Most professional and biggest manufacturer of 9-Phenylacridine 9-PA 602-56-2 1. Name: 9-Phenylacridine 9-PA 2. Molecular Formula: C19H13N 3. Molecular Weight: 255.31 4. Melting Point: 184°C 5. Packing: 25kg/drum 6. CAS No.: 602-56-2 9-Phe
Cas:602-56-2
Min.Order:50 Kilogram
FOB Price: $100.0
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Cas:602-56-2
Min.Order:100 Gram
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inquiryDayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:602-56-2
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryProduct description: Product name 9-Phenylacridine CAS number 602-56-2 Assay ≥98% Appearance Yellow crystal Capacity 200mt/year Application Photoinitiator, electroplating, Dy
Cas:602-56-2
Min.Order:10 Gram
FOB Price: $12.0
Type:Lab/Research institutions
inquiryThe company has a professional R & D team, mature technology, very competitive prices and stable high quality products for customers to order high quality and low price product efforts! Appearance:Yellow crystalline powder Storage:Sealed, dry,
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
High purity with stable quality. Appearance:Yellow crystal Application:organic synthesis, pharmacy intermediates
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Cas:602-56-2
Min.Order:5 Kiloliter
FOB Price: $1.2 / 5.0
Type:Manufacturers
inquiry9-Phenylacridine Basic information Product Name: 9-Phenylacridine Synonyms: 9-phenyl-acridin;phenylacridine;9-PHENYLACRIDINE;Acridine, 9-phenyl- CAS: 602-56-2
Cas:602-56-2
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
Cas:602-56-2
Min.Order:1 Kilogram
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inquiryName 9-Phenylacridine Other name 9-Phenylacridin;Acridine, 9-phenyl-;3-propan-2-yloxy-1-cyclohex-2-enone CAS 602-56-2
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Cas:602-56-2
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryProduct Name: 9-Phenylacridine CAS: 602-56-2 MF: C19H13N MW: 255.31 EINECS: 210-020-3 Mol File: 602-56-2.mol 9-Phenylacridine Structure 9-Phenylacridine Chemical Properties Melting point 184°C Boiling point 388.54°
9-Phenylacridine CAS:602-56-2 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic intermedia
Cas:602-56-2
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Min.Order:0 Metric Ton
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inquiryA substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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Min.Order:4 Kilogram
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Type:Lab/Research institutions
inquiryJ&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
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
Cas:602-56-2
Min.Order:10 Gram
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Type:Lab/Research institutions
inquiryHunan chemfish Pharmaceutical co.,Ltd.located in Lugu High-tech industral park ,Hunan province . with its own R&D center and more than 10000㎡manufacture plant . Chemfish owns 40 reactors from 1000L to 8000L. With complete auxiliary equipment as
Product name: 9-Phenylacridine CAS No.:602-56-2 Molecule Formula:C19H13N Molecule Weight:255.31 Purity: 99.0% Package: 25kg/drum Description:Yellow powder Manufacture Standards:Enterprise Standard TESTING ITEMS
Cas:602-56-2
Min.Order:1 Kilogram
Negotiable
Type:Trading Company
inquiryOur Advantages A. International Top level TechnologyOur company owned biomedicine experts are famous at home and abroad with rich experience in research and development in the field of efficient chiral functional molecules research and development an
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factory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
Cas:602-56-2
Min.Order:1 Kilogram
FOB Price: $18.0 / 20.0
Type:Trading Company
inquiryShandong Mopai Biotechnology 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 chemicals. W
1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
High quality,stable supply chain.Appearance:white/off-white or light yellow Storage:Store in cool and dry place, keep away from strong light and heat. Package:aluminum bottle,glass bottle,PTFE bottle,cardboard drum Application:This product can be use
GOLDEN PHARMA CO.,LIMITED.is a professional pharmaceutical company,our team have more than 20years expereince in pharmaceutical production and sales. we are a professional technical enterprise specializing in the R & D, production,QA regulation
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Cas:602-56-2
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inquiry9-phenylacridine
Conditions | Yield |
---|---|
With copper(I) oxide; hypophosphorous acid In dichloromethane; water; acetonitrile at 0 - 20℃; | 100% |
Conditions | Yield |
---|---|
With potassium phosphate In toluene at 100℃; for 24h; Catalytic behavior; Reagent/catalyst; Solvent; Time; Temperature; Suzuki-Miyaura Coupling; Schlenk technique; Inert atmosphere; | 99% |
With tetrakis(triphenylphosphine) palladium(0); sodium carbonate In water; toluene at 40℃; for 3h; | 96.8% |
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In 1,2-dimethoxyethane; ethanol; water at 90℃; for 24h; Inert atmosphere; | 87% |
With palladium(II) acetate bis(diphenylphosphino)ferrocene; sodium carbonate In N,N-dimethyl-formamide at 100 - 110℃; for 16h; Phenylation; | 60% |
With potassium phosphate; palladium diacetate; tricyclohexylphosphine In water; toluene Reflux; |
phenyl(2-(phenylamino)phenyl)methanone
9-phenylacridine
Conditions | Yield |
---|---|
With t-butyl bromide In 2,2,2-trifluoroethanol at 20℃; for 24h; Solvent; Inert atmosphere; | 95% |
With hydrogen iodide; iodine In methanol for 12h; Irradiation; | 63% |
With hydrogen iodide; iodine In methanol at 32℃; for 12h; Irradiation; | 63% |
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; methanesulfonic acid; palladium diacetate In water at 100℃; for 24h; | 94% |
With [2,2]bipyridinyl; methanesulfonic acid; palladium diacetate In water at 100℃; for 24h; Catalytic behavior; Reagent/catalyst; Solvent; Temperature; Schlenk technique; | 93% |
Conditions | Yield |
---|---|
Stage #1: (2-aminophenyl)(phenyl)methanone; phenylboronic acid With copper diacetate In 2,2,2-trifluoroethanol at 20℃; for 12h; Stage #2: With t-butyl bromide In 2,2,2-trifluoroethanol at 20℃; for 24h; Reagent/catalyst; Solvent; | 91% |
With copper(II) bis(trifluoromethanesulfonate) In 1,1,2,2-tetrachloroethane at 100℃; for 14h; Reagent/catalyst; Solvent; Temperature; Sealed tube; | 90% |
9-phenyl-9,10-dihydroacridine
9-phenylacridine
Conditions | Yield |
---|---|
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In benzene Heating; | 90% |
With diphenylzinc In toluene at 130℃; for 20h; | 78% |
With potassium hydroxide; potassium hexacyanoferrate(III); benzene |
Conditions | Yield |
---|---|
Stage #1: (2-aminophenyl)(phenyl)methanone; potassium phenyltrifluoborate With copper diacetate In 2,2,2-trifluoroethanol at 20℃; for 12h; Stage #2: With t-butyl bromide In 2,2,2-trifluoroethanol at 20℃; for 24h; | 86% |
Conditions | Yield |
---|---|
With 2-aminopyridine; palladium(II) trimethylacetate; oxygen; citric acid In toluene at 110℃; under 760.051 Torr; for 18h; Catalytic behavior; Reagent/catalyst; Solvent; Temperature; | 83% |
With oxygen; tris-(o-tolyl)phosphine; palladium dichloride In toluene; 1,1,2,2-tetrachloroethane at 160℃; for 24h; Catalytic behavior; Reagent/catalyst; Solvent; Temperature; Sealed tube; | 82% |
9-phenyl-1,2,3,4-tetrahydroacridine
9-phenylacridine
Conditions | Yield |
---|---|
With 2-aminopyridine; palladium(II) trimethylacetate; oxygen In toluene at 110℃; under 760.051 Torr; for 18h; Reagent/catalyst; regioselective reaction; | 82% |
With 1,10-Phenanthroline; palladium(II) trifluoroacetate; oxygen In 1-methyl-pyrrolidin-2-one at 100℃; for 6h; | 75% |
Conditions | Yield |
---|---|
With chloro(1,5-cyclooctadiene)rhodium(I) dimer; tricyclohexylphosphine In toluene at 160℃; for 20h; Inert atmosphere; regioselective reaction; | 81% |
Diphenyliodonium triflate
(2-aminophenyl)(phenyl)methanone
9-phenylacridine
Conditions | Yield |
---|---|
With copper(l) iodide In 1,2-dichloro-ethane at 65℃; for 12h; Friedel-Crafts Alkylation; Inert atmosphere; Sealed tube; | 76% |
Conditions | Yield |
---|---|
Stage #1: (2-aminophenyl)diphenylmethanol; chloroacetonitrile With perchloric acid In nitromethane for 1h; Reflux; Stage #2: With sodium hydroxide In water for 0.166667h; Reflux; | 75% |
2-(trimethylsilyl)phenyl trifluoromethanesulfonate
(2-aminophenyl)(phenyl)methanone
9-phenylacridine
Conditions | Yield |
---|---|
With tetrabutylammonium triphenyldifluorosilicate In 1,2-dimethoxyethane at 20℃; for 24h; Sealed vial; | 72% |
Conditions | Yield |
---|---|
With oxygen; copper diacetate In 1,3,5-trimethyl-benzene at 170℃; under 760.051 Torr; for 6h; Reagent/catalyst; Temperature; | 72% |
Conditions | Yield |
---|---|
With oxygen; tris-(o-tolyl)phosphine; palladium dichloride In toluene; 1,1,2,2-tetrachloroethane at 160℃; for 24h; Sealed tube; | 66% |
Conditions | Yield |
---|---|
With phthalic acid dimethyl ester; zinc(II) chloride at 100℃; for 2h; Microwave irradiation; | 65% |
With zinc(II) chloride at 200 - 210℃; for 0.0833333h; microwave irradiation; | 37% |
With zinc(II) chloride at 260℃; |
Triphenylmethylamin
A
9-phenylacridine
B
2-methyl-4,4-diphenyl-4H-benzo[d][1,3]oxazine
Conditions | Yield |
---|---|
With copper diacetate In 1,3,5-trimethyl-benzene at 170℃; under 760.051 Torr; for 8h; Reagent/catalyst; Temperature; | A 62% B 1 %Chromat. |
N,N-diphenylbenzamide
A
9-phenylacridine
B
4-benzoyldiphenylamine
C
9H-carbazole
Conditions | Yield |
---|---|
With iodine In methanol at 32℃; for 35h; Irradiation; | A 22% B 59% C 8% |
With iodine In methanol at 32℃; for 35h; Irradiation; | A 22% B 59% C 8% |
With iodine In methanol at 32℃; for 35h; Product distribution; Irradiation; several N-aroyldiphenylamine; | A 22% B 59% C 8% |
Conditions | Yield |
---|---|
With oxygen; tris-(o-tolyl)phosphine; palladium dichloride In toluene; 1,1,2,2-tetrachloroethane at 160℃; for 36h; Sealed tube; | 55% |
9-phenylacridine
Conditions | Yield |
---|---|
Stage #1: 10-phenyl-10H-dibenzo[b,e]iodinin-5-ium trifluoromethanesulfonate With sodium azide; triphenylphosphine In N,N-dimethyl acetamide; water at 120℃; for 0.5h; Inert atmosphere; Schlenk technique; Stage #2: With copper(I) thiophene-2-carboxylate; caesium carbonate In N,N-dimethyl acetamide; water at 120℃; for 48h; Inert atmosphere; Schlenk technique; | 53% |
Stage #1: 10-phenyl-10H-dibenzo[b,e]iodinin-5-ium trifluoromethanesulfonate With sodium azide; water; triphenylphosphine In N,N-dimethyl acetamide at 120℃; for 0.5h; Inert atmosphere; Schlenk technique; Stage #2: With copper(I) thiophene-2-carboxylate; caesium carbonate In N,N-dimethyl acetamide at 120℃; for 48h; Inert atmosphere; Schlenk technique; | 53% |
2-phenyl-4,4,5,5-tetramethyl-1,3,2-dioxoborole
(2-aminophenyl)(phenyl)methanone
9-phenylacridine
Conditions | Yield |
---|---|
Stage #1: 2-phenyl-4,4,5,5-tetramethyl-1,3,2-dioxoborole; (2-aminophenyl)(phenyl)methanone With copper diacetate In 2,2,2-trifluoroethanol at 20℃; for 12h; Stage #2: With t-butyl bromide In 2,2,2-trifluoroethanol at 20℃; for 24h; | 52% |
Conditions | Yield |
---|---|
With palladium(II) acetate bis(diphenylphosphino)ferrocene; sodium carbonate In N,N-dimethyl-formamide at 100 - 110℃; for 16h; Phenylation; | 50% |
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In 1,4-dioxane; water at 100℃; for 8h; Suzuki Coupling; Inert atmosphere; |
Conditions | Yield |
---|---|
With palladium(II) acetate bis(diphenylphosphino)ferrocene; sodium carbonate In N,N-dimethyl-formamide at 100 - 110℃; for 16h; Phenylation; | 38% |
phenyllithium
2-(trifluoromethyl)benzenamine
A
9-phenylacridine
B
o-Aminophenyl-triphenylmethan
Conditions | Yield |
---|---|
In tetrahydrofuran -78 deg C, 30 min -> 0 deg C; | A 31% B 25% |
Conditions | Yield |
---|---|
With palladium(II) acetate bis(diphenylphosphino)ferrocene; sodium carbonate In N,N-dimethyl-formamide at 100 - 110℃; for 16h; Phenylation; | 30% |
[1-Phenyl-1-(2-phenylamino-phenyl)-meth-(E)-ylideneaminooxy]-ethaneperoxoic acid tert-butyl ester
A
9-phenylacridine
Conditions | Yield |
---|---|
In various solvent(s) for 1h; Heating; | A 20% B 8% C 27% |
Conditions | Yield |
---|---|
With palladium(II) acetate bis(diphenylphosphino)ferrocene; sodium carbonate In N,N-dimethyl-formamide at 100 - 110℃; for 16h; Phenylation; | 23% |
Conditions | Yield |
---|---|
In various solvent(s) for 1h; Heating; | A 18% B 2% C 7% D 17% |
[1-(2-Diphenylamino-phenyl)-1-phenyl-meth-(E)-ylideneaminooxy]-ethaneperoxoic acid tert-butyl ester
A
9-phenylacridine
B
9,10-diphenyl-9,10-dihydro-acridine
Conditions | Yield |
---|---|
In various solvent(s) for 1h; Heating; | A 5% B 16% C 7% D 15% |
In various solvent(s) for 1h; Heating; | A 5% B 16% C 7% D 7% |
Conditions | Yield |
---|---|
for 10h; Sealed tube; | 99.6% |
In acetonitrile at 85℃; for 24h; Sealed tube; | 76% |
for 3h; Reflux; Inert atmosphere; | 75% |
9-phenylacridine
methyl trifluoromethanesulfonate
10-methyl-9-phenylacridinium trifluoromethanesulphonate
Conditions | Yield |
---|---|
In dichloromethane | 82% |
With 2,6-di-tert-butyl-pyridine In dichloromethane at 20℃; for 3h; | 79% |
With 2,6-di-tert-butyl-pyridine In dichloromethane at 20℃; for 3h; | 79% |
9-phenylacridine
1,2-dichloro-ethane
9,10-ethano-9,10-dihydro-9-phenylacridine
Conditions | Yield |
---|---|
With sodium In tetrahydrofuran the reductive metalation of the compound and the reactions of the dianion with electrophiles; | 71% |
With sodium 1.)THF, 5 h 2.)-70 deg C to 20 deg C; Yield given. Multistep reaction; |
9-phenylacridine
9-phenyl-9,10-dihydroacridine
Conditions | Yield |
---|---|
With hydrogen In toluene at 120℃; under 22502.3 Torr; for 48h; Autoclave; | 70% |
With hydrogenchloride; zinc | |
With sodium amalgam; ethanol |
Conditions | Yield |
---|---|
With bis(1,5-cyclooctadiene)nickel (0); N,N′-bis(2,6-diisopropylphenyl)imidazolylidene hydrochloride; sodium t-butanolate In toluene at 160℃; for 20h; Inert atmosphere; regioselective reaction; | 68% |
9-phenylacridine
dimethyl sulfate
9-methyl-9-phenyl-10-methyl-9,10-dihydroacridine
Conditions | Yield |
---|---|
With sodium In tetrahydrofuran the reductive metalation of the compound and the reactions of the dianion with electrophiles; | 61% |
With sodium 1.)THF, 5 h 2.)-70 deg C to 20 deg C; Yield given. Multistep reaction; |
9-phenylacridine
A
9-phenyl-1,2,3,4-tetrahydroacridine
B
9-phenyl-1,2,3,4,5,6,7,8-octahydro-acridine
C
9-phenyl-9,10-dihydroacridine
Conditions | Yield |
---|---|
With hydrogenchloride; nickel-aluminium In 1,4-dioxane at 95℃; | A 14% B 58% C 14% |
9-phenylacridine
bis(2-methylphenyl)zinc
9-phenyl-4-(2-tolyl)acridine
Conditions | Yield |
---|---|
With bis(1,5-cyclooctadiene)nickel (0); N,N′-bis(2,6-diisopropylphenyl)imidazolylidene hydrochloride; sodium t-butanolate In toluene at 160℃; for 20h; Inert atmosphere; regioselective reaction; | 52% |
9-phenylacridine
Conditions | Yield |
---|---|
With N-Bromosuccinimide In acetonitrile at 65℃; for 12h; Inert atmosphere; | 52% |
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