Conditions | Yield |
---|---|
With sulfur trioxide at 60℃; Temperature; Solvent; | 95.7% |
With dipyridinium dichromate; sodium hydrogensulfite In neat (no solvent) at 100℃; under 1500.15 Torr; for 0.0916667h; Reagent/catalyst; Microwave irradiation; | 75% |
With sulfuric acid; silica gel In 1,2-dichloro-ethane at 80℃; for 0.5h; | 60% |
Conditions | Yield |
---|---|
With sulfuric acid at 160 - 170℃; for 1.5h; | A 88.3% B 8.51% |
With sulfuric acid at 120℃; Product distribution; Rate constant; Thermodynamic data; activation energy; microwave or irradiation; regioselectivity; | |
With sulfuric acid at 120℃; for 0.5h; Product distribution; microwave activation; various power, temperature, reaction time, H2SO4 concentration; |
Conditions | Yield |
---|---|
Stage #1: 1-Naphthalenesulfonyl chloride With N-ethyl-N,N-diisopropylamine; Wang resin In dichloromethane at 22℃; Stage #2: With trifluoroacetic acid In dichloromethane for 1h; Further stages.; | 85% |
With sodium hydrogencarbonate In water at 80 - 90℃; | 0.25 g |
With water In acetone at 30℃; Kinetics; Mechanism; Thermodynamic data; other temperatures; ΔH(excit.), ΔS(excit.); various concentrations of the reagent and substrate; | |
Multi-step reaction with 2 steps 1: alcohol; zinc 2: water View Scheme |
Conditions | Yield |
---|---|
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; caesium carbonate; Aminoiminomethanesulfinic acid In dimethyl sulfoxide at 100℃; for 14h; Green chemistry; | 71% |
Conditions | Yield |
---|---|
With chlorosulphuric acid; benzene |
Conditions | Yield |
---|---|
With tetrachloromethane; chlorosulfonic acid at -5℃; |
naphthalene-1-sulphinic acid
A
1-naphthalenesulfonic acid
B
S-(naphthalen-1-yl) naphthalene-1-sulfonothioate
Conditions | Yield |
---|---|
With water |
naphthalene-1-sulfonic acid menthyl ester
A
1-naphthalenesulfonic acid
B
3-p-menthene
Conditions | Yield |
---|---|
under 4 Torr; bei der Destillation.Thermolysis; naphthalene-1-sulfonic acid l-menthyl ester; |
naphthalene
A
naphthalene-2-sulfonate
B
1-naphthalenesulfonic acid
C
naphthalene-1,7-disulphonic acid
D
naphthalene-1,6-disulfonic acid
E
naphthalene-1,5-disulfonate
Conditions | Yield |
---|---|
With sulfur trioxide; water Product distribution; multistep reaction; various reaction conditions; |
naphthalene
A
naphthalene-2-sulfonate
B
1-naphthalenesulfonic acid
C
naphthalene-1,6-disulfonic acid
D
naphthalene-1,5-disulfonate
Conditions | Yield |
---|---|
With sulfur trioxide; water 1.) CH2Cl2, 22 deg C, 60 min, 2.) 70 - 80 deg C, 30 min; Multistep reaction. Further byproducts given. Title compound not separated from byproducts; |
Conditions | Yield |
---|---|
at 80℃; |
naphthalene
sulfuric acid
sulfur trioxide
1-naphthalenesulfonic acid
naphthalene
sulfuric acid
boron trifluoride
water
1-naphthalenesulfonic acid
chlorosulfonic acid
naphthalene
benzene
1-naphthalenesulfonic acid
Conditions | Yield |
---|---|
je ein Mol von Verb. 1 und 2; | |
je ein Mol von Verb. 1 und 2; |
naphthalene
sulfuric acid
A
naphthalene-2-sulfonate
B
1-naphthalenesulfonic acid
Conditions | Yield |
---|---|
at 1℃; Product distribution; und 57grad; |
Conditions | Yield |
---|---|
at 170℃; | |
at 170℃; |
chlorosulfonic acid
naphthalene
A
naphthalene-2-sulfonate
B
1-naphthalenesulfonic acid
Conditions | Yield |
---|---|
at 100℃; nach Entfernen des CS2; |
tetrachloromethane
chlorosulfonic acid
naphthalene
A
1-naphthalenesulfonic acid
B
1-Naphthalenesulfonyl chloride
Conditions | Yield |
---|---|
at -15 - -5℃; mit 2 Mol von Verb. 1; |
naphthalene
sulfuric acid
A
1-naphthalenesulfonic acid
B
naphthalene-1,7-disulphonic acid
C
naphthalene-1,6-disulfonic acid
D
naphthalene-1,5-disulfonate
Conditions | Yield |
---|---|
at 40℃; Product distribution; |
Conditions | Yield |
---|---|
With sulfuric acid at 393℃; Kinetics; Rate constant; |
1-naphthalenesulfonic acid
Conditions | Yield |
---|---|
at 110℃; |
naphthalene-1-sulphinic acid
water
A
1-naphthalenesulfonic acid
B
S-(naphthalen-1-yl) naphthalene-1-sulfonothioate
4-iodo-naphthalene-1-sulfonic acid
water
copper(II) sulfate
1-naphthalenesulfonic acid
Conditions | Yield |
---|---|
der Kalium-Salz reagiert; |
Conditions | Yield |
---|---|
der Kalium-Salz reagiert; |
Conditions | Yield |
---|---|
der Kalium-Salz reagiert; |
Conditions | Yield |
---|---|
der Kalium-Salz reagiert; |
A
1-naphthalenesulfonic acid
B
S-(naphthalen-1-yl) naphthalene-1-sulfonothioate
benzoyl-(naphthalene-1-sulfonyl)-amine
A
1-naphthalenesulfonic acid
B
benzoic acid
1-naphthalenesulfonic acid
naphthalene-1-sulfonyl azide
Conditions | Yield |
---|---|
Stage #1: 1-naphthalenesulfonic acid With trichloroisocyanuric acid; triphenylphosphine In tetrahydrofuran at 0 - 5℃; Stage #2: With sodium azide In tetrahydrofuran at 5 - 20℃; | 97% |
With sodium azide; trichloroacetonitrile; triphenylphosphine In acetonitrile at 20℃; for 0.5h; | 89% |
1-naphthalenesulfonic acid
N,N-dimethyl-formamide
m,p-dichloroaniline
N-(3,4-dichlorophenyl)-1-naphthalene carboxamide
Conditions | Yield |
---|---|
Stage #1: 1-naphthalenesulfonic acid; N,N-dimethyl-formamide With oxalyl dichloride In dichloromethane at 20℃; for 2h; Stage #2: m,p-dichloroaniline With oxalyl dichloride; triethylamine In dichloromethane at 20℃; for 2h; | 96% |
1-naphthalenesulfonic acid
m-toluidine hydrochloride
N,N-dimethyl-formamide
N-(3-methylphenyl)-1-naphthalene carboxamide
Conditions | Yield |
---|---|
Stage #1: 1-naphthalenesulfonic acid; N,N-dimethyl-formamide With oxalyl dichloride In dichloromethane at 20℃; for 2h; Stage #2: m-toluidine hydrochloride With oxalyl dichloride; triethylamine In dichloromethane at 20℃; for 2h; Cooling with ice; | 96% |
Conditions | Yield |
---|---|
With silver hexafluoroantimonate; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; copper(II) acetate monohydrate In N,N-dimethyl-formamide at 120℃; for 16h; Inert atmosphere; diastereoselective reaction; | 91% |
methyl (2-cyanoethyl)acetoacetate
1-naphthalenesulfonic acid
ethylene glycol
ethyl 4-cyano-2-(2-methyl-1,3-dioxolan-2-yl)butanoate
Conditions | Yield |
---|---|
In toluene | 89% |
1-naphthalenesulfonic acid
1-azido-2-(phenylethynyl)benzene
Conditions | Yield |
---|---|
With palladium diacetate In 1,4-dioxane at 60℃; for 2h; | 87% |
Benzyl isocyanide
1-naphthalenesulfonic acid
naphthalene-1-sulfonic acid benzylamide
Conditions | Yield |
---|---|
With water In dichloromethane at 20℃; for 0.333333h; | 86% |
1-naphthalenesulfonic acid
Conditions | Yield |
---|---|
In ethanol at 80℃; for 1h; | 82.4% |
1-naphthalenesulfonic acid
Conditions | Yield |
---|---|
Stage #1: 1-naphthalenesulfonic acid With hydrogenchloride; p-toluidine In water at 0℃; for 4h; Inert atmosphere; Stage #2: With n-butyllithium In tetrahydrofuran; hexane at -40 - 20℃; for 12h; Inert atmosphere; | 80% |
1-naphthalenesulfonic acid
1,1’-bis(phenylmethyl)-4,4’bipyridinium bromide
Conditions | Yield |
---|---|
In water | 79% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane ice-cooling; | 78% |
((2S,4S)-4-(4-(3-methyl-1-phenyl-1H-pyrazol-5-yl)piperazin-1-yl)pyrrolidin-2-yl)(1,3-thiazolidin-3-yl)methanone
1-naphthalenesulfonic acid
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 3h; | 75% |
Conditions | Yield |
---|---|
With phosphorus pentachloride; sodium chloride 1.) pH=neutral with sodium hydrogen carbonate, water, reflux; 2.) 170-180 deg C, 3 h; | 68% |
With thionyl chloride In diethyl ether Ambient temperature; |
Conditions | Yield |
---|---|
With (R)-2-(tert-butylsulfonyl)-6-chloro-2′-iodo-1,1′-biphenyl; 3-chloro-benzenecarboperoxoic acid In ethyl acetate at 20℃; for 72h; Inert atmosphere; enantioselective reaction; | 68% |
1-naphthalenesulfonic acid
prasugel
prasugrel 1-naphthalenesulfonic acid salt
Conditions | Yield |
---|---|
In acetone at 20℃; for 0.333333h; | 66% |
In acetone at 20℃; |
Conditions | Yield |
---|---|
With 2-Iodobenzoic acid; iodine; 3-chloro-benzenecarboperoxoic acid In acetonitrile at 50℃; for 8h; Darkness; | 65% |
Conditions | Yield |
---|---|
With (R)-2-(tert-butylsulfonyl)-6-chloro-2′-iodo-1,1′-biphenyl; 3-chloro-benzenecarboperoxoic acid In ethyl acetate at 20℃; for 72h; Inert atmosphere; enantioselective reaction; | 65% |
1-naphthalenesulfonic acid
Conditions | Yield |
---|---|
In acetone at 40℃; for 0.0833333h; Schlenk technique; Inert atmosphere; | 63% |
Conditions | Yield |
---|---|
With (R)-2-(tert-butylsulfonyl)-6-chloro-2′-iodo-1,1′-biphenyl; 3-chloro-benzenecarboperoxoic acid In ethyl acetate at 20℃; for 72h; Inert atmosphere; enantioselective reaction; | 63% |
Conditions | Yield |
---|---|
With silver hexafluoroantimonate; dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; silver(I) acetate In 1,4-dioxane at 100℃; for 16h; Sealed tube; Inert atmosphere; Schlenk technique; | 62% |
1-naphthalenesulfonic acid
ethyl 5-hydroxy-5-phenylpenta-2,3-dienoate
Conditions | Yield |
---|---|
In chloroform at 25℃; Inert atmosphere; stereoselective reaction; | 58% |
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; palladium diacetate In dichloromethane at 60℃; for 24h; Inert atmosphere; Sealed tube; stereoselective reaction; | 56% |
Conditions | Yield |
---|---|
With (2R,2'R)-2,2'-([2-iodo-1,3-phenylene]bis(oxy))bis(N-mesitylpropanamide); 3-chloro-benzenecarboperoxoic acid In diethyl ether; 2,2,2-trifluoroethanol at -45 - 20℃; for 120h; Solvent; Temperature; enantioselective reaction; | A 35% B n/a |
Conditions | Yield |
---|---|
With H2O2 In not given | 25% |
With H2O2 In diethyl ether react. mixt. treated with 30% aq. H2O2, kept at 20°C for 12 h; evapd., recrystd. (toluene), elem. anal.; | 25% |
Product Name: 1-Naphthalenesulfonic acid (CAS NO.85-47-2)
Molecular Formula: C10H8O3S
Molecular Weight: 208.23g/mol
Mol File: 85-47-2.mol
Einecs: 201-610-1
Melting Point: 77-79 °C(lit.)
Density: 1.423 g/cm3
Water Solubility: freely soluble
Product Categories: Intermediates of Dyes and Pigments ; Organic Building Blocks ; Sulfonic/Sulfinic Acids ; Sulfur Compounds
Synonyms of 1-Naphthalenesulfonic acid (CAS NO.85-47-2): 1-Naphthyl sulfonic acid ; Sulfonated naphthalene ; Naphthalene-1-sulfonic acid ; Alpha napthalene sulphonate ; Alpha-naphthalenesulfonic acid ; 1-Naphthalenesulfonic acid ; 1-Naphthalenesulfonic acid, dihydrate ; Naphthalene-1-sulfonic acid dihydrate .
Safety Information of 1-Naphthalenesulfonic acid (CAS NO.85-47-2):
Hazard Codes: C,F
Risk Statements: 34-11
11: Highly Flammable
34: Causes burns
Safety Statements: 26-36/37/39-45-28-16
16: Keep away from sources of ignition - No smoking
26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
28: After contact with skin, wash immediately with plenty of ... (to be specified by the manufacturer)
36: Wear suitable protective clothing
37: Wear suitable gloves
39: Wear eye/face protection
45: In case of accident or if you feel unwell, seek medical advice immediately (show label where possible)
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