1,7-diacetoxynaphthalene
A
1,7-Dihydroxynaphthalene
Conditions | Yield |
---|---|
With lipase of Pseudomonas sp; water In various solvent(s) at 25℃; for 0.6h; Hydrolysis; deacetylation; | A n/a B n/a C 78% |
β-naphthol
A
2,6-Dihydroxynaphthalene
B
1,7-Dihydroxynaphthalene
C
1,6-dihydroxynaphthalene
D
2,7-Dihydroxynaphthalene
Conditions | Yield |
---|---|
With dihydrogen peroxide; hydrogen fluoride; antimony pentafluoride at -40℃; for 0.25h; Mechanism; Product distribution; | A 25.5% B 29% C 11% D 3.5% |
With dihydrogen peroxide; hydrogen fluoride; antimony pentafluoride at -40℃; for 0.25h; | A 25.5% B 29% C 11% D 3.5% |
Conditions | Yield |
---|---|
With dihydrogen peroxide; hydrogen fluoride; antimony pentafluoride at -20℃; for 0.5h; Mechanism; Product distribution; | A 17.5% B 25.5% |
With dihydrogen peroxide; hydrogen fluoride; antimony pentafluoride at -20℃; for 0.5h; | A 17.5% B 25.5% |
6-methoxy-1,4-dihydro-1,4-epoxidonaphthalene
1,7-Dihydroxynaphthalene
Conditions | Yield |
---|---|
With sodium hydride; ethanethiol In N,N-dimethyl-formamide at 130℃; for 7.5h; | 23% |
Conditions | Yield |
---|---|
With sulfuric acid at 200℃; | |
With hydrogenchloride at 200℃; | |
With phosphoric acid at 200℃; | |
With formic acid at 200℃; |
Conditions | Yield |
---|---|
With potassium hydroxide at 245 - 255℃; durch Verschmelzen; | |
With potassium hydroxide |
8-amino-2-naphthalenesulfonic acid
A
1,7-Dihydroxynaphthalene
B
8-amino-2-naphthol
C
8-hydroxy-naphthalene-2-sulfonic acid
Conditions | Yield |
---|---|
at 260℃; unter Druck; |
Conditions | Yield |
---|---|
With sulfuric acid at 200℃; | |
With hydrogenchloride at 200℃; | |
With phosphoric acid at 200℃; | |
With formic acid at 200℃; |
1,7-dihydroxy-2-naphthoic acid
1,7-Dihydroxynaphthalene
Conditions | Yield |
---|---|
With aniline |
Conditions | Yield |
---|---|
With hydrogen fluoride; boron trifluoride; dihydrogen peroxide at -50℃; for 0.5h; Mechanism; Product distribution; other naphthol, other temp.; |
1,7-Dihydroxynaphthalene
Conditions | Yield |
---|---|
With sulfuric acid at 200℃; | |
With hydrogenchloride at 200℃; | |
With phosphoric acid at 200℃; | |
With formic acid at 200℃; |
1,7-Dihydroxynaphthalene
Conditions | Yield |
---|---|
With sulfuric acid at 200℃; | |
With hydrogenchloride at 200℃; | |
With phosphoric acid at 200℃; | |
With formic acid at 200℃; |
1,7-Dihydroxynaphthalene
Conditions | Yield |
---|---|
With potassium hydroxide at 230℃; | |
With potassium hydroxide; sodium hydroxide at 230℃; |
Conditions | Yield |
---|---|
Verschmelzen; |
sulfuric acid
2-amino-8-hydroxy-naphthalene-3,6-disulphonic acid
1,7-Dihydroxynaphthalene
Conditions | Yield |
---|---|
at 200℃; |
1,7-dihydroxy-2-naphthoic acid
water
A
carbon dioxide
B
1,7-Dihydroxynaphthalene
Conditions | Yield |
---|---|
at 160℃; |
1,7-dihydroxy-2-naphthoic acid
aniline
A
carbon dioxide
B
1,7-Dihydroxynaphthalene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 22 percent / NaNH2, t-butyl alcohol / 2-methyl-propan-2-ol; tetrahydrofuran / 12 h / 55 °C 2: 23 percent / NaH, C2H5SH / dimethylformamide / 7.5 h / 130 °C View Scheme |
1,7-Dihydroxynaphthalene
magnesium methyl carbonate
1,7-dihydroxy-2-naphthoic acid
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 180℃; under 25857.4 Torr; for 6h; | 100% |
Conditions | Yield |
---|---|
With potassium hydroxide In water for 5h; | 98% |
With sodium hydroxide for 1h; Heating; | 96% |
With tetrabutylammomium bromide; potassium hydroxide In tetrahydrofuran; water at 0℃; | 95% |
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate; triethylamine In dichloromethane at 20℃; for 2h; | 96% |
trifluoromethylsulfonic anhydride
1,7-Dihydroxynaphthalene
naphthalene-1,7-diyl bis(trifluoromethanesulfonate)
Conditions | Yield |
---|---|
With pyridine | 95% |
With pyridine 1.) 0 deg C, 5 min, 2.) 0 deg C to r.t., 24 h; Yield given; |
1,7-Dihydroxynaphthalene
Conditions | Yield |
---|---|
With hydrogen fluoride | 95% |
1,7-Dihydroxynaphthalene
bispropargyl ether of 1,7-dihydroxynaphthalene
Conditions | Yield |
---|---|
91% |
3,5-bis((tetrahydro-2H-pyran-2-yl)oxy)benzoic acid
1,7-Dihydroxynaphthalene
Conditions | Yield |
---|---|
Stage #1: 3,5-bis((tetrahydro-2H-pyran-2-yl)oxy)benzoic acid With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine In dichloromethane at 20℃; for 0.25h; Stage #2: 1,7-Dihydroxynaphthalene In dichloromethane at 20℃; for 3h; | 91% |
Conditions | Yield |
---|---|
With methylene blue In methanol; water at 20℃; under 7500.75 Torr; for 0.266667h; Irradiation; Flow reactor; | 87% |
With oxone In water; acetonitrile at 20℃; for 10h; | 15% |
With methanol; potassium nitrososulfonate |
Conditions | Yield |
---|---|
With aluminum tri-bromide at 25℃; for 48h; | 87% |
Conditions | Yield |
---|---|
With pyridine for 3h; Inert atmosphere; | 86% |
at 100℃; | |
With pyridine at 100℃; |
1,7-Dihydroxynaphthalene
7-hydroxy-1-tetralone
Conditions | Yield |
---|---|
With aluminum tri-bromide; cyclohexane In various solvent(s) at 20℃; for 28h; Hydrogenation; | 83% |
With aluminum tri-bromide; cyclohexane In various solvent(s) at 25℃; for 24h; | 80% |
Conditions | Yield |
---|---|
With pyridine In tetrahydrofuran at 20℃; for 5h; | 83% |
1,7-Dihydroxynaphthalene
methyl iodide
1,7-dimethoxynaphthalen-2(1H)-one
Conditions | Yield |
---|---|
With potassium carbonate In butanone Heating / reflux; | 80% |
1,7-Dihydroxynaphthalene
3-(2-bromoacetyl)-4-hydroxyfuran-2(5H)-one
3,3'-{2,2'-[naphthalene-1,7-diylbis(oxy)]bis(acetyl)}bis[4-hydroxyfuran-2(5H)-one]
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 0 - 20℃; for 16h; | 79% |
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 85℃; for 1.5h; Inert atmosphere; | 79% |
With triethylamine In toluene at 35℃; for 10h; Inert atmosphere; Schlenk technique; |
1,7-Dihydroxynaphthalene
1,6-dihydroxynaphthalene
hexaethylphosphoric triamide
C28H32N2O4P2
Conditions | Yield |
---|---|
Stage #1: 1,7-Dihydroxynaphthalene; hexaethylphosphoric triamide In acetonitrile at 20℃; for 0.333333h; Stage #2: 1,6-dihydroxynaphthalene In acetonitrile at 20℃; for 48h; | 77% |
Conditions | Yield |
---|---|
With dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; acetic acid In 1,4-dioxane at 100℃; for 12h; Inert atmosphere; Schlenk technique; | 76% |
Conditions | Yield |
---|---|
With piperidine In ethanol for 1h; Heating; | 75% |
2,6-Dihydroxynaphthalene
1,7-Dihydroxynaphthalene
hexaethylphosphoric triamide
cyclo[(1,7-naphthylene)(2,6-naphthylene)-bis(diethyl phosphoramidite)]
Conditions | Yield |
---|---|
Stage #1: 1,7-Dihydroxynaphthalene; hexaethylphosphoric triamide In acetonitrile at 20℃; for 0.333333h; Stage #2: 2.6-dihydroxynaphthalene In acetonitrile at 20℃; for 48h; | 75% |
methanol
1,7-Dihydroxynaphthalene
A
1,7-dimethoxynaphthalene
B
7-methoxynaphth-1-ol
Conditions | Yield |
---|---|
With hydrogenchloride for 168h; Ambient temperature; | A n/a B 74% |
Conditions | Yield |
---|---|
In diethyl ether for 48h; Ambient temperature; | 73% |
1,7-Dihydroxynaphthalene
C35H20Cl2N4O4
Conditions | Yield |
---|---|
With cetyltrimethylammonim bromide In N,N-dimethyl-formamide Heating; | 73% |
thiosulfuric acid S-(2-amino-5-diethylamino-3-methylphenyl) ester
1,7-Dihydroxynaphthalene
Conditions | Yield |
---|---|
Stage #1: thiosulfuric acid S-(2-amino-5-diethylamino-3-methylphenyl) ester; 1,7-Dihydroxynaphthalene In dimethyl sulfoxide at 20℃; for 0.75h; Stage #2: With potassium dichromate In dimethyl sulfoxide at 20℃; for 0.333333h; Stage #3: With hydrogenchloride In methanol; water; dimethyl sulfoxide at 20℃; for 1h; | 73% |
thiosulfuric acid S-(2-amino-5-diethylamino-3-methylphenyl) ester
1,7-Dihydroxynaphthalene
Conditions | Yield |
---|---|
With potassium dichromate In dimethyl sulfoxide for 0.333333h; | 73% |
1,7-Dihydroxynaphthalene
4-Carboxybenzaldehyde
naphthalene-1,7-diyl bis(4-formylbenzoate)
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 48h; | 72% |
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 72h; | 51% |
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 72h; | 51% |
1,7-Dihydroxynaphthalene
2,7-Dihydroxynaphthalene
hexaethylphosphoric triamide
cyclo[(1,7-naphthylene)(2,7-naphthylene)-bis(diethyl phosphoramidite)]
Conditions | Yield |
---|---|
Stage #1: 1,7-Dihydroxynaphthalene; hexaethylphosphoric triamide In acetonitrile at 20℃; for 0.333333h; Stage #2: 2,7-Dihydroxynaphthalene In acetonitrile at 20℃; for 48h; | 71% |
1,7-Dihydroxynaphthalene
1,5-dihydroxynaphthalene
hexaethylphosphoric triamide
cyclo[(1,7-naphthylene)(1,5-naphthylene)-bis(diethyl phosphoramidite)]
Conditions | Yield |
---|---|
Stage #1: 1,7-Dihydroxynaphthalene; hexaethylphosphoric triamide In acetonitrile at 20℃; for 0.333333h; Stage #2: 1,5-dihydroxynaphthalene In acetonitrile at 20℃; for 48h; | 71% |
1,7-Dihydroxynaphthalene
3-(ethyl(3-hydroxy-4-nitrosophenyl)amino)propane-1-sulfonic acid hydrochloride
C21H20N2O6S
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 140℃; for 4h; Inert atmosphere; | 71% |
di(tert-butyl)chlorophosphine
1,7-Dihydroxynaphthalene
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran for 4h; Reflux; Inert atmosphere; | 71% |
With triethylamine In toluene at 35℃; for 10h; Inert atmosphere; Schlenk technique; |
Chemical Name: 1,7-Dihydroxynaphthalene
IUPAC NAME: naphthalene-1,7-diol
CAS No.: 575-38-2
EINECS: 209-383-0
RTECS: QJ4746666
RTECS Class:Mutagen
Molecular Formula: C10H8O2
Molecular Weight: 160.17 g/mol
Melting Point: 180-184 °C(lit.)
Density: 1.33 g/cm3
Flash Point: 193.5 °C
Boiling Point: 375.4 °C at 760 mmHg
1,7-NAPHTHALENEDIOL (575-38-2) is stable under normal temperatures and pressures.but incompatible with strong oxidizing agents.Following is the structure:
The chemical synonymous of 1,7-NAPHTHALENEDIOL (575-38-2) are c.i.76635 ; 1,7-DIHYDROXYNAPHTHALENE ; 1,7-NAPHTHALENEDIOL ; naphthalene-1,7-diol ; 1,7-Napthalenediol ; 1,7-NAPHTHALENEDIOL 97% ; 1,7-DihydroxylNaphthalene ; 1,7-Dihydroxynaphthalin
1. | mic-sat 1600 nmol/plate | MUREAV Mutation Research. 371 (1996),293. |
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