 69.27 cm3
Molar Volume: 226.2 cm3
Surface Tension: 34 dyne/cm
Density: 1.415 g/cm3
Flash Point: 171.4 °C
Enthalpy of Vaporization: 62.46 kJ/mol
Boiling Point: 376.9 °C at 760 mmHg
Vapour Pressure: 7.02E-06 mmHg at 25°C
Hazard Codes: TXi
Risk Statements: 22-45-50/53
R22:Harmful if swallowed
R45:May cause cancer
R50/53:Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment
Safety Statements: 22-36/37/39-45
S22:Do not breathe dust
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection
S45:In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
RIDADR: 2811
Hazard Note: Toxic
HazardClass: IRRITANT-HARMFUL
2,2'-Bis-(trifluormethyl) benzidine (CAS NO.341-58-2) is also called as 4,4'-diamino-2,2'-bis(trifluoromethyl)biphenyl ; 22Tfmb ; 2,2'-Di(trifluoromethyl)benzidine ; 2,2'-Bis(trifluoromethyl)-4,4'-diamino biphenyl ; 2,2'-Bis(trifluoromethyl)benzidine 97% .
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