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inquiryWelcome 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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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
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Product Description Product website: http://www.finerchem.com/pro01en/id/1418.html Product Name 9-Anthraldehyde
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inquiryName: 9-Anthraldehyde Synonyms: 9-Anthracenecarboxaldehyde CAS: 642-31-9 MF: C15H10O Appearance: white powder Storage:Store in cool and dry place, away from sun light. Package: 25kgs/drum Application: Pharmaceutical Intermediate Transportation:By
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inquiryOur company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At present
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inquiryHenan 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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Best quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
With our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufacturin
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inquiryCompany Introduction 1. Established in 2005, with two independent business divisions: Fine chemicals division; Pharmaceutical division. 2. Main product: Optical brightener Textile auxiliary Dye stuff Pigments
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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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
Product name: 9-Anthraldehyde CAS No.: 642-31-9 Molecule Formula:C15H10O Molecule Weight:206.24 Purity: 99.0% Package: 25kg/drum Description:Yellow crystalline powder Manufacture Standards:Enterprise Standard TESTING ITEMS
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inquiryOur company was built in 2009 with an ISO certificate.In the past 5 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so
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inquiry9-Anthraldehyde Chemical Properties Melting point 103-105 °C (lit.) Boiling point 305.09°C (rough estimate) density 1.0701 (rough estimate) refractive index 1.6324 (estimate) storage temp. Store below +30°C. solubility
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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
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
C-5304 A-9-A,9-Anthraldehyde M.F:C15H10O Melting Point:102~105Deg.C Loss on Drying 1%Max Measurement: 430×570mm Use: Used as inter…Appearance:Yellow crystalline powder Package:25kgs/inner plastic carton drum
Stock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
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inquiryhigh 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
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1.High quality : the purity is 99% min . through multiple producing procedures. 2.Competitive price : low price because of our skilled production technolpgy ,save the production cost at most , and give big profit room to our customers184.Safe and fa
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inquiryConditions | Yield |
---|---|
With potassium carbonate; chlorobenzene In toluene at 105℃; for 24h; | 100% |
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In N,N-dimethyl-formamide at 23 - 25℃; for 7.5h; | 100% |
With polymeric complex of oxodiperoxochromium(VI) compound and pyrazine (Pyz-CrO5)n In dichloromethane for 0.6h; Ambient temperature; | 99% |
anthracene
trifluoromethanesulphonyloxy-methylene-N,N-dimethyliminium trifluoromethanesulphonate
9-anthracene aldehyde
Conditions | Yield |
---|---|
In dichloromethane at 37℃; for 48h; | 98% |
9-anthracenealdehyde oxime
9-anthracene aldehyde
Conditions | Yield |
---|---|
With cethyltrimethylammonium permanganate In dichloromethane at 25℃; for 0.25h; | 96% |
With polymeric complex of oxodiperoxochromium(VI) compound and pyrazine (Pyz-CrO5)n In dichloromethane for 0.9h; Ambient temperature; | 90% |
Conditions | Yield |
---|---|
With titanium tetrachloride In dichloromethane at 0 - 20℃; | 95% |
Conditions | Yield |
---|---|
With tetra(n-butyl)ammonium hydroxide; water at 150℃; for 0.166667h; Reagent/catalyst; Microwave irradiation; Green chemistry; | A n/a B 93% |
Conditions | Yield |
---|---|
With silica gel; trichlorophosphate for 0.025h; Formylation; Microwave irradiation (300 W); | 92% |
With trichlorophosphate In chlorobenzene for 2h; Schlenk technique; Inert atmosphere; Reflux; | 85% |
With trichlorophosphate In 1,2-dichloro-ethane at 40℃; for 1h; Vilsmeier Haack formylation; ultrasound irradiation; | 80% |
Conditions | Yield |
---|---|
With sodium periodate In water; ethyl acetate; acetonitrile at 0℃; for 3h; | 92% |
With aluminum oxide; potassium permanganate In dichloromethane at 20℃; for 48h; | 30% |
With isobutyraldehyde In acetonitrile at 80℃; for 24h; |
potassium cyanide
9-cyano-10-anthracenocarboxaldehyde
A
9-cyanoanthracene
B
9-anthracene aldehyde
Conditions | Yield |
---|---|
In ethanol; water at 80℃; for 31h; | A 91% B 9.4% |
9-(dipropionyloxymethyl)anthracene
9-anthracene aldehyde
Conditions | Yield |
---|---|
With tetra-N-butylammonium tribromide In methanol at 20℃; for 9h; | 91% |
C18H16S2
9-anthracene aldehyde
Conditions | Yield |
---|---|
With eosin y In water; acetonitrile at 20℃; for 2h; Irradiation; | 91% |
Conditions | Yield |
---|---|
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In water; acetic acid for 0.5h; Heating; | 90% |
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In water; acetic acid for 0.5h; Product distribution; Heating; other alkyl- and cycloalkylene-aromatic hydrocarbons; | 90% |
With acetic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone In water Reflux; | 87% |
With nickel-doped graphene carbon nitride nanoparticles; air In ethanol at 25℃; for 8h; Irradiation; Green chemistry; | 85% |
Conditions | Yield |
---|---|
With trichlorophosphate In 1,2-dichloro-benzene at 89.84 - 94.84℃; for 2h; Vielsmeyer reaction; | 89% |
With trichlorophosphate In 1,2-dichloro-benzene at 0 - 90℃; | 84% |
With trichlorophosphate In 1,2-dichloro-benzene at 100℃; for 1h; | 81% |
9-(azidomethyl)anthracene
9-anthracene aldehyde
Conditions | Yield |
---|---|
With MoO2(S2CNEt2)2; oxygen In water for 10h; Heating; | 88% |
Stage #1: 9-(azidomethyl)anthracene With sodium hydride In dimethyl sulfoxide; mineral oil at 20℃; for 4h; Inert atmosphere; Stage #2: With water In dimethyl sulfoxide; mineral oil for 0.25h; Inert atmosphere; | 72% |
9-anthracene aldehyde
Conditions | Yield |
---|---|
With ethanol In dimethyl sulfoxide at 30℃; sonic bath; | 86% |
α,α-diacetoxy-9-methylanthracene
9-anthracene aldehyde
Conditions | Yield |
---|---|
With tetra-N-butylammonium tribromide In methanol at 20℃; for 12h; | 85% |
With carbon tetrabromide In acetonitrile for 8h; Heating; | 75% |
With indium(III) chloride In water at 20℃; |
9-anthracenecarboxaldehyde dimethyl acetal
9-anthracene aldehyde
Conditions | Yield |
---|---|
perchloric acid In methanol; water at 25 - 30℃; for 0.5h; | 82% |
With water In methanol at 25 - 30℃; for 0.5h; | 82% |
With iron(III) In dimethylsulfoxide-d6 |
Conditions | Yield |
---|---|
With potassium carbonate In chloroform at 20℃; for 24h; Irradiation; Inert atmosphere; | 82% |
9-anthracene aldehyde
Conditions | Yield |
---|---|
With dibenzoyl peroxide | 80% |
bromo-9 methoxymetyl-10 anthracene
A
9-(methoxymethyl)anthracene
B
9,10-phenanthrenequinone
C
9-anthracene aldehyde
Conditions | Yield |
---|---|
With potassium phenolate In N,N,N,N,N,N-hexamethylphosphoric triamide at 100℃; for 4h; | A 4% B 5% C 77% |
(anthracen-9-yl)methyl methyl sulfide
1,4-diphenyl-but-2-yne-1,4-dione
A
1,2,4,5-tetrabenzoylbenzene
D
9-anthracene aldehyde
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 15h; Diels-Alder Cycloaddition; Reflux; | A 1% B 76% C 1% D 10% |
tert-butylisonitrile
9-Bromoanthracene
9-anthracene aldehyde
Conditions | Yield |
---|---|
Stage #1: tert-butylisonitrile; 9-Bromoanthracene With triethylsilane; palladium diacetate; sodium carbonate; CyJohnPhos In N,N-dimethyl-formamide at 65℃; for 8h; Inert atmosphere; Sealed tube; Green chemistry; Stage #2: With water Green chemistry; | 67% |
9-hydroxymethylanthracene
A
9,10-phenanthrenequinone
B
9-anthracene aldehyde
Conditions | Yield |
---|---|
With osmium(VIII) oxide; trimethylamine-N-oxide In tetrahydrofuran; pyridine; water at 65℃; | A 64% B n/a |
(anthracen-9-yl)methyl methyl sulfide
dimethyl acetylenedicarboxylate
A
(anthracen-9-yl)methyl acetate
D
1,2-bis(methoxycarbonyl)-1-methylthioethylene
E
9-anthracene aldehyde
Conditions | Yield |
---|---|
With acetic acid for 3h; Diels-Alder Cycloaddition; Reflux; | A 63% B 1% C 1% D 18% E 6% |
anthracenylmethyl chloride
9-anthracene aldehyde
Conditions | Yield |
---|---|
With manganese(IV) oxide In chloroform at 60℃; for 4h; | 60% |
2-(3-indole)-ethanol
9-anthracenecarboxaldehyde dimethyl acetal
B
9-anthracene aldehyde
Conditions | Yield |
---|---|
With camphor-10-sulfonic acid In chloroform for 16h; Reagent/catalyst; Solvent; Pictet-Spengler Synthesis; Schlenk technique; Inert atmosphere; | A 60% B 13 %Spectr. |
Conditions | Yield |
---|---|
With titanium tetrachloride In chlorobenzene at 0 - 20℃; for 12h; | 48% |
<9,10-dihydro-10-(methoxymethylene)-9-trimethylsilyl>antracene
9-anthracene aldehyde
Conditions | Yield |
---|---|
With silica gel In hexane for 20h; | 47% |
(anthracen-9-yl)methyl methyl sulfide
dimethyl acetylenedicarboxylate
D
9-anthracene aldehyde
Conditions | Yield |
---|---|
In 5,5-dimethyl-1,3-cyclohexadiene for 10h; Solvent; Diels-Alder Cycloaddition; Reflux; | A 10% B 44% C 1% D 9% |
(anthracen-9-yl)methyl methyl sulfide
1,4-diphenyl-but-2-yne-1,4-dione
A
(anthracen-9-yl)methyl acetate
B
1,2,4,5-tetrabenzoylbenzene
E
5,6,-11,12-tetrahydro-4b,12[1',2']:6,10b[1'',2'']dibenzenochrysene
F
2-(methylthio)-1,4-diphenylbut-2-ene-1,4-dione
G
9-anthracene aldehyde
Conditions | Yield |
---|---|
With acetic acid for 13h; Diels-Alder Cycloaddition; Reflux; | A 14% B 1% C 42% D 2% E 6% F 10% G 19% |
chloro-trimethyl-silane
9-(methoxymethyl)anthracene carbanion
A
9-neopentylantracene
B
<9,10-dihydro-10-(methoxymethylene)-9-trimethylsilyl>antracene
C
9-anthracene aldehyde
Conditions | Yield |
---|---|
A 36% B 40% C 16% | |
A 36% B 40% C n/a |
Conditions | Yield |
---|---|
With cobalt(II) 2,9,16,23-phthalocyanine tetrasulfonic acid In water; acetonitrile at 20℃; under 760.051 Torr; for 150h; UV-irradiation; | 100% |
With (bipyH2)-CrOCl5 In dichloromethane at 28 - 30℃; for 12h; | 95% |
With dihydrogen peroxide In water; acetonitrile at 45℃; for 1h; chemoselective reaction; | 78% |
2,4,5,7-tetranitro-9H-fluorene
9-anthracene aldehyde
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; | 100% |
Conditions | Yield |
---|---|
With sodium hydroxide In dichloromethane for 2h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
at 20℃; under 750.06 Torr; Solid phase reaction; gas-solid reaction; | 100% |
In methanol for 9h; Reflux; | 84% |
Conditions | Yield |
---|---|
at 20℃; under 750.06 Torr; Solid phase reaction; gas-solid reaction; | 100% |
In tetrahydrofuran; methanol | |
In ethanol |
Conditions | Yield |
---|---|
With acetic acid In ethanol Heating; | 100% |
In methanol; N,N-dimethyl-formamide for 4h; Heating; | 94% |
With acetic acid In methanol for 12h; Reflux; | 85.32% |
Conditions | Yield |
---|---|
With acetic acid In ethanol Heating; | 100% |
In methanol; dichloromethane for 4h; Heating; | |
In methanol; dichloromethane for 4h; Reflux; |
1,2-diamino-benzene
9-anthracene aldehyde
N1-(anthracene-9-methylene)benzene-1,2-diamine
Conditions | Yield |
---|---|
With acetic acid In toluene for 2h; Reflux; | 100% |
With acetic acid In toluene for 2h; Reflux; | 94% |
In ethanol at 20℃; for 6h; | 88% |
In methanol at -5℃; for 6h; | 70% |
(4-(but-3-en-1-yloxy)phenyl)methanamine
9-anthracene aldehyde
AnCH=NC6H4OCH2CH2CH=CH2
Conditions | Yield |
---|---|
In toluene Molecular sieve; Reflux; | 100% |
Conditions | Yield |
---|---|
With L-proline In ethanol at 20℃; | 100% |
Conditions | Yield |
---|---|
With acetic acid In toluene for 2h; Reflux; | 100% |
Conditions | Yield |
---|---|
With sodium tetrahydroborate In ethanol at 20℃; for 0.5h; | 99% |
With sodium tetrahydroborate In ethanol at 20℃; for 0.5h; | 99% |
With sodium tetrahydroborate In tetrahydrofuran for 2h; Reflux; | 99% |
Conditions | Yield |
---|---|
With cyclohexylamine at 120℃; Microwave irradiation; | 99% |
With piperdinium acetate at 90℃; for 2.5h; Knoevenagel Condensation; Inert atmosphere; | 99% |
With ammonium acetate; acetic acid for 6h; Reflux; | 52% |
9-anthracene aldehyde
benzylamine
1-(anthracen-9-yl)-N-benzylmethanimine
Conditions | Yield |
---|---|
With magnesium sulfate In tetrahydrofuran at 20℃; for 2h; Inert atmosphere; | 99% |
With magnesium sulfate; triethylamine In dichloromethane for 120h; Ambient temperature; | 52% |
In toluene for 24h; Schiff Reaction; Reflux; Dean-Stark; | 26% |
(S)-1-phenyl-ethylamine
9-anthracene aldehyde
(S)-9-(anthracen-9-ylmethylene)-α-phenylethylamine
Conditions | Yield |
---|---|
With potassium carbonate In ethanol; water at 20℃; for 12h; | 99% |
In tetrahydrofuran; ethanol Heating; | |
With acetic acid In toluene for 6h; Reflux; |
(S)-(+)-2-(N-methylamino)-3-phenylpropanol
9-anthracene aldehyde
(2S,4S)-2-(9-anthracenyl)-3-methyl-4-benzyl oxazolidine
Conditions | Yield |
---|---|
With magnesium sulfate In tetrahydrofuran at 20℃; for 6h; | 99% |
Conditions | Yield |
---|---|
at 20℃; for 0.5h; Glovebox; | 99% |
With C32H39Br2MgN2(1-)*C16H32LiO4(1+) In chloroform-d1 at 20℃; for 3h; Inert atmosphere; Glovebox; | 99% |
With Zr(IV) metal-organic framework with 1,4-benzenedicarboxylate in anhydrous form In dichloromethane at 40℃; for 46h; Inert atmosphere; Reflux; | 50% |
9-anthracene aldehyde
benzyl alcohol
allyl-trimethyl-silane
10-(1-(benzyloxy)but-3-enyl)anthracene
Conditions | Yield |
---|---|
With perchloric acid supported on silica gel In dichloromethane; acetonitrile at 20℃; for 0.5h; Hosomi-Sakurai reaction; | 99% |
With 50 wt% silicomolybdic acid/SiO2 In acetonitrile at 20℃; for 1h; Hosomi-Sakurai reaction; | 82% |
9-anthracene aldehyde
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane
2-(anthracene-9-ylmethoxy)pinacolborane
Conditions | Yield |
---|---|
With C27H44AlN3 In benzene at 20℃; for 0.333333h; Inert atmosphere; Glovebox; | 99% |
With catalyst:C4H9Mg(2,6-iPr2C6H3NCCH3)CH In benzene-d6 pinacolborane reacted with aldehyde in C6D6 at 25°C catalized by nBuMg(2,6-iPrC6H3NCCH3)2CH 0.1-0.5 mol% for 0.75 h; | 84% |
With [HC{(Me)CN(2,6-iPr2C6H3)}2MgnBu] In benzene-d6 at 20℃; for 0.75h; Inert atmosphere; Sealed tube; | 96 %Spectr. |
Conditions | Yield |
---|---|
Stage #1: (1-bromovinyl)triisopropylsilane With n-butyllithium In tetrahydrofuran at -78℃; for 1h; Stage #2: 9-anthracene aldehyde In tetrahydrofuran at -78℃; for 1h; | 99% |
Conditions | Yield |
---|---|
With potassium phosphate; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; C22H19OP In 1,4-dioxane at 70℃; Inert atmosphere; enantioselective reaction; | 99% |
C6H5NHBO2C2(CH3)4
9-anthracene aldehyde
(E)-N-(9-Anthrylmethylene)benzenamine
Conditions | Yield |
---|---|
In benzene-d6 at 25℃; for 1h; Inert atmosphere; Schlenk technique; | 99% |
9-anthracene aldehyde
malononitrile
2‐(anthracen‐9‐ylmethylene)malononitrile
Conditions | Yield |
---|---|
With C88H68Cl4Hg2N4O4P4 In methanol at 60℃; for 4h; Catalytic behavior; Knoevenagel Condensation; | 98% |
With triethylamine In ethanol at 20℃; for 2h; | 90% |
With Zn(1+)*C5H8NO2(1-) In water at 80℃; for 0.166667h; Knoevenagel Condensation; | 84% |
9-anthracene aldehyde
9-trans-styryl-anthracene
Conditions | Yield |
---|---|
With crosslinked polymer-supported phosphonium salt of benzyl chloride; cetyltrimethylammonim bromide In sodium hydroxide; dichloromethane for 2h; Product distribution; Ambient temperature; without catalysts; other polymer supported phosphonium salt; | 98% |
Multi-step reaction with 2 steps 1: NaOAc, Ac2O / 145 - 150 °C 2: (i) Cu, quinoline, (ii) I2, xylene View Scheme |
Conditions | Yield |
---|---|
With sodium hydroxide; cetyltrimethylammonim bromide In dichloromethane for 2h; Ambient temperature; | 98% |
aminomethyl-dimethyl-phosphine oxide
9-anthracene aldehyde
Conditions | Yield |
---|---|
In benzene at 20℃; for 4h; | 98% |
9-anthracene aldehyde
Conditions | Yield |
---|---|
Stage #1: 9-anthracene aldehyde; chitosan, intrinsic viscosity 230 ml/g, fraction of N-acetylated units 0.09 In methanol; acetic acid at 20℃; for 24h; Stage #2: With sodium cyanoborohydride at 20℃; for 12h; | 98% |
Conditions | Yield |
---|---|
With palladium diacetate; potassium carbonate In ethyl acetate at 150℃; under 12929 Torr; for 0.833333h; Microwave irradiation; Molecular sieve; | 98% |
With palladium nanoparticles supported on fibrous silica In cyclohexane at 130℃; for 20h; Molecular sieve; | 98% |
With palladium diacetate In cyclohexane at 140℃; for 24h; Molecular sieve; air; | 97% |