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
Carbonicacid,di-2-propen-1-ylester Molecular weight:142 Formula:: C7H10O3 CAS :15022-08-9 Description: Diallyl Carbonate is colorless liquid with irritant odor Boiling point: 95-97℃@ 60 mm Hg,(172.3℃ @760mmHg) Chemical Properties &
Cas:15022-08-9
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inquiryDIALLYL CARBONATE CAS:15022-08-9 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 interm
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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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inquiryZibo 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:15022-08-9
Min.Order:10 Gram
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inquiryDIALLYL CARBONATE Basic information Product Name: DIALLYL CARBONATE Synonyms: Allyl carbonate;Carbonic acid, di-2-propenyl ester;Carbonic acid, diallyl ester;ca
Cas:15022-08-9
Min.Order:1 Metric Ton
Negotiable
Type:Lab/Research institutions
inquiryProduct name: Diallyl Carbonate CAS No.:15022-08-9 Molecule Formula:C7H10O3 Molecule Weight:142.15 Purity: 99.0% Package: 200kg/drum Description:Colorless liquid Manufacture Standards:Enterprise Standard TESTING ITEMS
Cas:15022-08-9
Min.Order:1 Kilogram
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inquiryMolecular weight:144 Formula:: C7H10O3 CAS :15022-08-9 Description: Diallyl Carbonate is colorless liquid with irritant odor Boiling point: 95-97℃@ 60 mm Hg,(172.3℃ @760mmHg); APplication:Raw material to produce Diethylene Glycol Bis-allyl
R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
Cas:15022-08-9
Min.Order:0
Negotiable
Type:Manufacturers
inquiryhigh 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:Beijing or Guangzhou
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
Cas:15022-08-9
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inquiryCarbonic acid,di-2-propen-1-yl ester cas 15022-08-9Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
Cas:15022-08-9
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inquiryfactory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Stock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
The factory supplies Application:manufacturing supplies
Cas:15022-08-9
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inquiryGood Quality Package:1kg/bag Application:Medical or chemical Transportation:Air/Train/Sea Port:Shenzhen
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Price, service, company and transport advantage: 1. Best service, place of origin China, high quality, and reasonable price. 2. It's customers' right to choose the package (EMS, DHL, FEDEX, UPS). 3. It's customers' right
Cas:15022-08-9
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inquiryJoyinchem have been committed to chemical supply for several years and have built good cooperation records with multinational chemical corporations and importers from all over the world. Our services include:-Spot goods-Contract manufacturing-Custom
Cas:15022-08-9
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inquiryFINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the DIALLYL CARBONATE, CAS:15022-08-9 with the most competitive price and the best qualit
Diallyl carbonate 15022-08-9 Pharma Grade For Human HealthAppearance:White to almost white crystalline powder Storage:Store in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/Pharmaceutical intermedi
Cas:15022-08-9
Min.Order:0
Negotiable
Type:Trading Company
inquiryConditions | Yield |
---|---|
With 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine In neat (no solvent) at 80℃; under 760.051 Torr; for 16h; Inert atmosphere; Green chemistry; | 95% |
With 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine at 80 - 120℃; for 48h; | 61% |
With potassium carbonate at 70℃; for 6h; | 53% |
With sodium methylate at 60℃; for 1h; Inert atmosphere; | 2 %Chromat. |
Conditions | Yield |
---|---|
With copper (I) iodide; dicyclohexyl-carbodiimide at 64.85℃; under 37503 Torr; for 4h; | A 6% B 93% |
With dicyclohexyl-carbodiimide In toluene at 64.85℃; under 37503 Torr; for 6h; | A n/a B 3.3% |
carbon dioxide
allyl alcohol
O-allyl-N,N'-dicyclohexyl isourea
A
Allyl ether
B
diallylcarbonate
Conditions | Yield |
---|---|
at 64.85℃; under 37503 Torr; for 2h; | A 7% B 91% |
Conditions | Yield |
---|---|
With pyridine In diethyl ether a) 0 deg C, 1 h, b) 25 deg C, 5 h; | 85% |
With pyridine In diethyl ether at 25℃; for 5h; | 67% |
Conditions | Yield |
---|---|
With 2-Cyanopyridine; cerium(IV) oxide at 119.84℃; under 37503.8 Torr; for 48h; Autoclave; | 76% |
With dichloromethane; caesium carbonate In 1-methyl-pyrrolidin-2-one at 100℃; under 760.051 Torr; for 24h; | 58% |
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran for 18h; | 40% |
With carbon tetrabromide; tributylphosphine; 2-cyclohexyl-1,1,3,3-tetramethylguanidine In N,N-dimethyl-formamide at 20℃; for 2h; Condensation; | 64.1 % Spectr. |
allyl alcohol
diallylcarbonate
Conditions | Yield |
---|---|
With lanthanum(III) chloride; urea at 180℃; for 6h; Reagent/catalyst; Autoclave; | 60.7% |
potassium hydrogencarbonate
allyl bromide
A
Allyl ether
B
diallylcarbonate
Conditions | Yield |
---|---|
tetrabutyl phosphonium bromide In various solvent(s) at 150℃; Solvent: NMP; | A n/a B 50% |
allyl alcohol
carbonic acid dimethyl ester
A
allyl methyl carbonate
B
diallylcarbonate
Conditions | Yield |
---|---|
Stage #1: allyl alcohol; carbonic acid dimethyl ester at 80℃; Stage #2: With 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine at 80℃; for 1h; | A 50% B n/a |
sodium methylate at 23℃; Inert atmosphere of nitrogen; | |
sodium methylate at 23℃; Inert atmosphere of nitrogen; | |
With sodium aluminate at 20 - 90℃; for 24h; |
(2-oxo-1,3-dioxolan-4-yl)methyl 4-methylbenzenesulfonate
allyl alcohol
A
diallylcarbonate
B
allyl glycidyl carbonate
Conditions | Yield |
---|---|
Stage #1: allyl alcohol With sodium hydride In tetrahydrofuran Stage #2: (2-oxo-1,3-dioxolan-4-yl)methyl 4-methylbenzenesulfonate With tetrabutylammomium bromide In tetrahydrofuran at -70 - 20℃; | A 12% B 47% |
tri-n-propylamine
carbon dioxide
A
diallylcarbonate
B
propyl N,N-di-propylcarbamate
Conditions | Yield |
---|---|
With allyl alcohol; acetylene at 160℃; for 16h; | A 6% B 4% C 21% |
tri-n-propylamine
carbon dioxide
allyl alcohol
A
diallylcarbonate
B
propyl N,N-di-propylcarbamate
Conditions | Yield |
---|---|
With acetylene at 160℃; for 16h; | A 6% B 4% C 21% |
carbon dioxide
triethylamine
allyl alcohol
A
diallylcarbonate
B
ethyl N,N-diethylcarbamate
C
allyl ethyl carbonate
Conditions | Yield |
---|---|
With acetylene at 160℃; for 16h; | A 8% B 14% C 19% |
carbon dioxide
allyl alcohol
A
diallylcarbonate
B
ethyl N,N-diethylcarbamate
C
allyl ethyl carbonate
Conditions | Yield |
---|---|
With triethylamine; acetylene at 160℃; for 16h; | A 8% B 14% C 19% |
phosgene
allyl alcohol
A
diallylcarbonate
B
Allyl chloroformate
Conditions | Yield |
---|---|
With ethanol; sodium ethanolate | |
With sodium |
diallyl oxalate
A
diallylcarbonate
carbon dioxide
allyl alcohol
N,N'-dicyclohexyl-O-methyl isourea
A
allyl methyl carbonate
B
diallylcarbonate
Conditions | Yield |
---|---|
In acetonitrile at 59.85℃; |
diallylcarbonate
Conditions | Yield |
---|---|
In dimethylsulfoxide-d6 at 100℃; under 15201 Torr; for 24h; Pressure; Inert atmosphere; | 73 %Spectr. |
carbon dioxide
N,N-Dimethylformamide diallyl acetal
N,N-dimethylformamide dibenzyl acetal
A
diallylcarbonate
B
DBC
C
O-Alloc benzyl alcohol
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 100℃; under 760.051 Torr; for 24h; Inert atmosphere; Overall yield = 44 %; |
Conditions | Yield |
---|---|
With sodium methylate at 60℃; for 1h; Inert atmosphere; | 2 %Chromat. |
Conditions | Yield |
---|---|
With sodium methylate In neat (no solvent) at 60℃; for 1h; Catalytic behavior; Temperature; Reagent/catalyst; Inert atmosphere; | 73 %Chromat. |
1,3-benzodioxol-2-one
allyl alcohol
A
diallylcarbonate
B
benzene-1,2-diol
Conditions | Yield |
---|---|
With sodium methylate at 60℃; for 1h; Reagent/catalyst; Temperature; Inert atmosphere; | A 73 %Chromat. B n/a |
diallylcarbonate
1'-<(trimethylsilyl)oxy>-2'-methylspiro<1,3-dioxolane-2,4'-cyclohexene>
7-allyl-7-methyl-1,4-dioxaspiro[4.5]decan-8-one
Conditions | Yield |
---|---|
With tetrabutylammonium triphenyldifluorosilicate; tris-(dibenzylideneacetone)dipalladium(0); (S)-4-tert-butyl-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro-1,3-oxazol In tetrahydrofuran at 25℃; for 2h; Product distribution / selectivity; | 99% |
diallylcarbonate
Benzoylformic acid
(E)-1-phenyl-2-buten-1-one
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0); Tri(p-tolyl)phosphine In 1,4-dioxane at 100℃; for 12h; Inert atmosphere; | 99% |
diallylcarbonate
tert-butyl 3-hydroxy-3-(1-methyl-4-nitro-1H-pyrazol-5-yl)propanoate
tert-butyl 3-(allyloxy)-3-(1-methyl-4-nitro-1H-pyrazol-5-yl)propanoate
Conditions | Yield |
---|---|
With tris-(dibenzylideneacetone)dipalladium(0); triphenylphosphine In 1,4-dioxane at 65℃; for 1h; Inert atmosphere; | 99% |
diallylcarbonate
3,4-dihydronaphthalene-1(2H)-one
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran; mineral oil at 20℃; for 12h; | 99% |
Conditions | Yield |
---|---|
With potassium carbonate at 130℃; for 16h; | 98% |
diallylcarbonate
(E)-1-(3-hydroxyphenyl)-2-(3-hydroxyphenyl)ethene
Conditions | Yield |
---|---|
With tetrabutylammomium bromide at 120℃; for 20h; Inert atmosphere; | 98% |
diallylcarbonate
2-([1,1’-biphenyl]-4-yl)-2-oxoacetic acid
(E)-1-([1,1'-biphenyl]-4-yl)but-2-en-1-one
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0); Tri(p-tolyl)phosphine In 1,4-dioxane at 100℃; for 12h; Inert atmosphere; | 97% |
diallylcarbonate
(2-ethylcyclohex-1-enyloxy)trimethylsilane
(+)-2-allyl-2-ethylcyclohexanone
Conditions | Yield |
---|---|
With tetrabutylammonium triphenyldifluorosilicate; tris-(dibenzylideneacetone)dipalladium(0); (S)-4-tert-butyl-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro-1,3-oxazol In tetrahydrofuran at 25℃; for 3h; Product distribution / selectivity; | 96% |
With tris-(dibenzylideneacetone)dipalladium(0); tetrabutylammonium triphenyldifluorosilicate; (S)-4-tert-butyl-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro-1,3-oxazol In tetrahydrofuran at 25℃; for 4h; asymmetric Tsuji allylation; Inert atmosphere; optical yield given as %ee; | 96% |
diallylcarbonate
4,4-ethylenedioxy-piperidine
Conditions | Yield |
---|---|
With 2-hydroxypyridin; zirconium(IV) tert-butoxide at 80℃; for 12h; | 95% |
Conditions | Yield |
---|---|
With 2-hydroxypyridin; zirconium(IV) tert-butoxide at 80℃; for 12h; | 95% |
diallylcarbonate
1-trimethylsilyloxy-2-methyl-1-cyclohexene
(2S)-2-methyl-2-(2-propen-1-yl)cyclohexanone
Conditions | Yield |
---|---|
With tetrabutylammonium triphenyldifluorosilicate; tris-(dibenzylideneacetone)dipalladium(0); (S)-4-tert-butyl-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro-1,3-oxazol In tetrahydrofuran at 25℃; for 2h; Product distribution / selectivity; | 95% |
Conditions | Yield |
---|---|
With NaY at 130℃; for 1.66667h; | 94% |
diallylcarbonate
3,4-dihydronaphthalene-1(2H)-one
allyl 1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate
Conditions | Yield |
---|---|
Stage #1: 3,4-dihydronaphthalene-1(2H)-one With sodium hydride In tetrahydrofuran; mineral oil at 0 - 20℃; for 0.25h; Inert atmosphere; Stage #2: diallylcarbonate In tetrahydrofuran; mineral oil for 16h; Inert atmosphere; | 94% |
With sodium hydride In tetrahydrofuran; mineral oil at 25℃; for 16h; Inert atmosphere; | 93% |
Stage #1: 3,4-dihydronaphthalene-1(2H)-one With sodium hydride In tetrahydrofuran Stage #2: diallylcarbonate In tetrahydrofuran | |
Stage #1: 3,4-dihydronaphthalene-1(2H)-one With sodium hydride In tetrahydrofuran at 0℃; for 0.25h; Stage #2: diallylcarbonate In tetrahydrofuran at 20℃; for 16h; | |
Stage #1: 3,4-dihydronaphthalene-1(2H)-one With sodium hydride In tetrahydrofuran; mineral oil at 0 - 20℃; for 0.25h; Stage #2: diallylcarbonate In tetrahydrofuran; mineral oil at 20℃; for 16h; |
diallylcarbonate
1-<(trimethylsilyl)oxy>-2-methylcycloheptene
Conditions | Yield |
---|---|
With tetrabutylammonium triphenyldifluorosilicate; tris-(dibenzylideneacetone)dipalladium(0); (S)-4-tert-butyl-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro-1,3-oxazol In tetrahydrofuran at 25℃; for 2h; Product distribution / selectivity; | 94% |
diallylcarbonate
1-naphthylglyoxylic acid
(E)-1-(naphthalen-1-yl)but-2-en-1-one
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0); Tri(p-tolyl)phosphine In 1,4-dioxane at 100℃; for 12h; Inert atmosphere; | 94% |
Conditions | Yield |
---|---|
palladium; triphenylphosphine In tetrahydrofuran | 93% |
diallylcarbonate
4-oxo-4,5,6,7-tetrahydrobenzofuran
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran; mineral oil at 25℃; for 16h; Inert atmosphere; | 93% |
diallylcarbonate
Conditions | Yield |
---|---|
Stage #1: diallylcarbonate; O-ethyl S-(2-oxotetrahydrothiophen-3-yl)carbonodithioate In ethyl acetate at 80℃; for 0.25h; Inert atmosphere; Stage #2: With dilauryl peroxide In ethyl acetate for 5h; Inert atmosphere; | 93% |
diallylcarbonate
1-methyl-4-(benzylsulfonyl)benzene
1-Methyl-4-(1-phenyl-but-3-ene-1-sulfonyl)-benzene
Conditions | Yield |
---|---|
With 1,2-bis-(diphenylphosphino)ethane; tris(dibenzylideneacetone)dipalladium(0) chloroform complex In tetrahydrofuran at 65℃; for 3h; | 92% |
With tris(dibenzylideneacetone)dipalladium(0) chloroform complex; 1,2-bis-(diphenylphosphino)ethane In tetrahydrofuran at 65℃; for 1h; | 92% |
(±)-5-methoxy-2-methylindoline
diallylcarbonate
Conditions | Yield |
---|---|
With Candida antarctica lipase B In various solvent(s) at 30℃; for 10h; | A 92% B 88% |
Conditions | Yield |
---|---|
With water at 20℃; for 3h; | 92% |
Conditions | Yield |
---|---|
With sodium hydroxide In 1,4-dioxane; water at 20℃; | 92% |
Conditions | Yield |
---|---|
With 1,2-bis-(diphenylphosphino)ethane; Pd(dibenzylideneacetone)2 chloroform adduct In tetrahydrofuran at 65℃; for 2h; | 91% |
With tris(dibenzylideneacetone)dipalladium(0) chloroform complex; 1,2-bis-(diphenylphosphino)ethane In tetrahydrofuran at 65℃; for 1h; | 91% |
diallylcarbonate
benzeneacetic acid methyl ester
methyl allylphenylacetate
Conditions | Yield |
---|---|
With tris(dibenzylideneacetone)dipalladium(0) chloroform complex; 1,2-bis-(diphenylphosphino)ethane In tetrahydrofuran at 65℃; for 1h; | 91% |
diallylcarbonate
A
benzyl (2R,3aR,7aR)-octahydroindole-2-carboxylate
Conditions | Yield |
---|---|
With IMB-104 Candida antarctica lipase A In various solvent(s) at 30℃; for 72h; | A 90% B 91% |
Conditions | Yield |
---|---|
Stage #1: inden-1-one With sodium hydride In tetrahydrofuran at 0 - 23℃; Inert atmosphere; Stage #2: diallylcarbonate In tetrahydrofuran at 23℃; for 16h; Inert atmosphere; | 91% |
Stage #1: inden-1-one With sodium hydride In tetrahydrofuran; mineral oil at 0 - 20℃; for 0.25h; Stage #2: diallylcarbonate In tetrahydrofuran; mineral oil for 16h; | 62% |
Stage #1: inden-1-one With sodium hydride In tetrahydrofuran at 0℃; for 0.25h; Stage #2: diallylcarbonate In tetrahydrofuran at 20℃; for 16h; | |
Stage #1: inden-1-one With sodium hydride In tetrahydrofuran; mineral oil at 0 - 20℃; for 0.25h; Stage #2: diallylcarbonate In tetrahydrofuran; mineral oil at 20℃; for 16h; |
diallylcarbonate
5-fluoro-3,4-dihydronaphthalen-1(2H)-one
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran; mineral oil at 0 - 20℃; for 21h; | 91% |
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