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Cas:5586-73-2
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Cas:5586-73-2
Min.Order:1000 Gram
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inquiryProduct Name: 3,3-Diphenylpropylamine Synonyms: RARECHEM AL BW 0746;TIMTEC-BB SBB000517;LABOTEST-BB LT00053092;ALPHA-(2-AMINOETHYL)DIPHENYLMETHANE;1-AMINO-3,3-DIPHENYL PROPANE;3,3-DIPHENYLPROPYLAMINE;3,3-Diphenyl-1-propanamine;Benzenep
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inquiryProduct Name: 3,3-Diphenylpropylamine Synonyms: 3,3-Diphenylpropylamine 97%;3,3-DIPHENYLPROPYLAMINE 98+% (INTERMEDIATE FOR DIPINE SERIES);3,3'-Diphenylpropylamine ,98%;(2-Aminoethyl)diphenylmethane;3,3-Diphenylpropane-1-amine;γ-Phenylb
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Cas:5586-73-2
Min.Order:1 Gram
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Cas:5586-73-2
Min.Order:1 Gram
FOB Price: $2.0
Type:Lab/Research institutions
inquiry3,3-Diphenylpropylamine Basic information Product Name: 3,3-Diphenylpropylamine Synonyms: RARECHEM AL BW 0746;TIMTEC-BB SBB000517;LABOTEST-BB LT00053092;ALPHA-(2-AMINOETHYL)DIPHENYLMETHANE;1-AMINO-3,3-DIPHENYL PROPANE;3,3-DIPHENYLPROPYLAMINE;3,3-Dip
Cas:5586-73-2
Min.Order:1 Gram
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Type:Lab/Research institutions
inquiryfactory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
Cas:5586-73-2
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Cas:5586-73-2
Min.Order:1 Gram
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Type:Lab/Research institutions
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Cas:5586-73-2
Min.Order:1 Metric Ton
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Type:Trading Company
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We are a Union of chemistry in China, consists of chemists,engineers, laboratories,factories in China. We organize surplus capacity of R&D and production as well as custom synthesis for chemical products and chemical business project. We are supp
Cas:5586-73-2
Min.Order:1 Metric Ton
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Type:Trading Company
inquiry1, High quality with competitive price:2, Fast and safe delivery3.Excellent pre-sales and after-sales service4. Well-trained and professional technologist and sales with rich experience in the field for 5-10 yearsAppearance:see detailed specification
high 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,Pharmaceutical intermediates Transportation:air,sea,courier
R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
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high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
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
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Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether at 35℃; for 4h; | 86% |
With sulfuric acid; acetic acid; platinum Hydrogenation; |
Conditions | Yield |
---|---|
With ammonia; hydrogen In tert-butyl alcohol at 120℃; for 15h; | 86% |
Conditions | Yield |
---|---|
With sulfuric acid; acetic acid; platinum Hydrogenation; | |
With sodium hydroxide; ammonia; hydrogen; nickel In methanol | |
Multi-step reaction with 2 steps 1: amalgamated aluminium 2: platinum; acetic acid; H2SO4 / Hydrogenation View Scheme |
3,3-diphenyl-propionitrile
A
3-diphenylpropyl amine
B
bis-(3,3-diphenyl-propyl)-amine
Conditions | Yield |
---|---|
With ethanol; ammonia; nickel at 100℃; under 117681 Torr; Hydrogenation; | |
With ethanol; nickel at 100℃; under 117681 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether |
Conditions | Yield |
---|---|
With sulfuric acid; acetic acid; platinum Hydrogenation; | |
Multi-step reaction with 3 steps 1: P2O5; benzene 2: amalgamated aluminium 3: platinum; acetic acid; H2SO4 / Hydrogenation View Scheme | |
Multi-step reaction with 2 steps 1: P2O5; benzene 2: platinum; acetic acid; H2SO4 / Hydrogenation View Scheme | |
Multi-step reaction with 2 steps 1: POCl3 / benzene 2: H2, NH3, NaOH / Raney-Ni / methanol View Scheme |
3,3-Diphenyl-1-benzenesulfonamidopropane
3-diphenylpropyl amine
Conditions | Yield |
---|---|
With hydrogenchloride |
Conditions | Yield |
---|---|
With diethyl ether beim Erhitzen des Reaktionsprodukts mit Polyphosphorsaeure und anschliessenden Hydrieren an Palladium in Methanol; |
3,3-diphenyl-allylamine; hydrochloride
3-diphenylpropyl amine
Conditions | Yield |
---|---|
With ethanol; palladium Hydrogenation; |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: sodium amide; diethyl ether 2: P2O5; benzene 3: amalgamated aluminium 4: platinum; acetic acid; H2SO4 / Hydrogenation View Scheme | |
Multi-step reaction with 3 steps 1: sodium amide; diethyl ether 2: P2O5; benzene 3: platinum; acetic acid; H2SO4 / Hydrogenation View Scheme | |
Multi-step reaction with 2 steps 1: sodium amide; diethyl ether 2: platinum; acetic acid; H2SO4 / Hydrogenation View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: AlCl3 2: aqueous HCl View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: AlCl3 2: aqueous HCl View Scheme | |
Multi-step reaction with 2 steps 1: trifluorormethanesulfonic acid / 1 h / 20 °C 2: lithium aluminium tetrahydride / diethyl ether / 4 h / 35 °C View Scheme |
benzyl bromide
A
Ethyl 4[N-benzyl-N(3,3-diphenylpropyl)amino]-1-piperidinecarboxylate
B
3-diphenylpropyl amine
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: trifluorormethanesulfonic acid / 1 h / 20 °C 2: lithium aluminium tetrahydride / diethyl ether / 4 h / 35 °C View Scheme |
(E/Z)-3-(4-methylphenyl)propenenitrile
3-diphenylpropyl amine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: aluminum tri-bromide / 1 h / 20 °C 2: lithium aluminium tetrahydride / diethyl ether / 4 h / 35 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: palladium diacetate; triphenylphosphine; potassium carbonate / N,N-dimethyl-formamide / 125 - 127 °C / Inert atmosphere 2: aluminum tri-bromide / 1 h / 20 °C 3: lithium aluminium tetrahydride / diethyl ether / 4 h / 35 °C View Scheme |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0℃; for 0.75h; | 100% |
With triethylamine In dichloromethane at 0 - 25℃; for 20h; Inert atmosphere; | 84% |
With TEA In chloroform for 18h; Ambient temperature; | |
With triethylamine In tetrahydrofuran at 0℃; for 2h; |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
In tetrahydrofuran for 0.5h; Ambient temperature; | 98% |
3-diphenylpropyl amine
2-Nitrobenzenesulfonyl chloride
N-(3,3-diphenylpropyl)-2-nitrobenzenesulfonamide
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0 - 20℃; | 98% |
3-diphenylpropyl amine
diisopropylamine
N-isopropyl-3,3-diphenylpropan-1-amine
Conditions | Yield |
---|---|
With μ-diiodo-di((η5-pentamethylcyclopentadienyl)(iodo)iridium) In 5,5-dimethyl-1,3-cyclohexadiene at 155℃; for 10h; Inert atmosphere; | 98% |
BOC-glycine
3-diphenylpropyl amine
[(3,3-diphenyl-propylcarbamoyl)-methyl]-carbamic acid tert-butyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 16h; Inert atmosphere; | 97% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 16h; | 90% |
3-diphenylpropyl amine
N-(4-isothiocyanatomethylphenyl)methanesulfonamide
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 96% |
3-diphenylpropyl amine
2-(4-hydroxyphenyl)-2-phenylacetic acid
N-(3,3-diphenylpropyl)-2-(4-hydroxyphenyl)-2-phenylacetamide
Conditions | Yield |
---|---|
With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; for 12h; Schlenk technique; Inert atmosphere; | 95% |
With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; for 4h; | 71% |
3-diphenylpropyl amine
dimethyl N-cyanodithioiminocarbonate
N-cyano-N'-(3,3-diphenylpropyl)-S-methylisothiourea
Conditions | Yield |
---|---|
In dichloromethane for 0.5h; | 94% |
3-diphenylpropyl amine
Conditions | Yield |
---|---|
With dicyclohexyl-(2′,4′,6′-triisopropyl-3,6-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine; palladium diacetate; lithium tert-butoxide In toluene at 95℃; for 16h; Schlenk technique; Inert atmosphere; diastereoselective reaction; | 94% |
Conditions | Yield |
---|---|
With triethylamine In chloroform for 1h; Reflux; Inert atmosphere; | 94% |
3-diphenylpropyl amine
(3aRS,7aRS)-7a-(3-bromopropyl)-3a,4,7,7a-tetrahydroisobenzofuranone
Conditions | Yield |
---|---|
In toluene for 16h; Heating; | 93% |
Conditions | Yield |
---|---|
With 4-methyl-morpholine; benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 20℃; | 93% |
Conditions | Yield |
---|---|
In ethanol Heating; | 92% |
5-[2-[(4-biphenylylcarbonyl)amino]ethyl]-1,2,4-oxadiazole-3-carboxylic acid ethyl ester
3-diphenylpropyl amine
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In acetonitrile for 24h; Heating / reflux; | 92% |
formaldehyd
trimethylsilylazide
3-diphenylpropyl amine
1,1,3,3-tetramethylbutane isonitrile
(3,3-diphenylpropyl)-[(1-(1,1,3,3-tetramethylbutyl)-1H-tetrazol-5-yl)methyl]amine
Conditions | Yield |
---|---|
In methanol at 80℃; for 1.5h; Ugi condensation; Inert atmosphere; Microwave irradiation; Sealed tube; | 92% |
3-diphenylpropyl amine
Conditions | Yield |
---|---|
Stage #1: 3-diphenylpropyl amine With sodium carbonate In dichloromethane at 25℃; for 0.0166667h; Stage #2: (4-fluorophenyl)(3,3,3-trifluoroprop-1-en-2-yl)iodonium trifluoromethane sulfonate In dichloromethane at 25℃; for 2.5h; | 92% |
3-diphenylpropyl amine
N-cyanodiphenylcarbonimidate
1-cyano-3-(3,3-diphenylpropyl)-2-phenylisourea
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 1h; | 91% |
Conditions | Yield |
---|---|
Stage #1: 3-diphenylpropyl amine; acetone With sodium tris(acetoxy)borohydride; acetic acid In 1,2-dichloro-ethane at 20℃; for 0.0833333h; Stage #2: In tetrahydrofuran; 1,2-dichloro-ethane at 20℃; for 3h; | 90.9% |
Conditions | Yield |
---|---|
90% |
3-diphenylpropyl amine
1,3-Bis(3,3-diphenylpropyl)harnstoff
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide | 90% |
(1S,3R,4S,5R)-3,4-O-isopropylidene-1,5-quinic lactone
3-diphenylpropyl amine
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 60℃; for 0.0833333h; Microwave irradiation; | 90% |
Conditions | Yield |
---|---|
With 1,3-dimethylbenzimidazolium-2-carboxylate; phenylsilane In acetonitrile at 25℃; under 750.075 Torr; for 24h; Catalytic behavior; | 90% |
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide | 89.5% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; | 88% |
3-diphenylpropyl amine
2-hydroxy-2-phenylbutanoic acid
Conditions | Yield |
---|---|
Stage #1: 2-hydroxy-2-phenylbutanoic acid With 1,1'-carbonyldiimidazole In dichloromethane at 20℃; for 1.5h; Stage #2: 3-diphenylpropyl amine In dichloromethane at 20℃; for 10h; | 89% |
3-diphenylpropyl amine
3-ethoxy-4,5,6,7-tetrahydro-1,2-benzisoxazol-4-one
Conditions | Yield |
---|---|
With 3 A molecular sieve; sodium cyanoborohydride In methanol at 20℃; for 16h; | 89% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 60℃; for 0.0833333h; Microwave irradiation; | 88% |
3-diphenylpropyl amine
2-hydroxy-2-phenyl-heptanoic acid
Conditions | Yield |
---|---|
Stage #1: 2-hydroxy-2-phenyl-heptanoic acid With 1,1'-carbonyldiimidazole In dichloromethane at 20℃; for 1.5h; Stage #2: 3-diphenylpropyl amine In dichloromethane at 20℃; for 10h; | 87% |
3-diphenylpropyl amine
3-(anthracen-9-yl)-2-hydroxybenzaldehyde
Conditions | Yield |
---|---|
With formic acid In ethanol | 87% |
Conditions | Yield |
---|---|
In ethanol Heating; | 87% |
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