CAS No.95-55-6,2-Aminophenol Suppliers

Jiangsu Huaen Energy Co., Ltd.

White or light gray crystalline powder

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Simagchem Corporation

Welcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our

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Jinan Finer Chemical Co., Ltd

Product Description Product Name 2-Aminophenol CAS No. 95-55-6 Appearance White crystalline powder Assay ≥99% Capacity 500mt/year Min.packing 100gram

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Henan Allgreen Chemical Co.,Ltd

good quality Appearance:Solid Storage:Keep in a cool dry place Package:meet the customer's demand Application:dye intermediate Transportation:by sea or by air Port:shanghai

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EAST CHEMSOURCES LIMITED

2-Aminophenol Appearance: white needle-like crystal Melting point: 172～177°C Boiling point: 164°C (11 mmHg) Flash point: 168°C Relativ

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Ality Chemical Corporation

The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi

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Dayang Chem (Hangzhou) Co.,Ltd.

As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem’s R&D center offer custom synthesis according to the contract research and development services for t

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Chemwill Asia Co., Ltd.

CHemwill -- 2-Aminophenol

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Henan Tianfu Chemical Co., Ltd.

Competitive Price High Quality Fast Delivery custom-made Welcome to Henan Tianfu Chemical Co., Ltd. website. Our company engages in Sodium Tripolyphosphate (STPP) and Sodium Hexametabphosphate (SHMP) production; development of noble me

95-55-6,2-Aminophenol

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Henan Sinotech Import&Export Corporation

Chemical Name 2-Aminophenol Synonyms 2-Amino-1-hydroxybenzene ; o-Hydroxyaniline Molecular Formula C6H7NO

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Henan Wentao Chemical Product Co., Ltd.

Henan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod

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Hangzhou Keyingchem Co.,Ltd

Hangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det

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Hangzhou J&H Chemical Co., Ltd.

J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia

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Zibo Hangyu Biotechnology Development Co., Ltd

Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi

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HANGZHOU YUNUO CHEMICAL CO.,LTD

Superior quality, moderate price & quick delivery. Appearance:offwhite crystalline powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum, or as per your request. Application:For medicine , pesti

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Siwei Development Group Ltd.

Product name: O-Aminophenol CAS No.：95-55-6 Molecule Formula：C6H7NO Molecule Weight：109.13 Purity: 99.0% Package: 25kg/drum Description：White or gray crystalline powder Manufacture Standards：Enterprise Standard TES

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Hunan chemfish Pharmaceutical co.,Ltd

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SAGECHEM LIMITED

SAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in

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Kono Chem Co.,Ltd

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GIHI CHEMICALS CO.,LIMITED

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JINHUA HUAYI CHEMICAL CO., LTD.

Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands

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Hangzhou Dingyan Chem Co., Ltd

high purity, manufacturer Application:Intermediate

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Wuhan Fortuna Chemical Co.,Ltd

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Aecochem Corp.

Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS

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Wuhan Rison Trading., Co., Ltd

2-Aminophenol CASNo:95-55-6 Molecular Formula: C6H7NO M.P.: 174℃ B.P.: 153℃(1.47kPa) Relative Density: 1.328Appearance:white needle-like crystal Storage:Store in a cool, dry place. Keep container closed when not in use. Package:25kg/drum or at the r

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Zhuozhou Wenxi import and Export Co., Ltd

Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard

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Antimex Chemical Limied

Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali

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Xiamen AmoyChem Co.,Ltd

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Hubei Langyou International Trading Co., Ltd

sell high purity of 2-Aminophenol Application:sell high purity of 2-Aminophenol

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Luyunjia Chemistry Xiamen Limited

Xiamen Luyunjia Trading Co.,Ltd Package:1kg/bag; 620kg/drum, or as customer's request. Application:Xiamen Luyunjia Trading Co.,Ltd Transportation:DHL, EMS, FedEx, TNT, AIR, SEA Port:Beijing，Shanghai，Guangzhou ,China main port

2-AMINOPHENOL

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Synthetic route

: 88-75-5
2-hydroxynitrobenzene

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With hydrogen; Pd in AV-17-8-Pd In ethanol at 40℃;	100%
With hydrogen; Pd in AV-17-8-Pd In ethanol at 40℃; under 760 Torr; Rate constant;	100%
With hydrogen; palladium-containing anion exchanger AB-17-8-Pd In ethanol at 20 - 40℃; under 750.06 Torr; Kinetics; Product distribution; Further Variations:; Catalysts;	100%

: 59-49-4
2-Benzoxazolinone

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With ammonium bromide; ethylenediamine at 70℃; for 2h; Microwave irradiation;	99%
In 1,2-dichloro-ethane at 95 - 105℃; under 0 - 1125.11 Torr; Alkaline conditions; Large scale;	96.5%
With sodium hydroxide In water at 100℃; for 16h;	72%
Alkaline hydrolysis;

: 533-58-4
2-Iodophenol

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With [Cu2(2,7-bis(pyridin-2-yl)-l,8-naphthyridine)(OH)(CF3COO)3]; tetrabutylammomium bromide; ammonia; caesium carbonate In water at 110 - 120℃; for 16h; Sealed tube;	99%
With ammonium hydroxide In water at 20℃; for 9h; Green chemistry;	96%

: 5570-18-3
2-aminophenylboronic acid

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With dihydrogen peroxide In neat (no solvent) at 30℃; for 0.3h; Green chemistry;	90%
With water; oxygen; sodium sulfite at 50℃; for 2h; Green chemistry;	72%

: 36309-44-1
2-((trimethylsilyl)oxy)aniline

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With methanol; 1,3-disulfonic acid imidazolium hydrogen sulfate at 20℃; for 0.0833333h; Green chemistry;	98%
With rice husk ash supported on anatase-phase titania nanoparticles nanocomposite In methanol at 20℃; for 0.05h;	94%
With nano magnetic sulfated zirconia (Fe3O4 at ZrO2/SO42-) In neat (no solvent) at 20℃; for 0.333333h; Green chemistry;	90%

: 95-56-7
2-hydroxybromobenzene

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With ammonium hydroxide In water at 20℃; for 9h; Green chemistry;	93%
With ammonium hydroxide; L-2-O-methyl-chiro-inositol; copper(II) acetate monohydrate; potassium iodide In 1-methyl-pyrrolidin-2-one at 150℃; for 12h;	70%
With ammonium hydroxide; copper at 80℃; for 7h; Inert atmosphere;	65.5%

: 108-95-2
phenol

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
Stage #1: phenol With copper(ll) sulfate pentahydrate; copper In water at 30℃; for 2h; Inert atmosphere; Sealed tube; Stage #2: With ammonium hydroxide; sodium hydroxide In water at 20℃; for 1h; pH=~ 9; Inert atmosphere; Sealed tube;
Multi-step reaction with 2 steps 1: nitric acid; sulfuric acid / water / 2 h / 50 - 55 °C 2: iron; acetic acid / water / 0.75 h / Reflux View Scheme
Multi-step reaction with 2 steps 1: nitric acid; sulfuric acid / 1.08 h / 15 - 25 °C / 9000.9 Torr 2: hydrogenchloride; zinc / water / 1.5 h / 70 °C / 9750.98 Torr / Sealed tube View Scheme
Multi-step reaction with 2 steps 1.1: acetic acid 1.2: 12 h / 0 - 25 °C 2.1: ammonium hydroxide; copper / 7 h / 80 °C / Inert atmosphere View Scheme

: 2050-14-8
2,2'-Dihydroxyazobenzene

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With aminomethyl polysterene resin formic acid salt; zinc In methanol at 20℃; for 0.3h;	96%
With polystyrene-CH2-NH3(+)HCO2(-); magnesium In methanol at 20℃; for 0.266667h;	96%
With aminomethylpolystyrene-supported formate; palladium on activated charcoal In methanol at 20℃; for 3.5h;	95%

: 273-53-0
benzoxazole

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With trifluoroacetic acid In isopropyl alcohol at 70℃; for 18h;	67%
With bis(triphenylphosphine)copper(I) cyanide; caesium carbonate; triphenylphosphine Reagent/catalyst;	62%
With ethylene glycol; zinc(II) chloride In neat (no solvent) at 120℃; for 6h; Green chemistry;	62%

: 2382-96-9
benzo[d]oxazole-2-(3H)-thione

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With 3-azapentane-1,5-diamine at 130℃; for 2h; Sealed tube;	98%
With ammonium bromide; ethylenediamine at 80℃; for 5h; Microwave irradiation;	91%

: 24541-44-4
2-azidophenol

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With hydrazinium monoformate; zinc In methanol at 20℃; for 0.166667h;	96%
With zinc In methanol at 20℃; for 4h;	96%
With aluminium(III) iodide In benzene for 0.25h; Reduction; Heating;	95%
With ammonium formate; zinc In methanol at 20℃; for 0.3h;	85%

: 615-43-0
2-iodophenylamine

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
Stage #1: 2-iodophenylamine With copper(l) iodide; 8-Hydroxyquinoline-N-oxide In dimethyl sulfoxide at 20℃; for 0.166667h; Inert atmosphere; Stage #2: With cesiumhydroxide monohydrate In water; dimethyl sulfoxide at 100℃; for 36h; Inert atmosphere;	84%
With copper(l) iodide; lithium pipecolinate; tetrabutyl ammonium fluoride; sodium hydroxide In water at 130℃; for 24h;	74%

: 90-04-0
2-methoxy-phenylamine

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With 1-methyl-pyrrolidin-2-one; potassium carbonate at 190℃; for 0.5h;	80%
With 1-methyl-pyrrolidin-2-one; potassium carbonate; thiophenol for 0.5h; Heating;	80%
With water; hydrogen bromide; Aliquat 336 at 105℃; for 6.5h; Catalytic behavior;	72%
With aluminium trichloride In various solvent(s) for 0.5h; Heating;
With aluminium trichloride

: 88-75-5
2-hydroxynitrobenzene

A: 3009-34-5
quinoneimine

B: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With potassium fluoride; polymethylhydrosiloxane; palladium diacetate In tetrahydrofuran at 20℃; for 0.5h;	A 4% B 94%

: 273-53-0
benzoxazole

: 103-67-3
benzyl-methyl-amine

A: N-benzyl-N-methylbenzo[d]oxazol-2-amine

B: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With dipotassium peroxodisulfate; acetic acid; triphenylphosphine; copper(ll) bromide In water at 40℃; for 6h;	A 15% B n/a

...Expand

: 95-57-8
2-monochlorophenol

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With ammonium hydroxide; potassium phosphate; Cu0.18Bi0.88O0.88I1.06 In ethanol; water at 80℃; for 20h; Inert atmosphere; Green chemistry;	76 %Chromat.

: 88-75-5
2-hydroxynitrobenzene

: 100-51-6
benzyl alcohol

A: 95-55-6
2-amino-phenol

B: 65-85-0
benzoic acid

Conditions

Conditions	Yield
With potassium hydroxide In 1,3,5-trimethyl-benzene at 160℃; for 24h; Inert atmosphere; Overall yield = 85 percent;

...Expand

1-azido-2-(Wang resin-CH2O)-benzene: 1-azido-2-(Wang resin-CH2O)-benzene

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate; ethanethiol In dichloromethane at 20℃; for 2h;	90%

: 121555-67-7
2,6-Dichloro-3,5-difluoro-4-nitro-phenol

A: 2,6-Dichloro-3,5-difluoro-4-amino-phenol

B: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With hydrogen In methanol; aluminum nickel
With hydrogen In methanol; aluminum nickel
With hydrogen In methanol; aluminum nickel

: 62-53-3
aniline

A: 123-30-8
4-amino-phenol

B: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With hydrogenchloride; sodium acetate; hemin; rac-cysteine In water; acetone at 40℃; for 2h; Mechanism; pH=3; pH and reaction time dependency, various catalysts and inhibitors;
With dihydrogen peroxide; FePp In ethanol at 38℃; for 0.166667h; Product distribution; borate buffer, pH 9; further educts;
With oxygen; titanium(IV) oxide In water at 26.84℃; for 1.5h; pH=6.5; Irradiation; Title compound not separated from byproducts.;
With dihydrogen peroxide; bis(triphenyl)oxodiphosphonium trifluoromethanesulfonate salt In ethanol; water at 20℃; for 0.666667h; Overall yield = 80 %; Overall yield = 0.087 g;

: 69589-21-5
2-((tert-butyldimethylsilyl)oxy)aniline

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With tin(ll) chloride In ethanol at 20℃; for 5h;	88%

: 116296-18-5
(E)-2-(phenyldiazenyl)phenyl benzoate

A: 93-98-1
N-phenyl benzoyl amide

B: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With ammonium chloride; zinc In methanol at 80℃; for 6h; Inert atmosphere;	A 71% B 64%

: 91-23-6
2-Nitroanisole

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With 1,3-dimethyl-2-imidazolidinone; sodium trimethylsilanethiolate at 185℃; for 24h;	96%

: 121555-68-8
2-chloro-3,5,6-trifluoro-4-nitrophenol

A: 2-Chloro-3,5,6-trifluoro-4-amino-phenol

B: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
aluminum nickel In methanol

: 107-21-1
ethylene glycol

: 108-95-2
phenol

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With hydrogenchloride; paraformaldehyde In water

: 127-17-3
2-oxo-propionic acid

: 88-75-5
2-hydroxynitrobenzene

A: 84529-13-5
3-methyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one

B: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With palladium 10% on activated carbon; hydrogen In water; isopropyl alcohol at 30℃; under 7500.75 Torr; for 10h; Autoclave;	A 28% B n/a

...Expand

: 89466-08-0
2-hydroxyphenyl boronic acid

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With sodium hydroxide; hydroxylamine-O-sulfonic acid In acetonitrile at 20℃; for 16h;	80%

: (E)-1-(2-hydroxyphenyl)-3-(3-(thiophen-2-yl)acryloyl)thiourea

A: 1124-65-8, 15690-25-2, 51019-83-1
3-(2-thienyl)-2-propenoic acid

B: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With sodium hydroxide In ethanol for 1h; Reflux;

: 2-(pyrimidin-2-ylamino)phenyl 4-chlorobenzoate

: 95-55-6
2-amino-phenol

Conditions

Conditions	Yield
With hydrogenchloride In water at 150℃; for 3h; Microwave irradiation; Sealed tube;	71%

: 614-80-2
2-(acetylamino)phenol

A: 95-55-6
2-amino-phenol

B: 614-70-0
2-ethylaminophenol

Conditions

Conditions	Yield
With [bis(2-methylallyl)cycloocta-1,5-diene]ruthenium(II); formic acid; bis(trifluoromethanesulfonyl)amide; triethylamine; [2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine] In dibutyl ether at 130℃; for 24h;	A 83% B n/a

: 100-52-7
benzaldehyde

: 95-55-6
2-amino-phenol

: 833-50-1
2-phenylbenzo[d]oxazole

Conditions

Conditions	Yield
With Au NCs/TiO2 In toluene at 130℃; Inert atmosphere;	100%
With ISO-PECH polyamine catalyst In methanol at 20℃; for 0.0666667h; Green chemistry;	99%
With Co-doped NiFe2O4 nanoparticle In neat (no solvent) at 70℃; for 2h;	97%

: 95-55-6
2-amino-phenol

: 762-42-5
dimethyl acetylenedicarboxylate

: 66628-73-7
(2Z)-[2-oxo-2H-1,4-benzoxazine-3(4H)-ylidene]acetic acid methyl ester

Conditions

Conditions	Yield
at 20℃; for 0.0666667h; Michael addition;	100%
In neat (no solvent) at 20℃; for 0.166667h; regioselective reaction;	98%
In ethanol at 0℃; for 3h;	94%

: 100-52-7
benzaldehyde

: 95-55-6
2-amino-phenol

: 3230-45-3
(E)-N-benzylidene-2-hydroxyaniline

Conditions

Conditions	Yield
With magnesium sulfate In tetrahydrofuran at 0 - 20℃; for 8h;	100%
In ethanol at 25℃; for 24h;	91%
In ethanol for 2h; Reflux;	85%

: 120-14-9
3,4-dimethoxy-benzaldehyde

: 95-55-6
2-amino-phenol

: 80241-83-4
2-(3,4-dimethoxyphenylmethyleneimino)phenol

Conditions

Conditions	Yield
In toluene Heating;	100%
In ethanol for 3h; Reflux;	75%

: 75-77-4
chloro-trimethyl-silane

: 95-55-6
2-amino-phenol

: 36309-44-1
2-((trimethylsilyl)oxy)aniline

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 27℃; for 24h; Inert atmosphere; Glovebox;	100%
With triethylamine In dichloromethane at 20℃; for 18h;	80.5%
	76%

: 73568-25-9
2-chloro-3-quinoline carboxaldehyde

: 95-55-6
2-amino-phenol

: 112697-88-8
2-((2-chloroquinolin-3-yl)methyleneamino)phenol

Conditions

Conditions	Yield
In tetrahydrofuran for 2h; Ambient temperature;	100%
In ethanol at 20℃; for 0.333333h; Sonication;	78%
With acetic acid In ethanol at 20℃;

: 1066-35-9
dimethylmonochlorosilane

: 95-55-6
2-amino-phenol

: 18245-89-1
2,2-dimethyl-2,3-dihydro-benzo[1,3,2]oxazasilole

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran for 6h; Heating;	100%

: 1118-02-1
trimethylsilyl isocyanate

: 95-55-6
2-amino-phenol

: 75226-86-7
(2-Trimethylsilanyloxy-phenyl)-urea

Conditions

Conditions	Yield
In tetrahydrofuran at 60 - 65℃; for 5h;	100%

: 95-55-6
2-amino-phenol

: 999-97-3
1,1,1,3,3,3-hexamethyl-disilazane

: 36309-44-1
2-((trimethylsilyl)oxy)aniline

Conditions

Conditions	Yield
With 1,3-disulfonic acid imidazolium hydrogen sulfate In neat (no solvent) at 20℃; for 0.0166667h; Green chemistry;	100%
With poly(4-vinylpyridine) In acetonitrile at 20℃; for 0.5h; chemoselective reaction;	98%
With 3-methyl-1-sulfonic acid imidazolium hydrogen sulfate at 20℃; for 0.0833333h; Neat (no solvent); chemoselective reaction;	95%

: 95-55-6
2-amino-phenol

: 2258-42-6
Acetic formic anhydride

: 2843-27-8
N-(2-hydroxyphenyl)formamide

Conditions

Conditions	Yield
In tetrahydrofuran at -20℃; for 0.25h;	100%

: 95-55-6
2-amino-phenol

: 161868-74-2
1,1-dichloro-5-aza-2,8-dioxa-1-phosphaV-dibenzo<9,9',11,11'-tetra-tert-butyl>-bicyclo<3.3.0>octadiene

: C34H45N2O3P

Conditions

Conditions	Yield
In benzene for 24h; Ambient temperature;	100%

: 13154-24-0
triisopropylsilyl chloride

: 95-55-6
2-amino-phenol

: 194869-04-0
2-((triisopropylsilyl)oxy)aniline

Conditions

Conditions	Yield
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 14h; Inert atmosphere;	100%
With 1H-imidazole In dichloromethane at 20℃; for 20h;	99%
With 1H-imidazole In dichloromethane for 33h; Ambient temperature;	84%
With 1H-imidazole; triethylamine In dichloromethane at 20℃; Inert atmosphere;

: 24424-99-5
di-tert-butyl dicarbonate

: 95-55-6
2-amino-phenol

: 186663-74-1
tert-butyl (2-hydroxyphenyl)carbamate

Conditions

Conditions	Yield
copper(II) bis(tetrafluoroborate) at 30 - 33℃; for 1h;	100%
In dichloromethane at 23℃; for 22h; Inert atmosphere;	100%
With Amberlyst-15 In ethanol at 20℃;	100%

: 79099-07-3
N-tert-butyloxycarbonylpiperidin-4-one

: 95-55-6
2-amino-phenol

: 162045-48-9
1-(tert-butoxycarbonyl)-4-[(2-hydroxyphenyl)amino]piperidine

Conditions

Conditions	Yield
	100%
Stage #1: N-tert-butyloxycarbonylpiperidin-4-one; 2-amino-phenol With sodium tris(acetoxy)borohydride In 1,2-dichloro-ethane at 120℃; for 0.0833333h; Microwave irradiation; Stage #2: With water; sodium hydrogencarbonate	75%
With sodium tris(acetoxy)borohydride

: 1122-91-4
4-bromo-benzaldehyde

: 95-55-6
2-amino-phenol

: 117649-27-1, 3230-46-4
2-(4-bromo-benzylidenamino)-phenol

Conditions

Conditions	Yield
In methanol at 20℃; for 1h;	100%
In methanol at 20℃; for 1h;	100%
In ethanol Heating;	96%

: 95-55-6
2-amino-phenol

: 1-bromo-2-[4-(N-piperidinosulfonyl)phenyl]ethanedione 1-phenylhydrazone

: 2-phenylhydrazono-3-[4-(N-piperidinosulfonyl)phenyl]-1,4-benzoxazine

Conditions

Conditions	Yield
With triethylamine In ethanol for 2h; Cyclization; Heating;	100%

: 121-34-6
3-methoxy-4-hydroxybenzoic acid

: 95-55-6
2-amino-phenol

: 3164-07-6
4-(benzo[d]oxazol-2ʹ-yl)-2-methoxyphenol

Conditions

Conditions	Yield
With trimethylsilylphosphate at 180℃; for 0.5h;	100%
With Trimethylsilyl polyphosphate at 180℃; for 16.75h; Cooling with ice;	10.63 g

: 87808-44-4
3-methoxy-4-methylbenzoyl chloride

: 95-55-6
2-amino-phenol

: 669091-09-2
N-(2-hydroxyphenyl)-3-methoxy-4-methylbenzamide

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃;	100%

: 40996-91-6
3-vinyl-cyclohex-2-enone

: 95-55-6
2-amino-phenol

: 906078-77-1
3-[2-(2-aminophenylsulfanyl)ethyl]cyclohex-2-enone

Conditions

Conditions	Yield
With triethylamine In benzene at 0 - 25℃; for 7h;	100%

: 112440-47-8
1,2-bis(2,4,5-trimethylthiophene-3-yl)maleic anhydride

: 95-55-6
2-amino-phenol

: 155876-10-1
N-(2-hydroxyphenyl)-2,3-bis(2,4,5-trimethyl-3-thienyl)maleimide

Conditions

Conditions	Yield
With triethylamine In toluene for 24h; Heating;	100%

: 1121-60-4
pyridine-2-carbaldehyde

: 95-55-6
2-amino-phenol

: (E)-2-((pyridin-2-yl)methyleneamino)phenol

Conditions

Conditions	Yield
acetic acid In ethanol for 12h;	100%
With air In methanol at 60℃; for 1h;	90.9%
In methanol at 20℃;	87%

: 95-55-6
2-amino-phenol

: 4-amino-3-nitrophenylimidic acid ethyl ester hydrochloride

: 132064-15-4
4-(benzo[d]oxazol-2-yl)-2-nitrobenzeneamine

Conditions

Conditions	Yield
In ethanol at 95℃; for 5h;	100%

: 1022157-41-0
ethyl 2-chloro-6-(2-methoxyphenylamino)-5-nitropyrimidine-4-carboxylate

: 95-55-6
2-amino-phenol

: 1022157-68-1
ethyl 2-(2-hydroxyphenylamino)-6-(2-methoxyphenylamino)-5-nitropyrimidine-4-carboxylate

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃;	100%

: C17H21NO4

: 95-55-6
2-amino-phenol

: C23H26N2O4

Conditions

Conditions	Yield
Stage #1: C17H21NO4 With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dimethyl sulfoxide at 20℃; for 18h; Stage #2: 2-amino-phenol In dimethyl sulfoxide; N,N-dimethyl-formamide at 20℃; for 3h;	100%

: 136-77-6
4-Hexylresorcinol

: 95-55-6
2-amino-phenol

: 18102-12-0
5-N-hexyl-2,2',4-trihydroxyazobenzene

Conditions

Conditions	Yield
Stage #1: 2-amino-phenol With hydrogenchloride; sodium nitrite In water at 5℃; for 0.166667h; Stage #2: 4-Hexylresorcinol With sodium hydroxide In water at 5℃; Cooling with ice; Stage #3: With hydrogenchloride In water	100%