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Cas:13304-62-6
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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
DayangChem exported this product to many countries and regions at best price in China. If you are looking for the product’s supplier in China, DayangChem is your best choice. As a leading manufacturer and supplier of chemicals in China, Day
Cas:13304-62-6
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Cas:13304-62-6
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inquiryOur Advantage Rich Experience Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. Quality service Company cooperates with research institutes. We strictly con
Cas:13304-62-6
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Cas:13304-62-6
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Cas:13304-62-6
Min.Order:1 Kilogram
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inquiryN-Benzylacrylamide CAS:13304-62-6 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 inter
Cas:13304-62-6
Min.Order:1 Gram
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Type:Lab/Research institutions
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Cas:13304-62-6
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Reliable quality 13304-62-6 Best price N-Benzylacrylamide manufacturer Molecular Formula C10H11NO Molar Mass 161.21 Density 1.031g/cm3 Melting Point 59-62°C Boling Point 349.6°C at
Cas:13304-62-6
Min.Order:1 Gram
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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:13304-62-6
Min.Order:10 Gram
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inquiryProduct name: N-Benzylacrylamide CAS No.:13304-62-6 Molecule Formula:C10H11NO Molecule Weight:161.20 Purity: 98.0% Package: 25kg/drum Description:White or off-white powder Manufacture Standards:Enterprise Standard
Cas:13304-62-6
Min.Order:1 Kilogram
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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
Cas:13304-62-6
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inquiry1.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
Cas:13304-62-6
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inquiryHigh 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
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Cas:13304-62-6
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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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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
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 2h; | 99% |
Conditions | Yield |
---|---|
With copper(ll) bromide In tetrahydrofuran at 20℃; for 0.00294444h; Inert atmosphere; Flow reactor; | 99% |
Conditions | Yield |
---|---|
With potassium carbonate In water; acetone at 0℃; for 1h; Inert atmosphere; | 98% |
With triethylamine In dichloromethane at 0 - 20℃; for 12h; | 97% |
With potassium carbonate In water; acetone at 0℃; for 2.5h; | 96% |
Conditions | Yield |
---|---|
A n/a B 98% | |
A n/a B 98% |
Conditions | Yield |
---|---|
With sulfuric acid at 50℃; for 3h; | 96.4% |
With phosphorus pentoxide; silica gel at 90℃; for 3h; Ritter reaction; | 90% |
With sulfuric acid at 10 - 60℃; | 86.8% |
HY zeolite exchanged using rare earth chloride mixture at 100℃; for 24h; Addition; | 61% |
With sulfuric acid |
Conditions | Yield |
---|---|
at 70℃; for 16h; | 96% |
acrylonitrile
benzyl alcohol
A
benzylacrylate
B
N-benzylacrylamide
Conditions | Yield |
---|---|
Stage #1: acrylonitrile; benzyl alcohol With trimethylsilyl trifluoromethanesulfonate at 20℃; for 65h; Pinner Imino Ether Synthesis; Stage #2: With water | A 4% B 90% |
Conditions | Yield |
---|---|
Multistep reaction; | 89% |
2-chloropropionyl chloride
benzylamine
A
chloropropionic acid
B
N-benzylacrylamide
C
Beclamide
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 100℃; for 0.0833333h; Temperature; Concentration; | A 6% B 5% C 89% |
Conditions | Yield |
---|---|
at 70℃; for 16h; | 76% |
Beclamide
N-benzylacrylamide
Conditions | Yield |
---|---|
With sodium hydride In hexane; N,N-dimethyl-formamide; mineral oil at 20℃; for 24h; | 75% |
With potassium hydroxide |
N-benzyl 3-methylthiopropionamide
N-benzylacrylamide
Conditions | Yield |
---|---|
With Selectfluor In 1,4-dioxane at 110℃; for 12h; Schlenk technique; Sealed tube; | 72% |
Conditions | Yield |
---|---|
Stage #1: acrylic acid With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0℃; for 0.25h; Inert atmosphere; Stage #2: benzylamine With triethylamine In dichloromethane at 0 - 20℃; for 8h; Inert atmosphere; | 70% |
With fluorosulfonyl fluoride; N-ethyl-N,N-diisopropylamine In acetonitrile at 20℃; for 5h; | 57% |
With 2-nitrophenyl thiocyanate; tributylphosphine In tetrahydrofuran | |
With thionyl chloride Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
With sodium hydroxide | 70% |
Conditions | Yield |
---|---|
With oxygen; sodium hydroxide In tetrahydrofuran; water at 25℃; for 12h; | 60% |
With oxygen; sodium hydroxide In tetrahydrofuran; water at 25℃; for 12h; Green chemistry; | 60% |
acrylonitrile
benzyl alcohol
A
dibenzyl ether
B
N-benzylacrylamide
Conditions | Yield |
---|---|
With Nafion-H at 120℃; for 24h; Ritter reaction; | A 31 % Chromat. B 56% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 30℃; for 168h; Candida antarctica lipase (CAL); | 53% |
2-Methylthiouracil
β-bromopropionic acid N-benzylamide
A
N-benzylacrylamide
B
4-(N-benzylcarbamoylethoxy)-2-methylthiopyrimidine
Conditions | Yield |
---|---|
With potassium hydroxide In N,N-dimethyl-formamide at 100℃; for 72h; | A 38% B 29% C 23% |
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide In dichloromethane | 30% |
6-methyl-2-methylsulfanyl-3H-pyrimidin-4-one
β-bromopropionic acid N-benzylamide
A
N-benzylacrylamide
B
4-(N-benzylcarbamoylethoxy)-6-methyl-2-methylthiopyrimidine
Conditions | Yield |
---|---|
With potassium hydroxide In N,N-dimethyl-formamide at 100℃; for 72h; | A 2.96 g B 2% C 21% |
Conditions | Yield |
---|---|
With tetracarbonyl nickel; toluene Edukt 4: CO; |
Conditions | Yield |
---|---|
In toluene Heating; Yield given; |
4-(N-benzylcarbamoylethoxy)-2-methylthiopyrimidine
A
2-Methylthiouracil
B
N-benzylacrylamide
Conditions | Yield |
---|---|
With sodium hydride; paraffin In tetrahydrofuran |
4-(N-benzylcarbamoylethoxy)-6-methyl-2-methylthiopyrimidine
A
6-methyl-2-methylsulfanyl-3H-pyrimidin-4-one
B
N-benzylacrylamide
Conditions | Yield |
---|---|
With sodium hydride; paraffin In tetrahydrofuran |
carbon dioxide
β-bromopropionic acid N-benzylamide
A
N-benzylacrylamide
B
3-benzyl-3,4,5,6-tetrahydro-2H-1,3-oxazine-2,4-dione
Conditions | Yield |
---|---|
With oxygen; tetraethylammonium perchlorate In N,N-dimethyl-formamide Ambient temperature; | A 40 % Chromat. B 43 % Chromat. |
β-bromopropionic acid N-benzylamide
A
N-benzylacrylamide
B
3-benzyl-3,4,5,6-tetrahydro-2H-1,3-oxazine-2,4-dione
Conditions | Yield |
---|---|
With carbon dioxide; oxygen; tetraethylammonium perchlorate In N,N-dimethyl-formamide Ambient temperature; | A 40 % Chromat. B 43 % Chromat. |
N-acryloyloxy-N-benzyl-acrylamide
N-benzylacrylamide
Conditions | Yield |
---|---|
With potassium carbonate |
Conditions | Yield |
---|---|
Multistep reaction; |
N-benzyl hydroxylalmine
N-benzylacrylamide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 79 percent / Et3N 2: K2CO3 View Scheme |
N-benzylacrylamide
N1,N4-dibenzylfumaramide
Conditions | Yield |
---|---|
tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride In dichloromethane for 4h; Heating; | 98% |
N-benzylacrylamide
tert-butyl acetyl(benzyl)carbamate
t-butyl benzyl(5-(benzylamino)-5-oxopentan-2-yl)carbamate
Conditions | Yield |
---|---|
Stage #1: tert-butyl acetyl(benzyl)carbamate With diisobutylaluminium hydride In tetrahydrofuran; hexane at -40℃; for 0.5h; Stage #2: With methanol In tetrahydrofuran; hexane for 0.5h; Stage #3: N-benzylacrylamide With samarium diiodide; boron trifluoride diethyl etherate In tetrahydrofuran; hexane; tert-butyl alcohol at -40℃; for 0.166667h; Michael addition; | 95% |
N-benzylacrylamide
thioacetic acid
S-{3-oxo-3-[(phenylmethyl)amino]propyl}ethanethioate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane for 12h; Michael Addition; Inert atmosphere; Reflux; | 94% |
N-benzylacrylamide
methyl 4-(aminomethyl)benzoate hydrochloride
Conditions | Yield |
---|---|
With triethylamine In methanol for 24h; Reflux; | 92% |
N-benzylacrylamide
phenylacetonitrile
Conditions | Yield |
---|---|
With CoI2(dppe); water; zinc(II) iodide; zinc at 80℃; for 12h; Inert atmosphere; regioselective reaction; | 91% |
Ac-Cys-OMe
N-benzylacrylamide
Conditions | Yield |
---|---|
In water; tert-butyl alcohol at 37℃; pH=7.4; Inert atmosphere; | 91% |
Conditions | Yield |
---|---|
With CoI2(dppe); water; zinc(II) iodide; zinc at 80℃; for 12h; Inert atmosphere; regioselective reaction; | 90% |
difluoromethylsulfonyl chloride
N-benzylacrylamide
Conditions | Yield |
---|---|
With dipotassium hydrogenphosphate; [Cu(2,9-bis(4-methoxyphenyl)-1,10-phenanthroline)2]Cl In 1,2-dichloro-ethane at 100℃; Sealed tube; Inert atmosphere; Irradiation; | 90% |
Conditions | Yield |
---|---|
With C47H62N2O3Ru In tetrahydrofuran at 25℃; for 36h; Alkene (Olefin) Metathesis; Inert atmosphere; Sealed tube; diastereoselective reaction; | 90% |
N-benzylacrylamide
Conditions | Yield |
---|---|
With acetic anhydride; periodic acid; chromium(VI) oxide In acetonitrile at -10℃; | 88% |
N-benzylacrylamide
Conditions | Yield |
---|---|
With trimethylsilyl iodide; 1,1,1,3,3,3-hexamethyl-disilazane In dichloromethane at 20℃; for 2h; Michael reaction; | 86% |
With t-butyldimethylsiyl triflate; triethylamine; tert-butyl alcohol In 1,2-dichloro-ethane at 20℃; for 24h; Michael reaction; |
1-(6,7-dimethoxy-1-phenyl-3,4-dihydroisoquinolin-2(1H)-yl)pent-4-en-1-one
N-benzylacrylamide
Conditions | Yield |
---|---|
With C47H62N2O3Ru In tetrahydrofuran at 25℃; for 40h; Alkene (Olefin) Metathesis; Inert atmosphere; Sealed tube; diastereoselective reaction; | 86% |
propyl cyanide
N-benzylacrylamide
(5E)-1-benzyl-5-propylidenepyrrolidin-2-one
Conditions | Yield |
---|---|
With CoI2(dppe); water; zinc(II) iodide; zinc at 80℃; for 12h; Inert atmosphere; regioselective reaction; | 83% |
4-fluorophenylacetonitrile
N-benzylacrylamide
(5E)-1-benzyl-5-(4-fluorobenzylidene)pyrrolidin-2-one
Conditions | Yield |
---|---|
With CoI2(dppe); water; zinc(II) iodide; zinc at 80℃; for 12h; Inert atmosphere; regioselective reaction; | 83% |
N-benzylacrylamide
2-phenyl-1,3-thiazole-4-carboxylic acid methyl ester
Conditions | Yield |
---|---|
With silver(I) acetate; palladium diacetate In dimethyl sulfoxide; N,N-dimethyl-formamide at 115℃; for 48h; Heck reaction; | 83% |
N-benzylacrylamide
3-iodo-7-methoxy-chromen-4-one
(E)-N-benzyl-3-(7-methoxy-4-oxo-4H-chromen-3-yl)acrylamide
Conditions | Yield |
---|---|
With palladium diacetate; triethylamine In N,N-dimethyl-formamide at 100℃; for 0.116667h; Heck Reaction; Microwave irradiation; | 82% |
With palladium diacetate; triethylamine In N,N-dimethyl-formamide at 80℃; for 0.0833333h; Heck Reaction; Microwave irradiation; Green chemistry; |
naphthalen-1-ylacetonitrile
N-benzylacrylamide
(5E)-1-benzyl-5-(1-naphthylmethylene)pyrrolidin-2-one
Conditions | Yield |
---|---|
With CoI2(dppe); water; zinc(II) iodide; zinc at 80℃; for 12h; Inert atmosphere; regioselective reaction; | 81% |
N-benzylacrylamide
(S)-N-benzyl 2,3-dihydroxypropionamide
Conditions | Yield |
---|---|
With methanesulfonamide; AD-mix-β In water; tert-butyl alcohol at 0℃; for 48h; Sharpless Dihydroxylation; | 80% |
Conditions | Yield |
---|---|
With 1,10-Phenanthroline; 4-tert-Butylcatechol; palladium diacetate; N-fluorobis(benzenesulfon)imide In dichloromethane; water at 20 - 25℃; for 20h; Inert atmosphere; | 80% |
Conditions | Yield |
---|---|
With C47H62N2O3Ru In tetrahydrofuran at 25℃; for 24h; Alkene (Olefin) Metathesis; Inert atmosphere; Sealed tube; diastereoselective reaction; | 80% |
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