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 services. DayangChem can provide different quantities of custom synthesis ch
Cas:206-44-0
Min.Order:1 Kilogram
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Cas:206-44-0
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inquiryThe 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
17-year experience in Phytochemicals Each product has passed very strict tests (NMR\MS\HPLC) Agents in 13 countries Certified by ISO 9001:2008 quality management system Leader Supplier of Botanical Reference Materials in China
Our main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
chengdu and import and export trade co., LTD., who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do res
Fluoranthene Basic information Product Name: Fluoranthene Synonyms: FLUORANTHENE;BENZO(J,K)FLUORENE;1,2-(1,8-naphthalenediyl)benzene;1,2-Benzacenaphthene;1,2-(1,8-N
Cas:206-44-0
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryProduct Name Fluoranthene Synonyms Fluoranthene;Benzo[jk]fluorene CAS: 206-44-0 MF: - MW: - EINECS: - Pr
Cas:206-44-0
Min.Order:5 Metric Ton
FOB Price: $1.0 / 2.0
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inquiryProduct Description Product website: http://www.finerchem.com/pro01en/id/1769.html Product Name Fluoranthene CAS No. 206-44-0
Fluoranthene CAS: 206-44-0 Specification product name fluoranthene cas no. 206-44-0 appearance yellowish to green crystal assay ≥99%,98%,95% capacity 200mt/year min.
Cas:206-44-0
Min.Order:1 Kilogram
FOB Price: $100.0 / 150.0
Type:Other
inquiryHangzhou 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
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
Product name: Fluoranthene CAS No.: 206-44-0 Molecule Formula:C16H10 Molecule Weight:202.25 Purity: 99.0% Package: 25kg/bag Description:Yellow green crystalline powder Manufacture Standards:Enterprise Standard TEST
1.Product name:Fluoranthene 2.CAS:206-44-0 3.MF:C16H10 4.MW:202.2506 5.Appearance:White to yellowish crystlline powder 6.Assay:99%MIN Appearance:white powder Package:as celient requirement Port:ANY PORT OF CHINA
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
high purity,in stock Package:25kg/drum,or as per customers'demand Application:API,or Intermediates,fine chemicals Transportation:air,sea,courier
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
high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Hunan 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 Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:206-44-0
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiryAnsciep 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
Amoychem is committed to providing the top-quality chemical products and services Internationally. We offer our customers with friendly, professional service and reliable, high performance products that have been manufactured according to the accredi
Xiamen Luyunjia Trading Co.,Ltd Package:1kg/bag; 3024kg/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
Chemistry:TOXICITY:SAFETY:Production:Others: Appearance:yellow to green crystalline powder Storage:APPROX 4°C Package:According to your demand Transportation:as requested
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China
Our mission is to provide high-quality and innovative products to our customers. By offering a broad range of products, custom synthesis and personalized services, Bide can help scientists speeding up their research in the chemical and pharmaceutical
we have 3 OEM factories, 2 R&D labs. Aily is striving to improve reseach and development, meet social and customers needs with a unifying strategic idea. Appearance:Colorless or yellow green acicular crystal Storage:Room temperature Package:25k
1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G
fluoranthene
Conditions | Yield |
---|---|
With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; potassium phosphate; tris-(dibenzylideneacetone)dipalladium(0); 1-Adamantanecarboxylic acid In N,N-dimethyl acetamide at 110℃; for 24h; Inert atmosphere; | 98% |
1-(2-fluorophenyl)naphthalene
fluoranthene
Conditions | Yield |
---|---|
With dimethyldimesitylsilane In chlorobenzene at 110℃; for 8h; Friedel Crafts reaction; Inert atmosphere; | 93% |
With aluminum oxide at 150℃; for 60h; Inert atmosphere; | 79% |
1-(2-trifluormethanesulfonyloxyphenyl)naphthalene
fluoranthene
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene; triphenylphosphine; lithium chloride; bis-triphenylphosphine-palladium(II) chloride In N,N-dimethyl-formamide at 140℃; for 6h; | 90% |
With 1,8-diazabicyclo[5.4.0]undec-7-ene; triphenylphosphine; lithium chloride; bis-triphenylphosphine-palladium(II) chloride In N,N-dimethyl-formamide at 140℃; for 6h; other aryl bromides; other MOM phenyl ethers; | 90% |
6b,7,10,10a-tetrahydrofluoranthene-6b,10a-diol
fluoranthene
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene at 75℃; for 6.5h; | 90% |
Conditions | Yield |
---|---|
With tris(dibenzylideneacetone)dipalladium (0); 1,8-diazabicyclo[5.4.0]undec-7-ene; tricyclohexylphosphine In N,N-dimethyl-formamide at 155℃; for 48h; Suzuki coupling, Heck coupling; | 87% |
Conditions | Yield |
---|---|
With tris(dibenzylideneacetone)dipalladium (0); 1,8-diazabicyclo[5.4.0]undec-7-ene; tricyclohexylphosphine In N,N-dimethyl-formamide at 155℃; for 48h; Suzuki coupling, Heck coupling; | 87% |
3,9-Diethynyl-phenanthrene
A
fluoranthene
B
cyclopenta[c,d]pyrene
C
acephenanthrylene
Conditions | Yield |
---|---|
at 1000℃; under 0.01 Torr; Mechanism; var. of temp.; other polyclic aromatic hydrocarbon with ethynyl subst.; | A 2% B 1% C 4% D 8% E 85% |
Conditions | Yield |
---|---|
at 1000℃; under 0.01 Torr; Further byproducts given; | A 2% B 1% C 8% D 85% |
1-phenyl-2-iodonaphthalene
fluoranthene
Conditions | Yield |
---|---|
With palladium diacetate; cesium pivalate; bis-diphenylphosphinomethane In N,N-dimethyl-formamide at 110℃; for 24h; | 81% |
With palladium diacetate; potassium pivalate; DavePhos In N,N-dimethyl-formamide at 100℃; for 24h; Schlenk technique; Inert atmosphere; Sealed tube; | 70% |
With palladium diacetate; cesium pivalate; bis-diphenylphosphinomethane In N,N-dimethyl-formamide at 110℃; for 12h; Inert atmosphere; |
2-(2-bromo-acenaphthylen-yl)-3,6-dihydro-2H-pyran
fluoranthene
Conditions | Yield |
---|---|
With tetrabutyl-ammonium chloride; palladium diacetate; caesium carbonate; triphenylphosphine In N,N-dimethyl-formamide at 85 - 90℃; for 1.5h; Inert atmosphere; | 80% |
Conditions | Yield |
---|---|
at 120℃; for 3h; Sealed tube; | A 11% B 71% |
1-phenyl-2-bromonaphthalene
fluoranthene
Conditions | Yield |
---|---|
With palladium diacetate; cesium pivalate; bis-diphenylphosphinomethane In N,N-dimethyl-formamide at 110℃; for 72h; | 70% |
fluoranthene
Conditions | Yield |
---|---|
Raney Ni (W2) In ethanol for 6h; Heating; | 70% |
(E)-1-(1-buten-3-ynyl)-8-ethynylnaphthalene
fluoranthene
Conditions | Yield |
---|---|
With hydroquinone In xylene at 150℃; for 6h; Cyclization; | 65% |
2-(naphthalen-1-yl)benzenamine
fluoranthene
Conditions | Yield |
---|---|
With tert.-butylnitrite In acetonitrile at 80℃; for 10h; | 65% |
3H-indazole-3-spiro-1'-naphthalen-4'(1'H)-one
fluoranthene
Conditions | Yield |
---|---|
With water; sodium chloride; zinc | 64% |
Multi-step reaction with 3 steps 1: 94 percent / Heating 2: 66 percent / zinc dust, sodium chloride, water / 3 h / 150 °C / Heating 3: zinc dust, sodium chloride, water / 2 h / 240 °C View Scheme | |
Multi-step reaction with 2 steps 1: 47 percent / 1,2-dichloro-benzene / Heating 2: zinc dust, sodium chloride, water / 2 h / 240 °C View Scheme |
4-phenylnaphtho[2,3-c]furan-1,3-dione
A
1-phenylnaphthalene
B
fluoranthene
C
acephenanthrylene
D
aceanthrylene
Conditions | Yield |
---|---|
1.) 960 deg C, 0.02 mm, 2.) 180-200 deg C, 1.25 h; Yields of byproduct given; | A n/a B 60% C n/a D n/a |
at 960℃; under 0.02 Torr; Mechanism; Product distribution; var. temperature; |
Conditions | Yield |
---|---|
With silver (II) carbonate; triphenyl-arsane; palladium diacetate In 1,2-dichloro-ethane at 80℃; for 18h; Schlenk technique; Inert atmosphere; Sealed tube; | A 20% B 59% |
1,2-bis(4,4,5,5-tetramethyl-[1,3,2]dioxabororan-2-yl)benzene
1,8-diiodonaphthalene
fluoranthene
Conditions | Yield |
---|---|
With bis(tri-t-butylphosphine)palladium(0); water; caesium carbonate In 1,2-dimethoxyethane at 80℃; for 24h; Suzuki-Miyaura cross-coupling reaction; Inert atmosphere; | 56% |
8-(1-chloroethenyl)fluoranthene
A
fluoranthene
B
benzo[ghi]fluoranthene
Conditions | Yield |
---|---|
at 1200℃; under 0.01 Torr; | A 31% B 17% C 52% |
1,4-dibromonaphthalene
(2-bromophenyl)boronic acid
A
fluoranthene
B
indeno[123-cd]fluoranthene
Conditions | Yield |
---|---|
With tris(dibenzylideneacetone)dipalladium (0); 1,8-diazabicyclo[5.4.0]undec-7-ene; tricyclohexylphosphine In N,N-dimethyl-formamide at 155℃; for 48h; Suzuki coupling, Heck coupling; | A 35% B 51% |
Conditions | Yield |
---|---|
at 1100℃; for 0.000555556h; Product distribution; Mechanism; | A 47% B 14% |
fluoranthene
Conditions | Yield |
---|---|
With sodium hydroxide; tellurium; hydrazine; sodium tetrahydroborate; Aliquat 464 In benzene at 40℃; for 8h; sonication; | 30% |
2-(naphthalen-1-yl)benzenamine
phenylacetylene
A
1-phenylnaphthalene
B
fluoranthene
C
6-phenylbenzo[c]phenanthrene
Conditions | Yield |
---|---|
With fac-tris(2-phenylpyridinato-N,C2')iridium(III); tert.-butylnitrite In acetonitrile at 20℃; for 15h; Sealed tube; Irradiation; | A 30% B 20% C 24% |
3,9-Diethynyl-phenanthrene
A
fluoranthene
B
cyclopenta[c,d]pyrene
C
acephenanthrylene
Conditions | Yield |
---|---|
at 1025℃; under 0.01 Torr; Further byproducts given; | A 7% B 8% C 16% D 12% |
3,9-diacetylfluoranthene
A
fluoranthene
B
3-acetylfluoranthene
C
1-(fluoranthen-8-yl)ethanone
Conditions | Yield |
---|---|
With polyphosphoric acid (PPA) at 120℃; Temperature; Inert atmosphere; regioselective reaction; | A n/a B n/a C n/a D 11% |
Triangular [4]phenylene
A
fluoranthene
B
chrysene
C
benzo[ghi]fluoranthene
Conditions | Yield |
---|---|
at 1000℃; flash vacuum pyrolysis; | A 1% B 2.5% C 10% |
Conditions | Yield |
---|---|
With ethyl azidocarbonate In dichloromethane Heating; | 3% |
1-cyclohex-1-enyl-naphthalene
fluoranthene
Conditions | Yield |
---|---|
With chromium corundum at 475 - 530℃; | |
With palladium on activated charcoal at 420 - 455℃; |
Conditions | Yield |
---|---|
With chromium corundum at 475 - 530℃; | |
With palladium on activated charcoal at 420 - 455℃; |
Conditions | Yield |
---|---|
With aluminum (III) chloride In dichloromethane at 0 - 20℃; Friedel-Crafts Acylation; Inert atmosphere; | 100% |
With aluminum (III) chloride In dichloromethane at 0 - 20℃; for 5h; Friedel-Crafts Acylation; regioselective reaction; | 42% |
With carbon disulfide; aluminium trichloride |
fluoranthene
2,3-Dihydrofluoranthene
Conditions | Yield |
---|---|
With ammonia; sodium In tetrahydrofuran at -50℃; for 0.416667h; | 100% |
(i) Li, liq. NH3, (ii) NaOMe, MeOH; Multistep reaction; |
Conditions | Yield |
---|---|
With potassium dichromate | 99% |
With potassium dichromate | 99% |
With chromium(VI) oxide; acetic acid for 2h; Heating; | 98% |
fluoranthene
1,2,3,10b-tetrahydrofluoranthene
Conditions | Yield |
---|---|
With tetraethylammonium bromide In ethanol at 60℃; electrolysis, lead cathode; | 98% |
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate; methylamine hydrochloride; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 25℃; Irradiation; | 96% |
With hydrogenchloride; lithium perchlorate In N,N,N,N,N,N-hexamethylphosphoric triamide Mechanism; electrolysis; presence and absence of ethanol; |
fluoranthene
3-bromofluoranthene
Conditions | Yield |
---|---|
With bromine In nitrobenzene at 20℃; for 20h; | 94% |
With N-Bromosuccinimide In acetonitrile at 20℃; for 24h; | 80% |
With N-Bromosuccinimide In acetonitrile at 20℃; for 18h; | 75% |
fluoranthene
Conditions | Yield |
---|---|
With [mesitylenium]B(C6F5)4; benzene-d6 at 20℃; for 24h; Inert atmosphere; | 93% |
With d7-N,N-dimethylformamide; potassium tert-butylate at 170℃; for 1h; Microwave irradiation; | 75% |
fluoranthene
chromium(0) hexacarbonyl
(1-5,15-η(6)-fluoranthene)(tricarbonyl)chromium
Conditions | Yield |
---|---|
boiling;; | 91% |
boiling;; | 91% |
fluoranthene
Conditions | Yield |
---|---|
In tetrahydrofuran for 2h; | 87% |
Conditions | Yield |
---|---|
With tris(bipyridine)ruthenium(II) dichloride hexahydrate; 1-λ3-benzo[d][1,2]iodaoxol-3(1H)-one In 1,2-dichloro-ethane at 40℃; for 12h; Irradiation; Inert atmosphere; | 87% |
fluoranthene
Conditions | Yield |
---|---|
With iron(III) chloride; nitromethane at 50℃; for 15h; | 84% |
2,4,6-tri(4-pyridyl)-1,3,5-triazine
[Ru2(η6-p-cymene)2(C6H2O4)Cl2]
fluoranthene
silver trifluoromethanesulfonate
Conditions | Yield |
---|---|
In methanol byproducts: AgCl; a mixt. of complex and Ag-salt in methanol was stirred at room temp. for2 h, filtered, triazine-compound and aromatic molecule were added, the mixt. was stirred at room temp. for 24 h; the solvent was removed under vac., the residue was taken up in CH2Cl2, filtered, concd., diethyl ether was added; elem. anal.; | 81% |
2,4,6-tri(4-pyridyl)-1,3,5-triazine
[((hexamethylbenzene)RuCl)2(3,6-dichloro-2,5-dihydroxy-1,4-benzoquinonato(2-))]
fluoranthene
silver trifluoromethanesulfonate
Conditions | Yield |
---|---|
In methanol byproducts: AgCl; a mixt. of complex and Ag-salt in methanol was stirred at room temp. for2 h, filtered, triazine-compound and aromatic molecule were added, the mixt. was stirred at room temp. for 24 h; the solvent was removed under vac., the residue was taken up in CH2Cl2, filtered, concd., diethyl ether was added; elem. anal.; | 77% |
fluoranthene
N-fluorobis(benzenesulfon)imide
Conditions | Yield |
---|---|
With 6,6'-dimethyl-2,2'-bipyridine; copper(I) bromide In 1,2-dichloro-ethane at 70℃; for 12h; Reagent/catalyst; Schlenk technique; Inert atmosphere; regioselective reaction; | 77% |
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid; silica gel In dichloromethane at 25℃; for 24h; Nitration; | A 76% B n/a |
With nitric acid; acetic acid |
2,4,6-tri(4-pyridyl)-1,3,5-triazine
Ru2(p-cymene)2(μ4-2,5-dichloro-1,4-benzoquinonato)Cl2
fluoranthene
silver trifluoromethanesulfonate
Conditions | Yield |
---|---|
In methanol byproducts: AgCl; a mixt. of complex and Ag-salt in methanol was stirred at room temp. for2 h, filtered, triazine-compound and aromatic molecule were added, the mixt. was stirred at room temp. for 24 h; the solvent was removed under vac., the residue was taken up in CH2Cl2, filtered, concd., diethyl ether was added; elem. anal.; | 75% |
Conditions | Yield |
---|---|
With o-tetrachloroquinone; silver trifluoromethanesulfonate; palladium diacetate at 50℃; for 14h; Inert atmosphere; regioselective reaction; | 74% |
fluoranthene
A
3-nitrofluoranthene
B
1,2-dinitrofluoranthene
C
1-Nitrofluoranthene
D
2-nitrofluoranthene
E
1,3-dinitrofluoranthene
Conditions | Yield |
---|---|
With dinitrogen tetraoxide; Nitrogen dioxide In tetrachloromethane at 24.5 - 25.5℃; Product distribution; Mechanism; other temperatures, other solvents, other additives; | A 14% B 3% C 1% D 73% E 9% |
fluoranthene
A
3-nitrofluoranthene
B
1,2-dinitrofluoranthene
C
2-nitrofluoranthene
D
1,3-dinitrofluoranthene
Conditions | Yield |
---|---|
With Nitrogen dioxide In tetrachloromethane at 24.5 - 25.5℃; Further byproducts given; | A 14% B 3% C 73% D 9% |
With dinitrogen tetroxide; Nitrogen dioxide; tetrabutylammonium nitrate In tetrachloromethane at 24.5 - 25.5℃; Further byproducts given; | A 14% B 13% C 58% D 14% |
With dinitrogen tetroxide; Nitrogen dioxide; tetrabutylammonium nitrate In tetrachloromethane at 24.5 - 25.5℃; Further byproducts given; | A 12% B 13% C 58% D 17% |
With dinitrogen tetraoxide; Nitrogen dioxide In tetrachloromethane at 25℃; Further byproducts given; | A 23.7 % Chromat. B 12.3 % Chromat. C 53.7 % Chromat. D 7.4 % Chromat. |
Conditions | Yield |
---|---|
With o-tetrachloroquinone; silver trifluoromethanesulfonate; palladium diacetate In 1,2-dichloro-ethane at 80℃; for 2h; Inert atmosphere; regioselective reaction; | 71% |
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