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Cas:615-13-4
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inquiryProduct description: Product name 2-Indanone CAS number 615-13-4 Assay ≥99% Appearance White crystal Capacity 200mt/year Application Organic intermediate More inform
hebei yanxi chemical 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 research and developm
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inquiryFactory supply 2-Indanone CAS 615-13-4 with good quality Company profile Wuhan Fortuna Chemical Co.,Ltd established in 2006, is a big integrative chemical enterprise being engaged in Pharmaceutical & its intermediates, Food/Feed additives, F
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inquiryItems Standard Result Appearance White or off white crystal White crystal Melting point 56℃~
Cas:615-13-4
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inquiryHigh quality Promptly delivery Good price T he company has advanced technology, as well as a large number of excellent R & D team, to provide customers from the grams to one hundred kilograms and tons of high-quality products, competitive
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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Cangzhou Enke Pharma Tech Co.,ltd. is located in Cangzhou City, Hebei province ,where is a famous petroleum chemical industry city in China. Enke Pharma a high-tech enterprise ,and we are dedicated to developing and manufacturing new ap
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
Cas:615-13-4
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inquiryOur 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
Stock products, own laboratory Appearance:Crystals or Powder Storage:2-8°C Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
Cas:615-13-4
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inquiry2-Indanone Basic information Product Name: 2-Indanone Synonyms: 1,3-dihydro-2h-inden-2-on;1,3-Dihydro-2H-inden-2-one;2H-Inden-2-one,1,3-dihydro-;2-Hydrindone;2-Oxohydrindene;2-OXOINDANE;
Cas:615-13-4
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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:615-13-4
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inquiryName indan-2-one Other name 2-Indanone; 1,3-Dihydro-2H-inden-2-one; 2H-Inden-2-one, 1,3-dihydro- CAS 615-13-4
1.No Less 8 years exporting experience. Clients can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specialized
Cas:615-13-4
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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,
Cas:615-13-4
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inquiry2-Indanone CAS:615-13-4 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 intermediates,
Cas:615-13-4
Min.Order:1 Gram
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
Product Detail Minimum Order Qty. 10 Gram
Cas:615-13-4
Min.Order:10 Gram
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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
Our Advantage: high quality with competitive price High quality standard: BP/USP/EP Enterprise standard All purity customized Fast and safe delivery We have reliable forwarder who can help us deliver our goods more fast and safe. We
Cas:615-13-4
Min.Order:10 Kilogram
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inquiryOur advantages: 1. All inquiries will be replied within 12 hours. 2. Dedication to quality, supply & service. 3. Strictly on selecting raw materials. 4. Reasonable & competitive price, fast lead time. 5. Sample is available for your eva
Cas:615-13-4
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inquiryAppearance:Light yellow to yellow-brown Crystals or Powder Storage:2-8°C Application:2-Indanone undergoes TiCl4-Mg mediated coupling with CHBr3 to yield dibromomethyl carbinol. It reacts with 5,5-dimethyl-3-pyrazolidinone to yield 5,5-dime
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
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 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:615-13-4
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquiryadvantage: 1. The best price, satisfactory quality; 2. customers have the right to choose the delivery of parcels (EMS, DHL, FedEx, UPS); 3. customers have the right to choose from the recent effective packaging methods of their products packaging
We are one of a few suppliers that can offer custom synthesis service of this product We are specialized in custom synthesis, chemical/pharmaceutical/ pesticides outsourcing and contract research. We are committed to prov
Cas:615-13-4
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inquiryFormic acid 1H-inden-2-yl ester
2-indanone
Conditions | Yield |
---|---|
With hydrogenchloride In tetrahydrofuran; water for 7h; Ambient temperature; | 98% |
Conditions | Yield |
---|---|
With oxygen; cobalt(II) acetate; isobutyraldehyde In acetonitrile at 60℃; for 1h; | 97% |
Stage #1: 1-indene With dihydrogen peroxide; acetic anhydride; acetic acid at 40 - 55℃; for 14h; Green chemistry; Stage #2: With sulfuric acid In water at 5 - 50℃; for 3h; Green chemistry; | 97.1% |
With chloropyridinecobaloxime(III); water; 9-(2-mesityl)-10-methylacridinium perchlorate In acetonitrile at 20℃; for 24h; Wacker Oxidation; Inert atmosphere; Schlenk technique; Irradiation; regioselective reaction; | 80% |
Conditions | Yield |
---|---|
With Dowex-50W In water for 0.5h; Heating; | 95% |
With pentacarbonyliron In benzene for 3h; Irradiation; | 85% |
With indium(III) chloride In tetrahydrofuran at 25℃; for 0.75h; Rearrangement; | 85% |
2-indanone
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene for 0.25h; Heating; | 95% |
With sulfuric acid | |
Multi-step reaction with 2 steps 1: thionyl chloride; pyridine / benzene / 3 h 2: acetonitrile / 2 h / Irradiation; Inert atmosphere View Scheme |
2-indanone
Conditions | Yield |
---|---|
With ammonium cerium(IV) nitrate In acetone for 3.66667h; reag. added in three portions; | 90% |
(orthoquinodimethane)tricarbonyliron
2-indanone
Conditions | Yield |
---|---|
With ammonium cerium(IV) nitrate In acetone anh. (NH4)2Ce(NO3)6 was added portionwise to a stirred soln. of (C8H8)Fe(CO)3 in anh. acetone (after 50 min and 70 min), after 100 min of reaction addn. of H2O, mixture was extracted with CH2Cl2 (4 times), extract was dried (MgSO4), solvent evaporation;; filtration through a short column of silica gel; white crystals with m.p. 54-55°C were obtained;; | 90% |
1-(trimethylsilyl)-3-phenylprop-1-yne
2-indanone
Conditions | Yield |
---|---|
With 8-isopropyl-quinoline-N-oxide; [Au(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)(NTf2)] In fluorobenzene at 60℃; | 90% |
2-indanone
Conditions | Yield |
---|---|
With 8-isopropyl-quinoline-N-oxide; [Au(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)(NTf2)] In fluorobenzene at 60℃; | 90% |
dimethyl(phenyl)(3-phenylprop-1-yn-1-yl)silane
2-indanone
Conditions | Yield |
---|---|
With 8-isopropyl-quinoline-N-oxide; [Au(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)(NTf2)] In fluorobenzene at 60℃; | 90% |
Conditions | Yield |
---|---|
With nitrobenzene In acetonitrile for 24h; | A 85% B 9% |
With p-nitrobenzene iodide In acetonitrile for 18h; | A 40% B 50% |
malononitrile
A
2-indanone
C
[3aS-[2(3'aR*,8'aS*),3a,8a]]methylenebis[3a,8a-dihydro-8H-indeno[1,2-d]oxazole]
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid In dichloromethane -40 deg C to room t.; Yields of byproduct given; | A n/a B 80% C n/a |
With trifluorormethanesulfonic acid In dichloromethane Product distribution; -40 deg C to room t.; reactions with var. dinitriles; | A n/a B 10% C 60% |
With trifluorormethanesulfonic acid In dichloromethane -40 deg C to room t.; | A n/a B 10% C 60% |
Conditions | Yield |
---|---|
With dimethyl sulfoxide; triethylamine In dichloromethane at -40 - 20℃; for 8h; | 79% |
With [Cu6(pyridine-2-thiolate)6]; potassium hydroxide In toluene at 70℃; for 24h; Schlenk technique; Glovebox; Inert atmosphere; | 78% |
With [Cu6(SC5H4N)6]; potassium hydroxide In toluene at 70℃; for 24h; Glovebox; Inert atmosphere; | 78% |
propargyl benzene
2-indanone
Conditions | Yield |
---|---|
With 2-(tert-butyl)-6-chloropyridine 1-oxide; C45H57AuF6NO9PS2 In chloroform at 60℃; for 2h; Reagent/catalyst; Temperature; Time; | 77% |
With 3,5-dicholoropyridine N-oxide; [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I) In dichloromethane at 20℃; for 8h; Reagent/catalyst; | 43% |
Conditions | Yield |
---|---|
With bismuth(III) nitrate; Montmorillonite K 10; copper diacetate In water; acetone for 3h; Heating; | 76% |
With bismuth(lll) trifluoromethanesulfonate; bismuth(III) bromide In water; acetone; acetonitrile for 0.7h; Heating; | |
With gold(III) tribromide; dimethylglyoxal In ethanol; water at 20℃; for 15h; pH=7; | 100 %Spectr. |
C
2-indanone
Conditions | Yield |
---|---|
With 8-isopropyl-quinoline-N-oxide; [Au(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)(NTf2)] In fluorobenzene at 60℃; Reagent/catalyst; | A 20% B 75% C 5% |
2-indanone
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In tetrahydrofuran for 0.166667h; Inert atmosphere; | 68% |
With tetrabutyl ammonium fluoride In tetrahydrofuran | 68% |
2-nitrothiophene
1-indene
A
2-nitro-indene
B
2-(o-tolyl)-2-oxo-ethanale
C
2-indanone
D
2-(2-thienyl)indene
Conditions | Yield |
---|---|
In acetonitrile for 1h; | A 20% B 6% C 8% D 66% |
1-diazo-3-phenyl-2-propanone
A
cyclohepta-2,4,6-trienylbenzylketone
B
2-indanone
Conditions | Yield |
---|---|
With rhodium(II) trifluoroacetate dimer In benzene at 22℃; | A 64% B 18% |
1-diazo-3-phenyl-2-propanone
benzene
A
cyclohepta-2,4,6-trienylbenzylketone
B
2-indanone
Conditions | Yield |
---|---|
With rhodium(II) trifluoroacetate dimer at 22℃; | A 64% B 18% |
Indan-2-spiro-3'-(1',2',4'-trioxane)-6'-spiro-1''-cyclohexane
A
cyclohexanone
B
2-indanone
Conditions | Yield |
---|---|
In decane at 190℃; for 8h; | A n/a B n/a C 53% |
1-diazo-3-phenyl-2-propanone
benzene
A
2-indanone
B
1,3-Diphenylpropanone
Conditions | Yield |
---|---|
rhodium(II) trifluoroacetate dimer for 1h; Ambient temperature; | A 49% B 31% |
Conditions | Yield |
---|---|
With sodium tetracarbonyl cobaltate In tetrahydrofuran for 8h; Heating; | 46% |
Conditions | Yield |
---|---|
With dirhodium tetraacetate In dichloromethane | 42% |
dirhodium tetraacetate In dichloromethane for 24h; | 42% |
B
2-indanone
Conditions | Yield |
---|---|
With PPA at 100℃; for 3h; | A 39% B 13% |
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid In dichloromethane -40 deg C to room t.; Yield given; | A n/a B n/a C 30% |
With trifluorormethanesulfonic acid In dichloromethane -40 deg C to room t.; Yields of byproduct given; | A n/a B n/a C 30% |
1-indene
A
(1S,2R)-epoxyindane
B
2-indanone
Conditions | Yield |
---|---|
With potassium phosphate; Leifsonia sp. S749 alcohol dehydrogenase; Rhodococcus sp. ST-10 styrene monooxygenase; NAD+; oxygen; isopropyl alcohol; flavin adenine dinucleotide at 25℃; for 24h; pH=7.5; Microbiological reaction; enantioselective reaction; | A 21% B 27% |
Conditions | Yield |
---|---|
With oxygen In acetonitrile at 25℃; for 24h; Sealed tube; Irradiation; Green chemistry; | A 26% B 10% |
2,3-dihydro-1H-indene 2,3-oxide
(+/-)-N-(cis-2-hydroxy-indan-1-yl)-acetamide
(+/-)-N-(trans-2-hydroxy-indan-1-yl)-acetamide
C
2-indanone
Conditions | Yield |
---|---|
With sulfuric acid; acetonitrile at -40℃; Further byproducts given; | A n/a B n/a C 12% D n/a |
2,3-dihydro-1H-indene 2,3-oxide
acetonitrile
(+/-)-N-(cis-2-hydroxy-indan-1-yl)-acetamide
(+/-)-N-(trans-2-hydroxy-indan-1-yl)-acetamide
C
2-indanone
Conditions | Yield |
---|---|
With sulfuric acid at -40℃; Mechanism; | A n/a B n/a C 12% D n/a E n/a |
Conditions | Yield |
---|---|
With N-(benzenesulfonyl)-3-phenyloxaziridine In chloroform at 60℃; for 3h; | A 40 % Chromat. B 10% |
Stage #1: 1-indene With manganese(II) acetate; 1-bicyclo[2.2.1]hept-5-en-2-yl-CH2-4,7-diMe[1,4,7]triazonane In methanol; acetone at 0℃; for 0.25h; Stage #2: With oxalic buffer; dihydrogen peroxide In methanol; acetone at 0 - 2℃; for 4.5h; Further stages.; | |
With 3H-2,1-benzoxaselenole Se-oxide; dihydrogen peroxide; magnesium sulfate; trifluoroacetic acid In dichloromethane at 20℃; for 13h; | |
With Ti0.85V0.15O2; dihydrogen peroxide In methanol at 20℃; for 2h; |
Conditions | Yield |
---|---|
With sodium tetrahydroborate In ethanol at 0℃; Inert atmosphere; | 100% |
With methanol; sodium tetrahydroborate at 25℃; for 1h; | 98% |
With tetrakis[3,5-bis(trifluoromethyl)phenyl]boric acid bis(diethyl ether) complex; C32H63CoNP2Si; hydrogen In tetrahydrofuran at 60℃; under 760.051 Torr; for 48h; | 97% |
Conditions | Yield |
---|---|
In benzene for 3h; Condensation; Heating; | 100% |
With toluene-4-sulfonic acid In benzene for 4h; Heating; | 79% |
In toluene at 70℃; for 24h; Molecular sieve 4Å; | 48% |
1-chloroethyl p-tolyl sulfoxide
2-indanone
2-<1-chloro-1-(p-tolylsulfinyl)ethyl>-2-indanol
Conditions | Yield |
---|---|
at -70℃; | 100% |
With n-butyllithium; diisopropylamine In tetrahydrofuran at -65℃; for 0.416667h; | 93% |
With lithium diisopropyl amide 1.) THF; Multistep reaction; | |
With lithium diisopropyl amide 1) THF, -60 deg C, 10 min; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
In tetrahydrofuran | 100% |
In chloroform Ambient temperature; | 72% |
2-indanone
[(S)-3-(Indan-2-ylamino)-2-oxo-piperidin-1-yl]-acetic acid benzyl ester
Conditions | Yield |
---|---|
With DCE; sodium tris(acetoxy)borohydride; triethylamine Ambient temperature; | 100% |
trimethylsilyl cyanide
2-indanone
2-[(trimethylsilyl)oxy]-2,3-dihydro-1H-indene-2-carbonitrile
Conditions | Yield |
---|---|
With copper(II) bis(trifluoromethanesulfonate) In dichloromethane at 20℃; | 100% |
potassium-exchanged zirconium hydrogen phosphate In dichloromethane for 1h; Heating; | 86% |
With 18-crown-6 ether; zinc(II) iodide |
Conditions | Yield |
---|---|
With ammonium chloride; zinc In tetrahydrofuran for 19h; Barbier-type allylation reaction; | 100% |
N-(tert-butyl)-N-(1-chloro-1,1-dimethylsilyl)amine
2-indanone
N-(tert-butyl)-N-(1-(1H-2-indenyloxy)-1,1-dimethylsilyl)amine
Conditions | Yield |
---|---|
With diisopropylamine In tetrahydrofuran | 99.7% |
6-hydroxy-[1,3]dioxolo[4,5-e]isobenzofuran-8(6H)-on
2-indanone
6-(2-oxo-2,3-dihydro-1H-inden-1-yl)-[1,3]dioxolo[4,5-e]isobenzofuran-8(6H)-one
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene for 5h; Heating; | 99% |
carbon dioxide
2-indanone
methyl iodide
methyl 2-oxo-2,3-dihydro-1H-indane-1-carboxylate
Conditions | Yield |
---|---|
With poly(dimethylsiloxane-co-methylhydrosiloxane)trimethylsilyl terminated supported 1-carboxy-6-ethyl-1,8-diazabicyclo[5.4.0]undec-7-ene In methanol at 25 - 27℃; under 760.051 Torr; for 4h; | 99% |
Conditions | Yield |
---|---|
With trifluoroacetic anhydride In tetrahydrofuran at 100℃; Sealed tube; Inert atmosphere; | 99% |
2-indanone
Sodium; 2-hydroxy-indan-2-sulfonate
Conditions | Yield |
---|---|
With sodium hydrogensulfite In water | 98% |
With benzyl butanoate; sodium hydrogensulfite In methanol; water for 0.00833333h; chemoselective reaction; |
Conditions | Yield |
---|---|
With L-Tartaric acid; 1,1-Dimethylurea at 70℃; for 3h; | 98% |
Conditions | Yield |
---|---|
With ammonium formate; C25H31ClIrN2OP at 50℃; for 18h; Leukardt-Wallach Amination; Sealed tube; | 98% |
With palladium on activated charcoal; hydrogen; acetic acid; benzylamine In isopropyl alcohol at 80℃; under 22502.3 Torr; Solvent; Pressure; Autoclave; | 93% |
Multi-step reaction with 4 steps 1: lithium aluminium tetrahydride / diethyl ether / 2 h / 0 °C / Schlenk technique; Reflux; Inert atmosphere 2: triethylamine / dichloromethane / 0 - 20 °C / Schlenk technique; Inert atmosphere 3: sodium azide / N,N-dimethyl-formamide / 90 °C / Schlenk technique; Inert atmosphere 4: hydrogen; palladium on carbon / ethyl acetate / 12 h / 750.08 Torr / Schlenk technique View Scheme |
Conditions | Yield |
---|---|
With acetic acid for 0.333333h; | 97.6% |
With acetic acid In ethanol for 24h; |
2-methoxyacetonitrile
2-indanone
(Z)-1-(1'-amino-2'-methoxy)ethylidene-2-indanone
Conditions | Yield |
---|---|
With heptahydridobis(triphenylphosphine)rhenium In tetrahydrofuran at 150℃; for 5h; Inert atmosphere; teflon-cocked sealed tube; | 97% |
anthranilic acid amide
2-indanone
1,3-dihydro-1'H-spiro[indene-2,2'-quinazolin]-4'(3'H)-one
Conditions | Yield |
---|---|
With Amberlyst-15 In acetonitrile at 20℃; for 0.0333333h; Irradiation; Green chemistry; | 97% |
2-amino-5-iodoanthranilamide
2-indanone
6'-iodo-1,3-dihydro-1'H-spiro[indene-2,2'-quinazolin]-4'(3'H)-one
Conditions | Yield |
---|---|
With Amberlyst-15 In acetonitrile at 20℃; for 0.0333333h; Irradiation; Green chemistry; | 97% |
4-methoxyphenylhydrazine hydrochloride
2-indanone
5,6-dihydro-9-methoxyindeno<2,1-b>indole
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In water; isopropyl alcohol | 96.7% |
With hydrogenchloride In ethanol for 2h; Heating; | 50% |
2-indanone
6-amino-3,4-benzodioxane
N-2,3-Dihydro-benzo[1,4]dioxin-6-yl-N-indan-2-ylamine
Conditions | Yield |
---|---|
Stage #1: 2-indanone; 6-amino-3,4-benzodioxane With sodium tris(acetoxy)borohydride; acetic acid In 1,2-dichloro-ethane at 0 - 20℃; Stage #2: With sodium hydroxide In ethyl acetate; 1,2-dichloro-ethane | 96.5% |
With sodium tris(acetoxy)borohydride; acetic acid In 1,2-dichloro-ethane at 0 - 20℃; | 96.5% |
Conditions | Yield |
---|---|
With heptahydridobis(triphenylphosphine)rhenium In tetrahydrofuran at 150℃; for 5h; Inert atmosphere; teflon-cocked sealed tube; | 96% |
2-amino-benzenethiol
2-indanone
2,3-Dihydro-1,3-benzothiazole<2-spiro-2'>indane
Conditions | Yield |
---|---|
In methanol for 0.333333h; Heating; | 95% |
Nonafluorobutanesulfonyl fluoride
2-indanone
1H-inden-2-yl nonafluorobutanesulfonate
Conditions | Yield |
---|---|
With tert-butylimino-tri(pyrrolidino)phosphorane In tetrahydrofuran at 20℃; for 16h; | 95% |
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol; water at 20℃; for 3h; | 94% |
toluene-4-sulfonic acid hydrazide
2-indanone
2-Indanon-p-tolylsulfonylhydrazon
Conditions | Yield |
---|---|
In ethanol for 3h; Heating; | 93% |
Conditions | Yield |
---|---|
With copper(II) bis(trifluoromethanesulfonate) In dichloromethane at 20℃; for 12h; | 93% |
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