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86-48-6 Usage

Uses

Different sources of media describe the Uses of 86-48-6 differently. You can refer to the following data:
1. Metabolite from phenanthrene degradation.
2. It is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuff.

General Description

1-Hydroxy-2-naphthoic acid is produced by the transformation of phenanthrene by NCIB 9816 clones.

Purification Methods

Successively crystallise the acid from EtOH/water, diethyl ether and acetonitrile, with filtration through a column of charcoal and Celite. [Tong & Glesmann J Am Chem Soc 79 583 1957, Beilstein 10 H 331, 10 IV 1194.]

Check Digit Verification of cas no

The CAS Registry Mumber 86-48-6 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86-48:
(4*8)+(3*6)+(2*4)+(1*8)=66
66 % 10 = 6
So 86-48-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H8O3/c12-10-8-4-2-1-3-7(8)5-6-9(10)11(13)14/h1-6,12H,(H,13,14)/p-1

86-48-6 Well-known Company Product Price

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  • Alfa Aesar

  • (A12785)  1-Hydroxy-2-naphthoic acid, 98+%   

  • 86-48-6

  • 250g

  • 565.0CNY

  • Detail
  • Alfa Aesar

  • (A12785)  1-Hydroxy-2-naphthoic acid, 98+%   

  • 86-48-6

  • 500g

  • 1015.0CNY

  • Detail
  • Alfa Aesar

  • (A12785)  1-Hydroxy-2-naphthoic acid, 98+%   

  • 86-48-6

  • 1000g

  • 1822.0CNY

  • Detail

86-48-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Hydroxy-2-naphthoic acid

1.2 Other means of identification

Product number -
Other names 2-Naphthalenecarboxylic acid, 1-hydroxy-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:86-48-6 SDS

86-48-6Synthetic route

α-naphthol
90-15-3

α-naphthol

magnesium methyl carbonate
4861-79-4

magnesium methyl carbonate

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 180℃; under 25857.4 Torr; for 6h;96%
α-naphthol
90-15-3

α-naphthol

sodium ethyl carbonate
17201-44-4

sodium ethyl carbonate

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
at 140 - 190℃; under 7600 Torr; for 5h;93.4%
α-naphthol
90-15-3

α-naphthol

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
With potassium hydrogencarbonate at 200℃; for 5h;60%
With salicylic acid decarboxylase from Trichosporon moniliiforme; potassium hydrogencarbonate In acetonitrile at 30℃; for 24h; pH=8.5; aq. phosphate buffer; Enzymatic reaction; regioselective reaction;
Multi-step reaction with 4 steps
1.1: 1H-imidazole / N,N-dimethyl-formamide / 0.5 h / 0 - 20 °C / Inert atmosphere
1.2: 0 - 20 °C / Inert atmosphere
2.1: water; sodium hydrogencarbonate / N,N-dimethyl-formamide; diethyl ether / 0.5 h / 20 °C / Inert atmosphere
3.1: palladium diacetate; silver(I) acetate; N-tert-butoxycarbonyl-L-leucine; 2,2,2-trifluoroethanol / 1,2-dichloro-ethane / 0.08 h / 95 °C / Inert atmosphere
3.2: 18 h / 95 °C / Inert atmosphere
4.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / Inert atmosphere
View Scheme
1-methyl-4-nitrosobenzene
623-11-0

1-methyl-4-nitrosobenzene

4-isopropyl-benzo[h]chromen-2-one
858438-04-7

4-isopropyl-benzo[h]chromen-2-one

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

1-nitro-naphthalene-2-carbonitrile
1885-78-5

1-nitro-naphthalene-2-carbonitrile

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
With barium dihydroxide
3-acetyl-2-methyl-benzo[h]chromen-4-one
69796-59-4

3-acetyl-2-methyl-benzo[h]chromen-4-one

furan-2,3,5(4H)-trione pyridine (1:1)

furan-2,3,5(4H)-trione pyridine (1:1)

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

1-hydroxynaphthalene-2-carbonitrile
67176-26-5

1-hydroxynaphthalene-2-carbonitrile

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
With alkaline solution
sodium naphtholate
3019-88-3

sodium naphtholate

methylammonium carbonate
15719-64-9, 15719-76-3, 97762-63-5

methylammonium carbonate

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
With 1,4-dioxane
With pyridine
2-cyano-naphthalene-1-sulfonic acid ; sodium-salt

2-cyano-naphthalene-1-sulfonic acid ; sodium-salt

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
at 200 - 220℃; In der Kalischmelze;
3-benzoyl-5-chloromethyl-dihydro-furan-2-one
104095-33-2

3-benzoyl-5-chloromethyl-dihydro-furan-2-one

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
With aluminium trichloride
phosgene
75-44-5

phosgene

α-naphthol
90-15-3

α-naphthol

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
Yield given. Multistep reaction;
2-(diethylamino)-4H-naphtho[1,2-b]pyran-4-one
61035-03-8

2-(diethylamino)-4H-naphtho[1,2-b]pyran-4-one

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
With potassium hydroxide In ethanol Heating;
6-Diazo-benzocycloheptene-5,7-dione
28591-61-9

6-Diazo-benzocycloheptene-5,7-dione

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
With water
1-hydroxy-2-naphthaldehyde
574-96-9

1-hydroxy-2-naphthaldehyde

A

2-(hydroxymethyl)-1-naphthol
59648-32-7

2-(hydroxymethyl)-1-naphthol

B

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
With barium dihydroxide; formaldehyd at 100 - 110℃; for 4h;A 85 % Chromat.
B 9 % Chromat.
3-ethyl-2-methyl-benzo[h]chromen-4-one
875224-19-4

3-ethyl-2-methyl-benzo[h]chromen-4-one

aqueous alkaline solution

aqueous alkaline solution

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

3-acetyl-benzo[h]chromene-2,4-dione

3-acetyl-benzo[h]chromene-2,4-dione

KOH-solution

KOH-solution

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

2,4-dioxo-3,4-dihydro-2H-benzo[h]chromene-3-carboxylic acid ethyl ester

2,4-dioxo-3,4-dihydro-2H-benzo[h]chromene-3-carboxylic acid ethyl ester

KOH-solution

KOH-solution

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

3-benzyl-4-methyl-benzo[h]chromen-2-one
95703-28-9

3-benzyl-4-methyl-benzo[h]chromen-2-one

KOH-solution

KOH-solution

A

4-Phenyl-2-butanone
2550-26-7

4-Phenyl-2-butanone

B

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

4-methyl-3-phenyl-benzo[h]chromen-2-one
861353-04-0

4-methyl-3-phenyl-benzo[h]chromen-2-one

KOH-solution

KOH-solution

A

2-methyl-benzeneacetaldehyde
10166-08-2

2-methyl-benzeneacetaldehyde

B

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

aluminium trichloride
7446-70-0

aluminium trichloride

3-benzoyl-5-chloromethyl-dihydro-furan-2-one
104095-33-2

3-benzoyl-5-chloromethyl-dihydro-furan-2-one

benzene
71-43-2

benzene

A

phenyl(1,2,3,4-tetrahydronaphthalen-1-yl)methanone
94540-41-7

phenyl(1,2,3,4-tetrahydronaphthalen-1-yl)methanone

B

1,4,5-triphenyl-pentan-1-one
112863-69-1

1,4,5-triphenyl-pentan-1-one

C

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

α-naphthol
90-15-3

α-naphthol

carbon dioxide
124-38-9

carbon dioxide

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
With sodium
With sodium; toluene
With potassium carbonate under 36775.4 Torr;
With potassium hydrogencarbonate; glycerol
1-oxy-3.4-dihydro-naphthoic acid-(2)-ethyl ester

1-oxy-3.4-dihydro-naphthoic acid-(2)-ethyl ester

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
With sodium; sodium cyclohexanolate; cyclohexanol at 190 - 200℃;
carbon dioxide
124-38-9

carbon dioxide

sodium naphtholate
3019-88-3

sodium naphtholate

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
at 135℃;
carbon dioxide
124-38-9

carbon dioxide

alkali-α-naphtholate

alkali-α-naphtholate

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
With alkali sulfite
methylammonium carbonate
15719-64-9, 15719-76-3, 97762-63-5

methylammonium carbonate

alkali salt of α-naphthol

alkali salt of α-naphthol

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
Erhitzen des entstandenen Salzes im Autoklaven auf 120-140grad;
Erhitzen des entstandenen Salzes im Autoklaven auf 120-140grad;
sodium salt of/the/ 2-cyano-naphthalene-sulfonic acid-(1)

sodium salt of/the/ 2-cyano-naphthalene-sulfonic acid-(1)

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
at 200 - 220℃; durch Kalischmelze;
α-naphthol
90-15-3

α-naphthol

carbon dioxide
124-38-9

carbon dioxide

sodium

sodium

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

α-naphthol
90-15-3

α-naphthol

carbon dioxide
124-38-9

carbon dioxide

toluene
108-88-3

toluene

sodium

sodium

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

1-nitro-naphthalene-2-carbonitrile
1885-78-5

1-nitro-naphthalene-2-carbonitrile

aq. barium hydroxide solution

aq. barium hydroxide solution

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

dimethyl sulfate
77-78-1

dimethyl sulfate

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

1-hydroxy-naphthalene-2-carboxylic acid methyl ester
948-03-8

1-hydroxy-naphthalene-2-carboxylic acid methyl ester

Conditions
ConditionsYield
With lithium hydroxide In tetrahydrofuran for 1h; Methylation; esterification; Heating;100%
Stage #1: 1-hydroxy-2-naphthoic acid With lithium hydroxide In tetrahydrofuran for 0.5h;
Stage #2: dimethyl sulfate In tetrahydrofuran for 3h; Heating;
95.9%
Stage #1: 1-hydroxy-2-naphthoic acid With triethylamine In acetone for 0.25h; Inert atmosphere;
Stage #2: dimethyl sulfate In acetone at 55℃; for 12h; Inert atmosphere;
95%
methyl iodide
74-88-4

methyl iodide

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

methyl 1-methoxy-2-naphthoate
6039-59-4

methyl 1-methoxy-2-naphthoate

Conditions
ConditionsYield
With potassium carbonate In acetone Reflux;100%
With potassium carbonate In acetone Reflux;96%
With potassium carbonate In acetone for 18h; Reflux;95%
meloxicam
71125-38-7

meloxicam

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

4-hydroxy-2-methyl-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide 1-hydroxy-2-naphthoic acid (1:1)
1174325-92-8

4-hydroxy-2-methyl-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide 1-hydroxy-2-naphthoic acid (1:1)

Conditions
ConditionsYield
In tetrahydrofuran for 0.5h;100%
In tetrahydrofuran Product distribution / selectivity;
In dimethylsulfoxide-d6; water at 25 - 90℃; Solvent;71 g
camostat
59721-28-7

camostat

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

N,N-dimethyl-carbamoylmethyl p-(p-guanidinobenzoyloxy)phenylacetate xinafoate

N,N-dimethyl-carbamoylmethyl p-(p-guanidinobenzoyloxy)phenylacetate xinafoate

Conditions
ConditionsYield
In water; isopropyl alcohol at 25 - 60℃;99.1%
1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

4-bromo-1-hydroxy-2-naphthoic acid
5813-37-6

4-bromo-1-hydroxy-2-naphthoic acid

Conditions
ConditionsYield
With bromine In acetic acid at 20℃;99%
With bromine; acetic acid at 20℃;99%
With bromine In acetic acid at 20℃; Inert atmosphere;92%
propan-1-ol
71-23-8

propan-1-ol

zirconium tetrapropoxide
23519-77-9

zirconium tetrapropoxide

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

Zr6O2(OC3H7)16(O2CC10H6O)2(C3H7OH)2

Zr6O2(OC3H7)16(O2CC10H6O)2(C3H7OH)2

Conditions
ConditionsYield
In propan-1-ol (argon); storing in a Schlenk tube (ambient temp., 14 d);99%
2-aminonaphthalenesulfonic acid
81-16-3

2-aminonaphthalenesulfonic acid

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

A

2-[(1-hydroxy-2-naphthalenyl)azo]-1-naphthalenesulfonic acid sodium salt
1402066-96-9

2-[(1-hydroxy-2-naphthalenyl)azo]-1-naphthalenesulfonic acid sodium salt

B

1-hydroxy-4-[(1-sulfo-2-naphthalenyl)azo]-2-naphthalenecarboxylic acid disodium salt

1-hydroxy-4-[(1-sulfo-2-naphthalenyl)azo]-2-naphthalenecarboxylic acid disodium salt

Conditions
ConditionsYield
Stage #1: 2-aminonaphthalenesulfonic acid With hydrogenchloride; sodium hydroxide; sodium nitrite In water at 0℃; for 0.5h;
Stage #2: 1-hydroxy-2-naphthoic acid With sodium carbonate In ethanol; water at 0℃;
A 12%
B 97%
1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

1-acetoxy-2-naphthoic acid
6301-40-2

1-acetoxy-2-naphthoic acid

Conditions
ConditionsYield
With sulfuric acid In acetic anhydride at 100℃; for 0.166667h;97%
dimethyl sulfate
77-78-1

dimethyl sulfate

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

methyl 1-methoxy-2-naphthoate
6039-59-4

methyl 1-methoxy-2-naphthoate

Conditions
ConditionsYield
With potassium carbonate In acetone at 50℃; Temperature;96%
Stage #1: 1-hydroxy-2-naphthoic acid With potassium carbonate In acetone for 0.25h; Inert atmosphere;
Stage #2: dimethyl sulfate In acetone at 55℃; for 12h; Inert atmosphere;
95%
With potassium carbonate In acetone Heating;
With potassium carbonate In acetone for 8h; Reflux;
1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

A

9-methoxy-2-amino-1,2,3,4-tetrahydroanthracene
179041-74-8

9-methoxy-2-amino-1,2,3,4-tetrahydroanthracene

B

10-methoxy-2-amino-1,2,3,4-tetrahydrophenanthrene
179041-75-9

10-methoxy-2-amino-1,2,3,4-tetrahydrophenanthrene

Conditions
ConditionsYield
A 95%
B n/a
3,6-diazabicyclo[3.1.1]heptan-3-yl(cyclopropyl) methanone
1310717-02-2

3,6-diazabicyclo[3.1.1]heptan-3-yl(cyclopropyl) methanone

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

C9H14N2O*C11H8O3
1400593-10-3

C9H14N2O*C11H8O3

Conditions
ConditionsYield
In Isopropyl acetate; water at 60℃;95%
(R)-N-(3-(5-fluoro-2-(2-fluoro-3-(methylsulfonyl)phenylamino)pyrimidin-4-yl)-1H-indol-7-yl)-3-methoxy-2-(4-methylpiperazin-1-yl)propanamide

(R)-N-(3-(5-fluoro-2-(2-fluoro-3-(methylsulfonyl)phenylamino)pyrimidin-4-yl)-1H-indol-7-yl)-3-methoxy-2-(4-methylpiperazin-1-yl)propanamide

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

(R)-N-(3-(5-fluoro-2-((2-fluoro-3-(methylsulfonyl)phenyl)amino)pyrimidin-4-yl)-1H-indol-7-yl)-3-methoxy-2-(4-methylpiperazin-1-yl)propanamide xinafoic acid

(R)-N-(3-(5-fluoro-2-((2-fluoro-3-(methylsulfonyl)phenyl)amino)pyrimidin-4-yl)-1H-indol-7-yl)-3-methoxy-2-(4-methylpiperazin-1-yl)propanamide xinafoic acid

Conditions
ConditionsYield
Stage #1: (R)-N-(3-(5-fluoro-2-(2-fluoro-3-(methylsulfonyl)phenylamino)pyrimidin-4-yl)-1H-indol-7-yl)-3-methoxy-2-(4-methylpiperazin-1-yl)propanamide In methanol; ethyl acetate at 65℃; Inert atmosphere;
Stage #2: 1-hydroxy-2-naphthoic acid In methanol; ethyl acetate at 50℃; Inert atmosphere;
95%
salmeterol
89365-50-4

salmeterol

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

salmeterol xinafoate

salmeterol xinafoate

Conditions
ConditionsYield
In acetone at 30℃; for 0.666667h; Temperature; Solvent;94.1%
In acetone at 25 - 45℃; for 1.5h;69%
In diethyl ether at 20℃; for 16h;
In isopropyl alcohol
Stage #1: salmeterol With pyrographite In methanol at 25 - 30℃; for 0.5h;
Stage #2: 1-hydroxy-2-naphthoic acid In methanol at 18 - 30℃; for 3h;
20.75 g
formaldehyd
50-00-0

formaldehyd

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

4,4'-methylenebis(1-hydroxy-2-naphthoic acid)
1175-41-3

4,4'-methylenebis(1-hydroxy-2-naphthoic acid)

Conditions
ConditionsYield
With sulfuric acid 1.) 90 deg C, 6 h, 2.) RT, 12 h;94%
ethanol
64-17-5

ethanol

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

ethyl 1-hydroxy-2-naphthoate
33950-71-9

ethyl 1-hydroxy-2-naphthoate

Conditions
ConditionsYield
With pyridine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In toluene at 20℃; for 7.5h; Inert atmosphere;93%
With sulfuric acid
Stage #1: 1-hydroxy-2-naphthoic acid With thionyl chloride
Stage #2: ethanol With triethylamine
With sulfuric acid Reflux;
dimethyl sulfate
77-78-1

dimethyl sulfate

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

1-methoxy-2-naphthoic acid
883-21-6

1-methoxy-2-naphthoic acid

Conditions
ConditionsYield
Stage #1: dimethyl sulfate; 1-hydroxy-2-naphthoic acid With potassium carbonate
Stage #2: With lithium hydroxide In tetrahydrofuran; water
92%
With sodium hydroxide In water
5,5-dibenzyl-2,3,4,5-tetrahydropyridine
1416767-53-7

5,5-dibenzyl-2,3,4,5-tetrahydropyridine

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

12,12-dibenzyl-10,11,12,12a-tetrahydronaphtho[2,1-e]pyrido[2,1-b][1,3]oxazin-7(9H)-one
1416767-44-6

12,12-dibenzyl-10,11,12,12a-tetrahydronaphtho[2,1-e]pyrido[2,1-b][1,3]oxazin-7(9H)-one

Conditions
ConditionsYield
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine In toluene at 90℃; for 20h; Inert atmosphere;92%
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine In toluene at 90℃; for 20h;92%
benzyl bromide
100-39-0

benzyl bromide

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

1-benzyloxynaphthalene-2-carboxylic acid

1-benzyloxynaphthalene-2-carboxylic acid

Conditions
ConditionsYield
With potassium carbonate; tetrabutylammomium bromide In tetrahydrofuran at 30℃; for 0.166667h;91%
methanol
67-56-1

methanol

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

1-hydroxy-naphthalene-2-carboxylic acid methyl ester
948-03-8

1-hydroxy-naphthalene-2-carboxylic acid methyl ester

Conditions
ConditionsYield
With sulfuric acid90%
With sulfuric acid90%
With sulfuric acid at 80℃; for 8h;80%
1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

ethyl 1-hydroxy-2-naphthoate
33950-71-9

ethyl 1-hydroxy-2-naphthoate

Conditions
ConditionsYield
With ethanol; sulfuric acid for 8h; Reflux;90%
Multi-step reaction with 2 steps
1: SOCl2 / tetrahydrofuran / 2 h / 20 °C
2: 88 percent / 0.17 h / 120 °C / microwave irradiation
View Scheme
Multi-step reaction with 2 steps
1: petroleum ether; thionyl chloride
View Scheme
1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

2-chloro-4H-naphtho[1,2-d][1,3,2]dioxaphosphinin-4-one
352662-32-9

2-chloro-4H-naphtho[1,2-d][1,3,2]dioxaphosphinin-4-one

Conditions
ConditionsYield
With triethylamine; phosphorus trichloride In toluene at 20℃;90%
With anhydrous phosphorus trichloride In toluene75%
With Lewatit MP-62; phosphorus trichloride In toluene at 20℃; Product distribution / selectivity;75%
With triethylamine; phosphorus trichloride In toluene at 0 - 20℃; Product distribution / selectivity;74.35%
ethyl bromoacetate
105-36-2

ethyl bromoacetate

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

1-ethoxycarbonylmethoxynaphthalene-2-carboxylic acid
1009813-72-2

1-ethoxycarbonylmethoxynaphthalene-2-carboxylic acid

Conditions
ConditionsYield
With potassium carbonate; tetrabutylammomium bromide In tetrahydrofuran at 30℃; for 0.166667h;90%
allyl bromide
106-95-6

allyl bromide

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

1-(2-propenoxy)-2-naphthoic acid
1009813-71-1

1-(2-propenoxy)-2-naphthoic acid

Conditions
ConditionsYield
With potassium carbonate; tetrabutylammomium bromide In tetrahydrofuran at 30℃; for 0.166667h;90%
manganese(II) hydroxide

manganese(II) hydroxide

water
7732-18-5

water

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

tetraaquabis(1-hydroxy-2-naphthoato-κO)manganese(II)
869582-71-8

tetraaquabis(1-hydroxy-2-naphthoato-κO)manganese(II)

Conditions
ConditionsYield
In water suspn. of Mn(OH)2 in H2O added to suspn. of acid in water; mixt. heated at 313 K for 6 wk; sepd. by decantation; dried at room temp.;90%
methyl iodide
74-88-4

methyl iodide

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

1-methoxy-2-naphthoic acid
883-21-6

1-methoxy-2-naphthoic acid

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 90℃; for 10h; Cooling with ice;90%
1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

C22H14N2O3

C22H14N2O3

Conditions
ConditionsYield
With Vilsmeier reagent; hydrazine hydrate; triethylamine In acetonitrile at 20℃; for 8h;90%
4-methyl-1,2-diaminobenzene
496-72-0

4-methyl-1,2-diaminobenzene

1-hydroxy-2-naphthoic acid
86-48-6

1-hydroxy-2-naphthoic acid

2-(5-methyl-1H-benzo[d]imidazol-2-yl)naphthalen-1-ol

2-(5-methyl-1H-benzo[d]imidazol-2-yl)naphthalen-1-ol

Conditions
ConditionsYield
With polyphosphoric acid for 0.166667h; Microwave irradiation;90%

86-48-6Relevant articles and documents

A dual probe for selective sensing of Zn (II) by fluorescent and Cu (II) by colorimetric methods in different systems based on 7,8-benzochromone-3-carbaldehyde -(fluorescein)hydrazone

Li, Si-liang,Li, Tian-rong,Liu, Cong,Liu, Kui,Sun, Jie,Tian, Li-mei,Xue, Jia,Yang, Zheng-yin

, (2021)

In this study, a novel fluorescent probe sensor, 7,8-benzochromone-3-carbaldehyde (fluorescein)hydrazone L, was designed and synthesized. Based on the photoinduced electron transfer (PET) process, L can detect Zn2+ in the solution of EtOH/H2O (9/1, V/V). The probe had high selectivity and sensitivity to Zn2+ with a lower detection limit of 3.4 × 10?7 M. Furthermore, the coordination ratio of L-Zn2+ was 1:1, which could be corroborated by Job's plot. In addition, in the EtOH/ H2O (5/2, V/V) solution of the probe L, Cu2+ was added to produce a marked change in color from achromatous to yellow, indicating that the probe L could detect Cu2+ by colorimetry, which was detectable by the naked eye, simply and quickly. According to the Benesi-Hildebrand equation, the complexing constants values of L-Zn2+ and L-Cu2+ were 9.8 × 104 M-1 and 1.009 × 105 M-1, respectively.

Negative correlations between cultivable and active-yet-uncultivable pyrene degraders explain the postponed bioaugmentation

Jiang, Bo,Chen, Yating,Xing, Yi,Lian, Luning,Shen, Yaoxin,Zhang, Baogang,Zhang, Han,Sun, Guangdong,Li, Junyi,Wang, Xinzi,Zhang, Dayi

, (2021/09/24)

Bioaugmentation is an effective approach to remediate soils contaminated by polycyclic aromatic hydrocarbons (PAHs), but suffers from unsatisfactory performance in engineering practices, which is hypothetically explained by the complicated interactions between indigenous microbes and introduced degraders. This study isolated a cultivable pyrene degrader (Sphingomonas sp. YT1005) and an active pyrene degrading consortium (Gp16, Streptomyces, Pseudonocardia, Panacagrimonas, Methylotenera and Nitrospira) by magnetic-nanoparticle mediated isolation (MMI) from soils. Pyrene biodegradation was postponed in bioaugmentation with Sphingomonas sp. YT1005, whilst increased by 30.17% by the active pyrene degrading consortium. Pyrene dioxygenase encoding genes (nidA, nidA3 and PAH-RHDα-GP) were enriched in MMI isolates and positively correlated with pyrene degradation efficiency. Pyrene degradation by Sphingomonas sp. YT1005 only followed the phthalate pathway, whereas both phthalate and salicylate pathways were observed in the active pyrene degrading consortium. The results indicated that the uncultivable pyrene degraders were suitable for bioaugmentation, rather than cultivable Sphingomonas sp. YT1005. The negative correlations between Sphingomonas sp. YT1005 and the active-yet-uncultivable pyrene degraders were the underlying mechanisms of bioaugmentation postpone in engineering practices.

General method for the synthesis of salicylic acids from phenols through palladium-catalyzed silanol-directed C-H carboxylation

Wang, Yang,Gevorgyan, Vladimir

, p. 2255 - 2259 (2015/02/19)

A silanol-directed, palladium-catalyzed C-H carboxylation reaction of phenols to give salicylic acids has been developed. This method features high efficiency and selectivity, and excellent functional-group tolerance. The generality of this method was demonstrated by the carboxylation of estrone and by the synthesis of an unsymmetrically o,o′-disubstituted phenolic compound through two sequential C-H functionalization processes.

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