Dayangchem's 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. DayangChem can provide different quantities
Cas:1125-70-8
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
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:1125-70-8
Min.Order:1 Kilogram
FOB Price: $139.0 / 210.0
Type:Trading Company
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Cas:1125-70-8
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
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Cas:1125-70-8
Min.Order:0
Negotiable
Type:Lab/Research institutions
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
Cas:1125-70-8
Min.Order:0
Negotiable
Type:Lab/Research institutions
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:1125-70-8
Min.Order:10 Gram
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Type:Lab/Research institutions
inquiryBenzeneacetamide, a-methyl-; 2-Phenylpropanamide CAS No.: 1125-70-8 Molecular formula: C9H11NO Molecular weight: 149.19 Benzeneacetamide, a-methyl- nature Benzeneacetamide, a-methyl- use and synthesis Security Information MSDS inf
Cas:1125-70-8
Min.Order:100 Gram
Negotiable
Type:Lab/Research institutions
inquiryZhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed
Cas:1125-70-8
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
inquiry1.A strong technical force and advanced processing equipments. The quality of the products has been strictly inspected and all kinds of index have reached or exceeded domestic and international standards.2. Now we have established long-term stable re
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:Beijing or Guangzhou
factory?direct?sale Application:healing drugs
Cas:1125-70-8
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryBenzeneacetamide, a-methyl- cas 1125-70-8Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
1,we produce and sell good chemicals around the world. 2,our success rate is about 95%. this means, if customer order is accepted, the probability that the customer will obtain the ordered substances, is 95%. 3,our staff consists of highl
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Good 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
Best quality & Attractive price & Professional service; Trial & Pilot & CommercialHenan Fine Chemicals Co., LTD. is a diversified technology - oriented integrated company, which mainly concentrates on fine chemicals. Our company is committed to becom
1.Fast and safety delivery by well-reputed shipping line;2.we have our own chemical laboratory and factory3.Reasonable price, excellent quality and attentive service.4.prompt reply.we can reply your inquiry within 12 hours.5.sample free(depends on pr
Conditions | Yield |
---|---|
With dichloro( 1,5-cyclooctadiene)platinum(ll); 4,5-dihydro-3H-dinaphtho[2,1-c:1',2'-e]phosphepine-4-oxide; water; silver nitrate In tert-Amyl alcohol at 80℃; for 1h; Catalytic behavior; Reagent/catalyst; Time; chemoselective reaction; | 99% |
With [RuH(tBu-PNP(-))(CO)]; water In tert-butyl alcohol at 20℃; for 24h; | 99% |
With sodium hydroxide; dihydrogen peroxide In methanol; water for 2h; pH=8.0; | 95% |
2-Phenylpropanal
2-phenylpropanamide
Conditions | Yield |
---|---|
With hydroxylamine; copper diacetate In water at 110℃; for 48h; | 99% |
Multi-step reaction with 2 steps 1: triethylamine / tetrahydrofuran; acetonitrile / 0.17 h / 0 °C 2: lithium aluminium tetrahydride / tetrahydrofuran / 0.17 h / 0 °C View Scheme |
C14H19N3O
2-phenylpropanamide
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 0.166667h; | 97% |
With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 0.166667h; | 97% |
With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 0.166667h; | 97% |
methanol
Benzeneacetamide
A
N-methyl-1-phenyl-1-methylacetamide
B
2-phenylpropanamide
Conditions | Yield |
---|---|
With C54H43ClN3P2Ru(1+)*F6P(1-); caesium carbonate In toluene at 140℃; for 12h; Inert atmosphere; Sealed tube; Green chemistry; | A 8% B 92% |
With C54H43ClN3P2Ru(1+)*F6P(1-); caesium carbonate In toluene at 140℃; for 48h; Inert atmosphere; Sealed tube; Green chemistry; | A 82% B 18% |
Conditions | Yield |
---|---|
90% |
Conditions | Yield |
---|---|
With bis(tri-t-butylphosphine)palladium(0); ammonium chloride In 1-methyl-pyrrolidin-2-one at 120℃; under 22801.5 Torr; for 15h; Catalytic behavior; Time; Reagent/catalyst; regioselective reaction; | 84% |
With bis(tri-t-butylphosphine)palladium(0); ammonium chloride In 1-methyl-pyrrolidin-2-one at 120℃; under 22801.5 Torr; for 24h; Autoclave; | 84% |
Conditions | Yield |
---|---|
With potassium phosphate; tetrakis(triphenylphosphine)nickel(0) In toluene at 60℃; for 16h; | 75% |
Conditions | Yield |
---|---|
With C54H43ClN3P2Ru(1+)*F6P(1-); caesium carbonate In toluene at 140℃; for 6h; Inert atmosphere; Sealed tube; Green chemistry; | 57% |
methyl 2-phenylpropanimidate
2-phenylpropanamide
Conditions | Yield |
---|---|
With aluminum oxide In methanol | 20% |
methanol
methyl hydratropimidate hydrochloride
A
2-phenylpropionic acid methyl ester
C
2-phenylpropanamide
Conditions | Yield |
---|---|
With diethyl ether; ammonia |
Conditions | Yield |
---|---|
With ammonium hydroxide; sulfur | |
With pyridine; ammonium thiosulfate; ammonium polysulfide solution at 190℃; |
2-phenylpropionyl chloride
2-phenylpropanamide
Conditions | Yield |
---|---|
With ammonium hydroxide | |
With ammonia In toluene for 1h; | |
With ammonium hydroxide In water at 10℃; | |
With ammonia In water at 25℃; for 0.5h; | 0.63 g |
Conditions | Yield |
---|---|
With pyridine; ammonium thiosulfate; ammonium polysulfide solution at 190℃; | |
With ammonium hydroxide; sulfur |
1-bromovinylbenzene
potassium cyanide
A
2-phenylacrylonitrile
B
1-phenylethyl cyanide
C
2-phenylpropanamide
Conditions | Yield |
---|---|
With potassium hydroxide; hydrogen In water; benzene at 55℃; for 12h; | A 73 % Chromat. B 23 % Chromat. C 0.05 g |
phenylacetylene
A
styrene
B
ethylbenzene
C
1-phenylethyl cyanide
D
2-phenylpropanamide
Conditions | Yield |
---|---|
With hydrogen; pentacyanocobaltate(II)(3-) In water at 45℃; under 760 Torr; for 24h; / : 2; Yield given. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts; |
phenylacetylene
A
styrene
B
ethylbenzene
C
2-phenylacrylonitrile
D
1-phenylethyl cyanide
E
2-phenylpropanamide
Conditions | Yield |
---|---|
With pentacyanocobaltate(II)(3-); hydrogen In water under 760 Torr; for 24h; Product distribution; Mechanism; different reaction time, other solvent, different reagent ratio (effect of 2,2'-bipyridyl on product distribution); |
formic acid
water
formamide
acetophenone
2-phenylpropanamide
Conditions | Yield |
---|---|
at 125℃; Rate constant; |
phenylacetylene
A
ethylbenzene
B
1-phenylethyl cyanide
C
2-phenylpropanamide
Conditions | Yield |
---|---|
With hydrogen In water at 45℃; under 760 Torr; for 24h; / : 1; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
pyridine
isopropenylbenzene
A
Benzeneacetamide
B
2-phenylpropanamide
Conditions | Yield |
---|---|
at 190℃; |
pyridine
ammonia
isopropenylbenzene
A
Benzeneacetamide
B
2-phenylpropanamide
Conditions | Yield |
---|---|
at 190℃; |
Conditions | Yield |
---|---|
at 240℃; |
Isopropylbenzene
A
benzamide
B
Benzeneacetamide
C
2-phenylpropanamide
Conditions | Yield |
---|---|
at 250 - 260℃; |
phenylacetylene
A
ethylbenzene
B
2-phenylacrylonitrile
C
1-phenylethyl cyanide
D
2-phenylpropanamide
Conditions | Yield |
---|---|
With hydrogen In water at 45℃; under 760 Torr; for 24h; / : 2; Yield given. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts; |
pyridine
1-methyl-1-phenylethyl alcohol
ammonia
A
2-phenylpropanamide
Conditions | Yield |
---|---|
at 190℃; |
2-phenylpropanamide
Conditions | Yield |
---|---|
With ethanol; nickel |
ethanol
(R)-2-phenyl-2-phenylsulfanyl-propionic acid amide
2-phenylpropanamide
styrene
formamide
A
3-phenylpropionamide
B
2-phenylpropanamide
Conditions | Yield |
---|---|
With carbon monoxide; dodecacarbonyl-triangulo-triruthenium In toluene at 180℃; under 7355.76 Torr; for 24h; Product distribution; Further Variations:; Solvents; |
Conditions | Yield |
---|---|
With aluminium trichloride; potassium iodide In water; acetonitrile at 80℃; for 10h; | 92% |
With phosgene In tetrahydrofuran; toluene at 25℃; for 4h; Inert atmosphere; | 82% |
With phosphorus pentoxide; benzene | |
With phosphorus pentachloride |
Conditions | Yield |
---|---|
With tetraethylammonium bromide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In acetonitrile at 20 - 60℃; | 90% |
benzyl alcohol
2-phenylpropanamide
(+/-)-N-benzyl-2-phenylpropanamide
Conditions | Yield |
---|---|
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; caesium carbonate In toluene at 140℃; for 6h; | 81% |
With potassium tert-butylate In toluene at 130℃; for 12h; Inert atmosphere; Schlenk technique; | 182 mg |
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; caesium carbonate In toluene at 130℃; for 3h; Microwave irradiation; |
2-phenylpropanamide
bis(2-phenylpropyl)amine
Conditions | Yield |
---|---|
With [RuCl2(mesitylene)]2; phenylsilane In neat (no solvent) at 100℃; for 5h; Inert atmosphere; chemoselective reaction; | 78% |
Conditions | Yield |
---|---|
With chloro-trimethyl-silane at 40℃; for 5h; | 71% |
With chloro-trimethyl-silane at 20 - 40℃; for 5h; Inert atmosphere; | 71% |
isopropyl alcohol
2-phenylpropanamide
2-methylphenylacetic acid isopropyl ester
Conditions | Yield |
---|---|
With chloro-trimethyl-silane at 40℃; for 5h; | 69% |
With chloro-trimethyl-silane at 20 - 40℃; for 5h; Inert atmosphere; | 69% |
1-bromo-2-(triisopropylsilyl)acetylene
2-phenylpropanamide
Conditions | Yield |
---|---|
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; silver(I) acetate; sodium acetate; silver(I) triflimide In 1,2-dichloro-ethane at 120℃; under 760.051 Torr; for 12h; Schlenk technique; Inert atmosphere; | 67% |
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; cesium adamantane-1-carboxylate; silver(I) acetate; silver(I) triflimide In acetone at 100℃; for 18h; regioselective reaction; | 53% |
Conditions | Yield |
---|---|
With oxygen; palladium diacetate; trifluoroacetic acid at 100℃; for 36h; regioselective reaction; | 64% |
Conditions | Yield |
---|---|
With oxygen; palladium diacetate; trifluoroacetic acid at 100℃; for 36h; regioselective reaction; | 61% |
2-phenylpropanamide
2-(2-iodophenyl)propionamide
Conditions | Yield |
---|---|
With N-iodo-succinimide; palladium diacetate; trifluoroacetic acid In 1,2-dichloro-ethane at 50℃; for 24h; Sealed tube; regioselective reaction; | 58% |
Conditions | Yield |
---|---|
Stage #1: 2-phenylpropanamide With oxygen; sodium bis(2-methoxyethoxy)aluminium dihydride In tetrahydrofuran; toluene at 0 - 25℃; under 760.051 Torr; for 3h; Stage #2: oxalic acid In methanol; diethyl ether | A 47% B 32% |
Conditions | Yield |
---|---|
With oxygen; palladium diacetate; trifluoroacetic acid at 100℃; for 36h; regioselective reaction; | 45% |
2-phenylpropanamide
(R)-2-phenylpropionic acid amide
Conditions | Yield |
---|---|
With potassium phosphate buffer; Rhodococcus sp. AJ270 at 30℃; for 8h; pH=7.0; kinetic resolution; | 44% |
Conditions | Yield |
---|---|
With oxygen; palladium diacetate; acetic acid at 100℃; for 36h; regioselective reaction; | 42% |
2-phenylpropanamide
A
1,2-diphenylpropan-1-one
B
1-phenylethyl cyanide
Conditions | Yield |
---|---|
With diethyl ether Erhitzen des vom Aether befreiten Reaktionsgemisches in Toluol; |
para-methylphenylmagnesium bromide
2-phenylpropanamide
rac-1-(4-methylphenyl)-2-phenylpropan-1-one
Conditions | Yield |
---|---|
With toluene Erhitzen des Reaktionsprodukts mit wss. HCl; | |
With xylene Erhitzen des Reaktionsprodukts mit wss. HCl; |
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