Conditions | Yield |
---|---|
With sodium hydrogensulfite |
Conditions | Yield |
---|---|
With hydrogenchloride; tin | |
With sodium sulfide |
Conditions | Yield |
---|---|
With sulfuric acid |
2-aminophenol-4-sulfonic acid
Conditions | Yield |
---|---|
With sodium sulfide; sodium hydroxide |
2-aminophenol-4-sulfonic acid
Conditions | Yield |
---|---|
With water; nickel at 70 - 100℃; Hydrogenation; |
acetic anhydride
2-aminophenol-4-sulfonic acid
3-acetamido-4-acetoxybenzenesulfonic acid
Conditions | Yield |
---|---|
With sulfuric acid In methanol for 4h; Reflux; | 97% |
With sulfuric acid In methanol for 4h; Reflux; | 97% |
With pyridine |
benzoyl chloride
2-aminophenol-4-sulfonic acid
3-benzoylamino-4-hydroxy-benzenesulfonic acid
Conditions | Yield |
---|---|
In water | 96.3% |
2-(trifluoromethyl)phenol
2-aminophenol-4-sulfonic acid
2-(2-hydroxyphenyl)benzo[d]oxazole-5-sulfonic acid
Conditions | Yield |
---|---|
With sodium hydroxide In water at 80℃; for 2h; | 92% |
Conditions | Yield |
---|---|
Stage #1: 2-aminophenol-4-sulfonic acid With water; sodium hydroxide; sodium nitrite at 0 - 5℃; for 0.0833333h; Stage #2: With hydrogenchloride; water at 0 - 5℃; for 0.5h; Stage #3: acetoacetamido With water; sodium acetate; sodium hydroxide In ethanol for 1h; | 86% |
Conditions | Yield |
---|---|
With 3,4,5-trihydroxybenzoic acid; cobalt(II) acetate; sodium hydroxide In water at 25℃; under 3000.3 Torr; for 36h; | 84% |
Conditions | Yield |
---|---|
With 3,4,5-trihydroxybenzoic acid; oxygen; manganese(II) acetate; sodium hydroxide In water at 25℃; under 2250.23 Torr; for 0.416667h; pH=10; Sonication; Autoclave; Green chemistry; regioselective reaction; | 72% |
2-aminophenol-4-sulfonic acid
4-benzoyl-1,5-diphenyl-1H-3-pyrazole carboxylic acid chloride
Conditions | Yield |
---|---|
With triethylamine In benzene for 10h; Heating; | 65% |
Conditions | Yield |
---|---|
Stage #1: 4-chloro-benzoyl chloride; 2-aminophenol-4-sulfonic acid at 180℃; for 14h; Stage #2: With thionyl chloride In chloroform Reflux; | 55% |
Conditions | Yield |
---|---|
With polyphosphoric acid at 140 - 180℃; | 54% |
2,3-dihydroxybenzonitrile
2-aminophenol-4-sulfonic acid
Conditions | Yield |
---|---|
With 3,4,5-trihydroxybenzoic acid; water; oxygen; manganese(II) acetate; sodium hydroxide at 25℃; under 2250.23 Torr; for 0.916667h; pH=10; Sonication; Autoclave; Green chemistry; regioselective reaction; | 52% |
2-aminophenol-4-sulfonic acid
2-hydroxyresorcinol
2,3,4,6'-tetrahydroxy-3'-sulfoazobenzene
Conditions | Yield |
---|---|
Stage #1: 2-aminophenol-4-sulfonic acid With hydrogenchloride In water at 0℃; Stage #2: With sodium nitrite In water at 0℃; for 2.5h; Stage #3: 2-hydroxyresorcinol With hydrogenchloride In water at 0℃; for 2.5h; pH=3; | 47.8% |
Conditions | Yield |
---|---|
With hydrogenchloride In water at 100℃; for 1h; Skraup Quinoline Synthesis; Inert atmosphere; | 39% |
2-hydroxy-N-phenylnaphthalene-1-carboxamide
2-aminophenol-4-sulfonic acid
C23H16N3O6S(1-)*Na(1+)
Conditions | Yield |
---|---|
Stage #1: 2-aminophenol-4-sulfonic acid With hydrogenchloride; sodium nitrite In water at -2 - 2℃; Stage #2: 2-hydroxy-N-phenylnaphthalene-1-carboxamide With sodium carbonate In water at 5 - 10℃; for 2h; | 35.4% |
Stage #1: 2-aminophenol-4-sulfonic acid With hydrogenchloride; sodium nitrite In water at -2 - 2℃; for 0.166667h; Stage #2: 2-hydroxy-N-phenylnaphthalene-1-carboxamide With sodium carbonate In water at 5 - 10℃; for 2h; | 35% |
Conditions | Yield |
---|---|
Stage #1: 2-aminophenol-4-sulfonic acid With hydrogenchloride; sodium nitrite In water at -2 - 2℃; for 0.166667h; Stage #2: 2,3-oxynaphthoic acid phenylamide With sodium carbonate In water at 5 - 10℃; for 2h; | 35.4% |
Conditions | Yield |
---|---|
With sodium hydroxide |
potassium thioacyanate
2-aminophenol-4-sulfonic acid
2-thioxo-2,3-dihydro-benzoxazole-5-sulfonic acid
Conditions | Yield |
---|---|
With water anschliessend Erhitzen auf 150grad; |
Conditions | Yield |
---|---|
With sodium carbonate |
Conditions | Yield |
---|---|
nachfolgend Reduktion; |
2-aminophenol-4-sulfonic acid
2-hydroxy-5-sulfo-benzenediazonium-betaine
Conditions | Yield |
---|---|
Diazotization; | |
With water; cis-nitrous acid | |
With nitrous anhydride | |
With water; nitrous anhydride |
2-aminophenol-4-sulfonic acid
2-oxo-2,3-dihydro-benzoxazole-5-sulfonic acid
Conditions | Yield |
---|---|
With sodium hydroxide |
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid at 0 - 3℃; |
2-aminophenol-4-sulfonic acid
2-amino-1-hydroxybenzene-4-sulphonic acid-N-phenylamide
Conditions | Yield |
---|---|
With phosphorus pentachloride Hinzufuegen von Anilin zu dem Reaktionsprodukt; |
phenylglyoxylic acid ethyl ester
2-aminophenol-4-sulfonic acid
2-oxo-3-phenyl-2H-benzo[1,4]oxazine-6-sulfonic acid
Conditions | Yield |
---|---|
With ammonium hydroxide In ethanol |
1-hydroxy-4-naphthalenesulfonate
2-aminophenol-4-sulfonic acid
C16H10N2O8S2(2-)*2Na(1+)
Conditions | Yield |
---|---|
With hydrogenchloride; sodium hydroxide; sodium carbonate; sodium chloride; sodium nitrite Multistep reaction; |
sodium resorcinol-4-sulphonate
2-aminophenol-4-sulfonic acid
C12H8N2O9S2(2-)*2Na(1+)
Conditions | Yield |
---|---|
With hydrogenchloride; sodium hydroxide; sodium carbonate; sodium chloride; sodium nitrite Multistep reaction; |
sodium 2-methylresorcinol-4-sulphonate
2-aminophenol-4-sulfonic acid
C13H10N2O9S2(2-)*2Na(1+)
Conditions | Yield |
---|---|
With hydrogenchloride; sodium hydroxide; sodium carbonate; sodium chloride; sodium nitrite 1b) 0 to 5 deg C, 2) 6 to 8 deg C, 1 d; Multistep reaction; |
The Benzenesulfonic acid,3-amino-4-hydroxy-, with the CAS registry number 98-37-3 and EINECS registry number 202-662-8, has the systematic name of 3-amino-4-hydroxybenzenesulfonic acid. It is a kind of brown crystals, and belongs to the proudct category of Intermediates of Dyes and Pigments. And the molecular formula of this chemical is C6H7NO4S.
The physical properties of Benzenesulfonic acid,3-amino-4-hydroxy- are as following: (1)ACD/LogP: -2.96; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -6.35; (4)ACD/LogD (pH 7.4): -6.5; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 1; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 5; (10)#H bond donors: 4; (11)#Freely Rotating Bonds: 3; (12)Polar Surface Area: 64.22 Å2; (13)Index of Refraction: 1.671; (14)Molar Refractivity: 42.24 cm3; (15)Molar Volume: 112.9 cm3; (16)Polarizability: 16.74×10-24cm3; (17)Surface Tension: 85.5 dyne/cm; (18)Density: 1.675 g/cm3.
You should be cautious while dealing with this chemical. It may cause burns. Therefore, you had better take the following instructions: Wear suitable protective clothing, gloves and eye/face protection, and in case of contacting with eyes, rinse immediately with plenty of water and seek medical advice; In case of accident or if you feel unwell, seek medical advice immediately (show label where possible).
You can still convert the following datas into molecular structure:
(1)SMILES: O=S(=O)(O)c1ccc(O)c(N)c1
(2)InChI: InChI=1/C6H7NO4S/c7-5-3-4(12(9,10)11)1-2-6(5)8/h1-3,8H,7H2,(H,9,10,11)
(3)InChIKey: ULUIMLJNTCECJU-UHFFFAOYAT
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