Conditions | Yield |
---|---|
With zinc(II) chloride at 255 - 258℃; for 21h; | 45% |
1-(dodec-1-yn-1-yl)-4-nitrobenzene
4-dodecylaniline
Conditions | Yield |
---|---|
With 5%-palladium/activated carbon; hydrogen In ethanol; ethyl acetate at 20℃; under 15001.5 Torr; for 24h; Autoclave; | 41% |
Conditions | Yield |
---|---|
With zinc(II) chloride at 240℃; |
Conditions | Yield |
---|---|
With cobalt(II) chloride at 247℃; |
1-chloro-4-dodecylbenzene
4-dodecylaniline
Conditions | Yield |
---|---|
With ammonia; water; copper(l) chloride |
4'-aminododecanoylphenone
4-dodecylaniline
Conditions | Yield |
---|---|
With hydrogenchloride; amalgamated zinc | |
With potassium hydroxide; hydrazine hydrate; diethylene glycol |
p'-(ω-(trimethylammonio)butyloxy)-p-(dodecylbenzylidene)aniline
A
4-dodecylaniline
B
4-(p-formylphenyloxy)butyltrimethylammonium bromide
Conditions | Yield |
---|---|
With phosphate buffer In water at 30℃; Rate constant; Kinetics; ΔE(excit.); influence of pH and concentration of azometine on velocity constant; |
[10-(4-{[(E)-4-Dodecyl-phenylimino]-methyl}-phenoxy)-decyl]-trimethyl-ammonium; bromide
A
4-dodecylaniline
B
10-(p-formylphenyloxy)decyltrimethylammonium bromide
Conditions | Yield |
---|---|
With phosphate buffer In water at 30℃; Rate constant; Kinetics; ΔE(excit.); influence of pH and concentration of azometine on velocity constant, var. solvents; |
(4-{[(E)-4-Dodecyl-phenylimino]-methyl}-phenyl)-trimethyl-ammonium; bromide
A
4-dodecylaniline
B
4-formyl-N,N,N-trimethyl-benzenaminium bromide
Conditions | Yield |
---|---|
With phosphate buffer In water at 30℃; Rate constant; Kinetics; ΔE(excit.); influence of pH and concetration of azometine on velocity constant; |
N-dodecylaniline
A
4-dodecylaniline
B
4,N-didodecyl-aniline
C
aniline
Conditions | Yield |
---|---|
at 250℃; |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: AlCl3 2: CuCl; aqueous NH3 / 250 - 270 °C 3: amalgamated zinc; aqueous HCl View Scheme | |
Multi-step reaction with 3 steps 1: AlCl3; CS2 2: ethanolic NaOH 3: N2H4+H2O; KOH; diethylene glycol View Scheme | |
Multi-step reaction with 3 steps 1: aluminum (III) chloride 2: hydrazine 3: aluminum (III) chloride; acetyl chloride View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: cobalt (II)-chloride / 247 °C View Scheme |
1-(4-chloro-phenyl)-dodecan-1-one
4-dodecylaniline
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: CuCl; aqueous NH3 / 250 - 270 °C 2: amalgamated zinc; aqueous HCl View Scheme | |
Multi-step reaction with 4 steps 1: aluminium isopropylate; isopropyl alcohol 2: KHSO4 / 200 °C / 10 Torr 3: Raney nickel; ethanol / Hydrogenation 4: water; CuCl; NH3 View Scheme |
acetic acid-(4-lauroyl-anilide)
4-dodecylaniline
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: ethanolic NaOH 2: N2H4+H2O; KOH; diethylene glycol View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: cobalt (II)-chloride / 247 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: AlCl3 2: CuCl; aqueous NH3 / 250 - 270 °C 3: amalgamated zinc; aqueous HCl View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: AlCl3; CS2 2: ethanolic NaOH 3: N2H4+H2O; KOH; diethylene glycol View Scheme |
1ξ-(4-chloro-phenyl)-dodec-1-ene
4-dodecylaniline
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: Raney nickel; ethanol / Hydrogenation 2: water; CuCl; NH3 View Scheme |
1-(4-chloro-phenyl)-dodecan-1-ol
4-dodecylaniline
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: KHSO4 / 200 °C / 10 Torr 2: Raney nickel; ethanol / Hydrogenation 3: water; CuCl; NH3 View Scheme |
Conditions | Yield |
---|---|
With aluminum (III) chloride; methyl tributylammonium chloride at 46 - 160℃; for 27.8h; |
Conditions | Yield |
---|---|
Stage #1: 1-dodecylbenzene With aluminum (III) chloride; acetyl chloride Stage #2: Schmidt reaction; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: hydrazine 2: aluminum (III) chloride; acetyl chloride View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: aluminum (III) chloride 2: hydrazine 3: aluminum (III) chloride; acetyl chloride View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); triethylamine / 2 h / 80 °C / Inert atmosphere 2: 5%-palladium/activated carbon; hydrogen / ethanol; ethyl acetate / 24 h / 20 °C / 15001.5 Torr / Autoclave View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); triethylamine / 2 h / 80 °C / Inert atmosphere 2: 5%-palladium/activated carbon; hydrogen / ethanol; ethyl acetate / 24 h / 20 °C / 15001.5 Torr / Autoclave View Scheme |
2-dodecylaniline
4-dodecylaniline
Conditions | Yield |
---|---|
With hydrogen sulfide |
4-dodecylaniline
5,11,17,23-tetraformyl-25,26,27,28-tetrakis(methoxy)calix[4]arene
C108H148N4O4
Conditions | Yield |
---|---|
With 4 A molecular sieve In chloroform for 29h; Heating; | 100% |
4-dodecylaniline
Conditions | Yield |
---|---|
In not given ligand reacted with Co salt instaneously; | 99% |
Conditions | Yield |
---|---|
Stage #1: cycl-isopropylidene malonate; trimethyl orthoformate for 1h; Reflux; Stage #2: 4-dodecylaniline for 2h; Reflux; | 98% |
Conditions | Yield |
---|---|
Stage #1: 4-dodecylaniline With 1H-imidazole; triethylamine In tetrahydrofuran for 0.166667h; Stage #2: acryloyl chloride In tetrahydrofuran at 0 - 25℃; for 15.33h; Inert atmosphere; | 95% |
With triethylamine In tetrahydrofuran at 0 - 20℃; for 15.16h; Inert atmosphere; | 95% |
4-dodecylaniline
Conditions | Yield |
---|---|
With iodine; sodium hydrogencarbonate In water; toluene at 20℃; Inert atmosphere; Schlenk technique; | 94% |
Conditions | Yield |
---|---|
In ethanol at 20℃; for 18h; | 91.5% |
Conditions | Yield |
---|---|
With acid | 90% |
4-dodecylaniline
ortho-chlorobenzoic acid
2-((4-dodecylphenyl)amino)benzoic acid
Conditions | Yield |
---|---|
With copper diacetate; potassium carbonate In N,N-dimethyl-formamide for 3h; Inert atmosphere; Reflux; | 90% |
Conditions | Yield |
---|---|
In acetonitrile at 80℃; under 760.051 Torr; for 0.25h; | 90% |
Conditions | Yield |
---|---|
Stage #1: 4-dodecylaniline With potassium carbonate In dichloromethane at 20℃; for 0.5h; Stage #2: chloroacetyl chloride In dichloromethane for 4h; Reflux; | 89% |
Stage #1: chloroacetyl chloride With potassium carbonate In dichloromethane at 20℃; for 0.5h; Stage #2: 4-dodecylaniline In dichloromethane for 4h; Reflux; | 89% |
3,5-dihydroxyphenol
4-dodecylaniline
1,3,5-tris(4-n-dodecylanilino)benzene
Conditions | Yield |
---|---|
iodine In toluene at 130℃; for 2h; | 87.8% |
4-dodecylaniline
2-hydroxy-4-n-dodecyloxybenzaldehyde
Conditions | Yield |
---|---|
With acetic acid In ethanol for 18h; Reflux; | 86% |
trans-(2,6-diformyl-3,5-bis(2,5,8,11-tetraoxadecyl)phenyl)chlorobis(triphenylphosphine)palladium
4-dodecylaniline
(3,5-bis(2,5,8,11-tetraoxadecyl)-2,6-bis(N-4-dodecylphenylimino)phenyl)chloropalladium
Conditions | Yield |
---|---|
With (H2N)2CO*H2O2 In acetonitrile (N2); refluxing soln. of palladium compd. and aniline deriv. in anhyd. CH3CN for 72 h, cooling to 25°C, addn. of urea hydrogen peroxide, stirring at 50°C for 11 h; evapn., chromy. (silica gel, 0-5% methanol/ethyl acetate), gel permeating chromy. (CHCl3), elem. anal.; | 85% |
Conditions | Yield |
---|---|
Stage #1: 4-dodecylaniline; phenylpropyolic acid With dmap In tetrahydrofuran at 0℃; for 0.166667h; Inert atmosphere; Stage #2: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In tetrahydrofuran at 20℃; for 5h; Inert atmosphere; | 80% |
4-dodecylaniline
4'-formyl-2-diphenylphosphino-acetophenone
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene for 2h; Heating; | 79% |
4-dodecylaniline
1,2-epox-[60]fullerene
A
1-(4-dodecylanilino)-2-hydroxy-1,2-dihydro[60]fullerene
B
5'-dodecylindolino[2',3':1,2][60]fullerene
Conditions | Yield |
---|---|
With sepiolite In chlorobenzene at 100℃; | A n/a B 78% |
1,3,5-trichloro-2,4,6-triazine
4-dodecylaniline
(4,6-Dichloro-[1,3,5]triazin-2-yl)-(4-dodecyl-phenyl)-amine
Conditions | Yield |
---|---|
With sodium hydroxide In water; acetone 1. 0 deg C, 1 h; 2. 20 deg C, 1 h; | 76% |
Conditions | Yield |
---|---|
With acetic acid | 76% |
Conditions | Yield |
---|---|
at 20℃; | 74% |
for 6h; Ambient temperature; |
4-dodecylaniline
Conditions | Yield |
---|---|
With benzyltriethylammonium tribromide; calcium carbonate In methanol; dichloromethane at 20℃; for 1h; | 74% |
With hydrogenchloride; bromine In water for 3h; |
Conditions | Yield |
---|---|
Stage #1: 4-dodecylaniline; Propiolic acid With dmap In tetrahydrofuran at 0℃; for 0.166667h; Inert atmosphere; Stage #2: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In tetrahydrofuran at 20℃; for 5h; Inert atmosphere; | 74% |
4-dodecylaniline
Conditions | Yield |
---|---|
With acetic acid In ethanol at 100℃; Inert atmosphere; | 73% |
4-dodecylaniline
2,3-bis(tert-butoxycarbonyl amino)propanoic acid
Conditions | Yield |
---|---|
Stage #1: 2,3-bis(tert-butoxycarbonyl amino)propanoic acid With 1-hydroxy-pyrrolidine-2,5-dione; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In chloroform at 20℃; for 2h; Inert atmosphere; Stage #2: 4-dodecylaniline With dmap In chloroform at 50℃; Inert atmosphere; | 72% |
4-dodecylaniline
N-Boc-D-serine(Bzl)-OH
[2-benzyloxy-1-(4-decyl-phenylcarbamoyl)-ethyl]-carbamic acid tert-butyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine | 71% |
4-dodecylaniline
Conditions | Yield |
---|---|
In neat (no solvent) Co complex mixed with ligand; heated on steam bath for 1 h; purified by preparative TLC (alumina, CHCl3); elem. anal.; | 70% |
1,4-bis(thiophen-2-yl)butane-1,4-dione
4-dodecylaniline
1-(p-dodecylphenyl)-2,5-di(2-thienyl)pyrrole
Conditions | Yield |
---|---|
In acetic acid; toluene at 140 - 150℃; | 69% |
4-dodecylaniline
2-bromo-4-dodecylaniline
Conditions | Yield |
---|---|
With N-Bromosuccinimide In dichloromethane at 20℃; for 20h; | 66% |
With sodium perborate; acetic acid; potassium bromide; sodium vanadate at 20℃; for 10h; | 59% |
With N-Bromosuccinimide; ammonium acetate In acetonitrile at 20℃; for 3h; |
4-dodecylaniline
1-dodecyl-4-iodobenzene
Conditions | Yield |
---|---|
With C5H11NO2; potassium iodide | 65% |
Stage #1: 4-dodecylaniline With hydrogenchloride; sodium nitrite at 0℃; Stage #2: With potassium iodide at 40℃; for 0.333333h; | 49% |
Conditions | Yield |
---|---|
Stage #1: 4-dodecylaniline With hydrogenchloride; sodium nitrite In tetrahydrofuran; water at 0℃; for 2h; Inert atmosphere; Stage #2: phenol With sodium carbonate; potassium carbonate In tetrahydrofuran; water at 20℃; for 12h; | 65% |
With hydrogenchloride; sodium carbonate; sodium nitrite In water | |
Stage #1: 4-dodecylaniline With hydrogenchloride; sodium nitrite In water at 0℃; for 0.5h; Stage #2: phenol With sodium carbonate In water at 0℃; for 1h; |
Product Name: 4-Dodecylaniline
The MF of 4-Dodecylaniline (104-42-7) is C18H31N.
The MW of 4-Dodecylaniline (104-42-7) is 261.45.
Synonyms of 4-Dodecylaniline (104-42-7): 4-Dodecylaniline ; p-Dodecylaniline ; 4-Dodecyl-benzenamin ; 4-N-Dodecylamine ; Benzenamine, 4-dodecyl-
Product Categories: Intermediates of Dyes and Pigments;Alkyl;Alkylanilines;Nitrogen Compounds;Organic Building Blocks;Polyamines
EINECS: 203-201-3
Index of Refraction: 1.508
Density: 0.902 g/ml
Flash Point: 162.7 °C
Boiling Point: 364 °C
Melting Point: 35-39 °C(lit.)
4-Dodecylaniline (104-42-7) is used for the manufacture of Kapu Lun Huang 3GS, Kapu Lun pink BS, Kapu Lun blue dye BS, etc.
Safety information of 4-Dodecylaniline (104-42-7):
Hazard Codes Xn
Risk Statements
22 Harmful if swallowed
Safety Statements
22 Do not breathe dust
24/25 Avoid contact with skin and eyes
WGK Germany 3
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