CAS No.114133-37-8,(s)-3-(methylamino)-1-phenylpropanol (114133-37-8) Suppliers

Dayang Chem (Hangzhou) Co.,Ltd.

DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe

(1S)-3-(Methylamino)-1-phenylpropan-1-ol Manufacturer/High quality/Best price/In stock

Cas:114133-37-8

Min.Order:1 Kilogram

FOB Price: $3.0

Type:Lab/Research institutions

inquiry

Chemwill Asia Co., Ltd.

Our 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

(S)-3-(Methylamino)-1-phenylpropan-1-ol

Cas:114133-37-8

Min.Order:5 Kiloliter

FOB Price: $1.2 / 5.0

Type:Manufacturers

inquiry

Hebei Nengqian Chemical Import and Export Co., LTD

Our 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

(s)-3-(methylamino)-1-phenylpropanol (114133-37-8)

Cas:114133-37-8

Min.Order:1 Kilogram

FOB Price: $9.0 / 99.0

Type:Trading Company

inquiry

Henan Wentao Chemical Product Co., Ltd.

Henan 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

(1S)-3-(Methylamino)-1-phenylpropan-1-ol

Cas:114133-37-8

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

SHANGHAI T&W PHARMACEUTICAL CO., LTD.

A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc

(s)-3-(methylamino)-1-phenylpropanol (114133-37-8)

Cas:114133-37-8

Min.Order:4 Kilogram

Negotiable

Type:Lab/Research institutions

inquiry

Zibo Hangyu Biotechnology Development Co., Ltd

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

(1S)-3-(Methylamino)-1-phenylpropan-1-ol

Cas:114133-37-8

Min.Order:10 Gram

Negotiable

Type:Lab/Research institutions

inquiry

GIHI CHEMICALS CO.,LIMITED

Lower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe

(s)-3-(methylamino)-1-phenylpropanol

Cas:114133-37-8

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Henan Tianfu Chemical Co., Ltd.

(1S)-3-(Methylamino)-1-phenylpropan-1-ol Application:Organic Chemicals

114133-37-8

Cas:114133-37-8

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Antimex Chemical Limied

factory?direct?sale Application:healing drugs

(1S)-3-(Methylamino)-1-phenylpropan-1-ol

Cas:114133-37-8

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

BOC Sciences

We are committed to providing our customers with the best products and services at the most competitive prices.Appearance:crystalline powder Storage:Room temperature with sealed well Package:according to the clients requirement Application:Use as pri

(S)-3-(Methylamino)-1-phenylpropan-1-ol

Cas:114133-37-8

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Hangzhou Fandachem Co.,Ltd

(1S)-3-(Methylamino)-1-phenylpropan-1-ol cas 114133-37-8Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express

(1S)-3-(Methylamino)-1-phenylpropan-1-ol cas 114133-37-8

Cas:114133-37-8

Min.Order:0

Negotiable

Type:Other

inquiry

SAGECHEM LIMITED

laboratory Application:Synthetic building block

Benzenemethanol, a-[2-(methylamino)ethyl]-, (aS)-

Cas:114133-37-8

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Chemlyte Solutions

Stock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai

(s)-3-(methylamino)-1-phenylpropanol (114133-37-8)

Cas:114133-37-8

Min.Order:0

Negotiable

Type:Other

inquiry

ZHEJIANG JIUZHOU CHEM CO.,LTD

factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin

(s)-3-(methylamino)-1-phenylpropanol (114133-37-8)

Cas:114133-37-8

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Amadis Chemical Co., Ltd.

1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G

(S)-3-(Methylamino)-1-phenylpropan-1-ol

Cas:114133-37-8

Min.Order:10 Milligram

Negotiable

Type:Lab/Research institutions

inquiry

ORCHID CHEMICAL SUPPLIES LTD

(1S)-3-(Methylamino)-1-phenylpropan-1-ol

Cas:114133-37-8

Min.Order:0

Negotiable

Type:Other

inquiry

Finetech Industry Limited

High Quality Best Price Storage:Store in dry, dark and ventilated place Application:Chemical Synthesis Intermediate

FT-0771123

Cas:114133-37-8

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Debye Scientific

Debyesci is here who supplied several kinds of chemical products to global pharmaceutical, drug discovery, agrochemical and biotechnology industries for four yearsOur key scientific leadership team has gained experience in top research and developmen

(S)-3-(Methylamino)-1-phenylpropan-1-ol

Cas:114133-37-8

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Langchem

1.We are specializing in providing customers with complete chemical raw materials.2.Superior quality, moderate price & quick delivery.3. Extensive international cooperation experience.4. Outstanding communication skills. Application:contact us for de

(S)-3-(Methylamino)-1-phenylpropan-1ol

Cas:114133-37-8

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Alchemist-pharm chemical Technology Co. Ltd.

R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates

114133-37-8

Cas:114133-37-8

Min.Order:0

Negotiable

Type:Trading Company

inquiry

crucell inc

114133-37-8

(1S)-3-(Methylamino)-1-phenylpropan-1-ol

Cas:114133-37-8

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Synthetic route

: 76183-10-3, 134619-76-4
(S)-3-hydroxy-N-methyl-3-phenylpropanamide

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
With lithium aluminium tetrahydride In diethyl ether	98%
With lithium aluminium tetrahydride In tetrahydrofuran for 2h; Heating;	97.6%
With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 25℃;	90%
With lithium aluminium tetrahydride In tetrahydrofuran for 6h; Reflux;	89%

: 115290-77-2
(1S) 3-phenyl-3-hydroxypropyl methanesulfonate

: 74-89-5
methylamine

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
In tetrahydrofuran; water at 65℃; for 3h;	96%
In tetrahydrofuran; water at 70℃;	93%
In tetrahydrofuran; water at 70℃; for 4h;	90%
In tetrahydrofuran; water at 60 - 65℃; for 4h;	82%

: 2538-50-3
β-Methylaminoethyl phenyl ketone hydrochloride

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
With Rh[((S,S)-BenzP*)(cod)]SbF6; hydrogen; caesium carbonate; zinc(II) chloride In methanol at 20℃; under 19001.3 Torr; for 20h; Autoclave; enantioselective reaction;	92%
With hydrogen; potassium carbonate; [Rh{(SC,RP)-duanphos}(norbornadiene)]SbF6 In methanol at 20℃; under 7500.6 Torr; for 12h;	90%
With [Rh((S,S)-BenzP*)(cod)]SbF6; hydrogen; magnesium sulfate; potassium carbonate In ethyl acetate at 50℃; under 37503.8 Torr; for 1h; enantioselective reaction;	80%

: 27152-62-1
3-(N-methylamino)propiophenone

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
With (S)-(1,1'-binaphthalene)-2,2'-diylbis(diphenylphosphine) In acetonitrile at 20℃; for 5h; Solvent; Reagent/catalyst;	89.93%

: 502697-61-2
(S)-N-(ethoxycarbonyl)-3-amino-1-phenyl-1-propanol

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
With lithium aluminium tetrahydride In tetrahydrofuran for 1h; Heating;	88%

: 114133-36-7
(S)-(-)-3-iodo-1-phenyl-1-propanol

: 74-89-5
methylamine

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
In tetrahydrofuran; water Ambient temperature;	86%
In tetrahydrofuran Ambient temperature;	85%
In tetrahydrofuran; water for 22h;

: 762273-00-7
(S)-(-)-N-(tert-butoxycarbonyl)-3-amino-1-phenylpropan-1-ol

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
With lithium aluminium tetrahydride In tetrahydrofuran for 5.5h; Heating;	78%

: 100306-34-1
3-chloro-1-phenylpropanol

: 74-89-5
methylamine

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
With potassium iodide In methanol; water at 80℃; for 8h;	75%
With sodium iodide In water

: (6S)-2-((S)-1-triisopropylsilyloxyethyl)-3-methyl-6-phenyl-1,3-oxazinane

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
With hydrogenchloride In methanol; water at 90℃; for 1.5h;	67%

: ((S)-3-Hydroxy-3-phenyl-propyl)-carbamic acid methyl ester

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
With lithium aluminium tetrahydride In tetrahydrofuran Heating; Yield given;
With lithium aluminium tetrahydride

: 74-89-5
methylamine

: 51699-49-1
3-hydroxy-3-phenylpropyl 4-methylbenzenesulfonate

A: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

B: 115290-81-8
(R)-N-methyl-3-phenyl-3-hydroxypropylamine

Conditions

Conditions	Yield
Stage #1: 3-hydroxy-3-phenylpropyl 4-methylbenzenesulfonate With 3 A molecular sieve; oxygen; (-)-sparteine; palladium diacetate In toluene at 80℃; under 760 Torr; for 36h; Stage #2: methylamine With water In tetrahydrofuran at 65℃;

...Expand

: N-(3-hydroxy-3-phenyl-propyl)-formamide

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
With lithium aluminium tetrahydride In tetrahydrofuran for 8h; Heating;	4.10 g

: 33401-74-0
ethyl (3R)-3-hydroxy-3-phenylpropionate

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 70 percent / tetrahydrofuran; H2O / 70 °C 2: 90 percent / LiAlH4 / tetrahydrofuran / 0 - 25 °C View Scheme
Multi-step reaction with 4 steps 1: 80 percent / LiAlH4 / diethyl ether / Ambient temperature 2: 85 percent / Et3N / diethyl ether / 2 h / 0 °C 3: 90 percent / NaI / acetone / Heating 4: 86 percent / tetrahydrofuran; H2O / Ambient temperature View Scheme
Multi-step reaction with 3 steps 1: 80 percent / LiAlH4 / diethyl ether / Ambient temperature 2: 85 percent / Et3N / diethyl ether / 2 h / 0 °C 3: 90 percent / tetrahydrofuran; H2O / 4 h / 70 °C View Scheme

: 132203-26-0
(S)-3-hydroxy-3-phenylpropanenitrile

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 92 percent / borane-dimethyl sulfide complex / tetrahydrofuran / 4 h / 70 °C 2: aq. K2CO3 / CH2Cl2 / 0.5 h / 20 °C 3: 4.10 g / LiAlH4 / tetrahydrofuran / 8 h / Heating View Scheme
Multi-step reaction with 3 steps 1: 85 percent / BH3*SMe2 / tetrahydrofuran / 2 h / Heating 2: 90 percent / K2CO3 / CH2Cl2; H2O / 0.58 h / 20 °C 3: 88 percent / LiAlH4 / tetrahydrofuran / 1 h / Heating View Scheme
Multi-step reaction with 3 steps 1: BH3*SMe2 / tetrahydrofuran / 2.5 h / Heating 3: LAH View Scheme

: 130194-42-2
(1S)-3-amino-1-phenyl-1-propanol

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: aq. K2CO3 / CH2Cl2 / 0.5 h / 20 °C 2: 4.10 g / LiAlH4 / tetrahydrofuran / 8 h / Heating View Scheme
Multi-step reaction with 2 steps 1: 90 percent / K2CO3 / CH2Cl2; H2O / 0.58 h / 20 °C 2: 88 percent / LiAlH4 / tetrahydrofuran / 1 h / Heating View Scheme
Multi-step reaction with 2 steps 2: LAH View Scheme
Multi-step reaction with 2 steps 1: NaHCO3 2: LiAlH4 / tetrahydrofuran / Heating View Scheme

: 98-86-2
acetophenone

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: HCl / ethanol / 110 °C 2: 90 percent / hydrogen; K2CO3 / [Rh{(SC,RP)-duanphos}(norbornadiene)]SbF6 / methanol / 12 h / 20 °C / 7500.6 Torr View Scheme
Multi-step reaction with 2 steps 1: toluene-4-sulfonic acid / ethanol / 20 h / 110 °C 2: Rh[((S,S)-BenzP*)(cod)]SbF6; zinc(II) chloride; caesium carbonate; hydrogen / methanol / 20 h / 20 °C / 19001.3 Torr / Autoclave View Scheme

: 118856-08-9
butyric acid 2-ethoxycarbonyl-1-phenyl-ethyl ester

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: Candida rugosa lipase; MgCl2 / H2O; diisopropyl ether / 24 h / 30 °C 2: 95 percent / LiAlH4 / tetrahydrofuran / 1 h / 20 °C 3: 85 percent / Et3N / diethyl ether / 3 h / -10 - 0 °C / cooling 4: 82 percent / tetrahydrofuran; H2O / 4 h / 60 - 65 °C View Scheme

: 838841-85-3
(3S) ethyl β-butyryloxy-β-phenyl propionate

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 95 percent / LiAlH4 / tetrahydrofuran / 1 h / 20 °C 2: 85 percent / Et3N / diethyl ether / 3 h / -10 - 0 °C / cooling 3: 82 percent / tetrahydrofuran; H2O / 4 h / 60 - 65 °C View Scheme

: 5764-85-2
Ethyl 3-hydroxy-3-phenylpropanoate

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1: DCC; 4-(dimethylamino)pyridine / CH2Cl2 / 20 °C 2: Candida rugosa lipase; MgCl2 / H2O; diisopropyl ether / 24 h / 30 °C 3: 95 percent / LiAlH4 / tetrahydrofuran / 1 h / 20 °C 4: 85 percent / Et3N / diethyl ether / 3 h / -10 - 0 °C / cooling 5: 82 percent / tetrahydrofuran; H2O / 4 h / 60 - 65 °C View Scheme
Multi-step reaction with 3 steps 1.1: 85 percent / lithium aluminum hydride / tetrahydrofuran / 2 h 2.1: 95 percent / Et3N / CH2Cl2 / 0 h / -10 °C 3.1: O2; (-)-sparteine; 3 Angstroem sieves / Pd(OAc)2 / toluene / 36 h / 80 °C / 760 Torr 3.2: H2O / tetrahydrofuran / 65 °C View Scheme

: 96854-34-1
(S)-3-phenyl-1,3-propanediol

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 85 percent / Et3N / diethyl ether / 3 h / -10 - 0 °C / cooling 2: 82 percent / tetrahydrofuran; H2O / 4 h / 60 - 65 °C View Scheme
Multi-step reaction with 3 steps 1: 85 percent / Et3N / diethyl ether / 2 h / 0 °C 2: 90 percent / NaI / acetone / Heating 3: 86 percent / tetrahydrofuran; H2O / Ambient temperature View Scheme
Multi-step reaction with 2 steps 1: 85 percent / Et3N / diethyl ether / 2 h / 0 °C 2: 90 percent / tetrahydrofuran; H2O / 4 h / 70 °C View Scheme

: 100-52-7
benzaldehyde

SASRIN-maleidobenzoic acid resin: SASRIN-maleidobenzoic acid resin

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 6 steps 1.1: LDA / tetrahydrofuran; hexane / 1 h / -78 °C 1.2: tetrahydrofuran; hexane / 1 h / -78 °C 2.1: DCC; 4-(dimethylamino)pyridine / CH2Cl2 / 20 °C 3.1: Candida rugosa lipase; MgCl2 / H2O; diisopropyl ether / 24 h / 30 °C 4.1: 95 percent / LiAlH4 / tetrahydrofuran / 1 h / 20 °C 5.1: 85 percent / Et3N / diethyl ether / 3 h / -10 - 0 °C / cooling 6.1: 82 percent / tetrahydrofuran; H2O / 4 h / 60 - 65 °C View Scheme

Yield

Multi-step reaction with 6 steps
1.1: LDA / tetrahydrofuran; hexane / 1 h / -78 °C
1.2: tetrahydrofuran; hexane / 1 h / -78 °C
2.1: DCC; 4-(dimethylamino)pyridine / CH2Cl2 / 20 °C
3.1: Candida rugosa lipase; MgCl2 / H2O; diisopropyl ether / 24 h / 30 °C
4.1: 95 percent / LiAlH4 / tetrahydrofuran / 1 h / 20 °C
5.1: 85 percent / Et3N / diethyl ether / 3 h / -10 - 0 °C / cooling
6.1: 82 percent / tetrahydrofuran; H2O / 4 h / 60 - 65 °C
View Scheme

: (6S)-2-((S)-1-triisopropylsilyloxyethyl)-3-methyl-6-phenyl-1,3-oxazinan-4-one

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: diphenyl silane / tris(triphenylphosphine)rhodium(I) carbonyl hydride / tetrahydrofuran / 15 h / 20 °C 2: 67 percent / HCl / methanol; H2O / 1.5 h / 90 °C View Scheme

: 73627-97-1, 121617-17-2, 132203-26-0, 17190-29-3
3-hydroxy-3-phenylpropanenitrile

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: LiAlH4 / tetrahydrofuran / 5 h / Heating 2: 41 percent / Et3N / CH2Cl2 / 2 h / 23 °C 3: (-)-sparteine; O2; Molecular sieves 3A / Pd(nbd)Cl2 / toluene / 24 h / 80 °C / 760.05 Torr 4: 78 percent / LiAlH4 / tetrahydrofuran / 5.5 h / Heating View Scheme
Multi-step reaction with 3 steps 1: hydrogen, NH3 / Raney Ni / ethanol / 90 °C / p(NH3) = 30 psi and p(H2) = 170 psi 2: NaHCO3 3: LiAlH4 / tetrahydrofuran / Heating View Scheme

: 5053-63-4
3-amino-1-phenylpropan-1-ol

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 41 percent / Et3N / CH2Cl2 / 2 h / 23 °C 2: (-)-sparteine; O2; Molecular sieves 3A / Pd(nbd)Cl2 / toluene / 24 h / 80 °C / 760.05 Torr 3: 78 percent / LiAlH4 / tetrahydrofuran / 5.5 h / Heating View Scheme

: 333387-97-6
(3-oxo-3-phenylpropyl)carbamic acid tert-butyl ester

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 100 percent / NaBH4 / ethanol / 3 h / 0 - 23 °C 2: (-)-sparteine; O2; Molecular sieves 3A / Pd(nbd)Cl2 / toluene / 24 h / 80 °C / 760.05 Torr 3: 78 percent / LiAlH4 / tetrahydrofuran / 5.5 h / Heating View Scheme

: 257892-43-6
(+/-)-N-(tert-butoxycarbonyl)-3-amino-1-phenylpropan-1-ol

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: (-)-sparteine; O2; Molecular sieves 3A / Pd(nbd)Cl2 / toluene / 24 h / 80 °C / 760.05 Torr 2: 78 percent / LiAlH4 / tetrahydrofuran / 5.5 h / Heating View Scheme

: 4850-49-1
1-phenyl-1,3-propanediol

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1.1: 95 percent / Et3N / CH2Cl2 / 0 h / -10 °C 2.1: O2; (-)-sparteine; 3 Angstroem sieves / Pd(OAc)2 / toluene / 36 h / 80 °C / 760 Torr 2.2: H2O / tetrahydrofuran / 65 °C View Scheme

: 20780-53-4
(R)-Styrene oxide

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: 85.2 percent / Et3N / tetrahydrofuran / 18 h / Heating 2: BH3*SMe2 / tetrahydrofuran / 2.5 h / Heating 4: LAH View Scheme

: 100306-34-1
3-chloro-1-phenylpropanol

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 100 percent / NaI / acetone / Heating 2: 85 percent / tetrahydrofuran / Ambient temperature View Scheme
Multi-step reaction with 2 steps 1: sodium iodide / acetone / 17 h / Reflux 2: water; tetrahydrofuran / 22 h View Scheme

: 7647-01-0
hydrogenchloride

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

: 134619-77-5
(-)-N-tert-butoxycarbonyl-N-methyl-3-phenyl-3-hydroxypropylamine

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran; ethyl acetate	97%

: 24424-99-5
di-tert-butyl dicarbonate

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

: 134619-77-5
(-)-N-tert-butoxycarbonyl-N-methyl-3-phenyl-3-hydroxypropylamine

Conditions

Conditions	Yield
In dichloromethane	95%
In dichloromethane for 2h; Heating;	95%
In tetrahydrofuran at 0 - 20℃;	57%
With triethylamine In tetrahydrofuran at 0 - 20℃; for 22h;

: 402-44-8
4-Fluorobenzotrifluoride

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

: 100568-02-3
(S)-fluoxetine

Conditions

Conditions	Yield
Stage #1: (S)-N-methyl-3-amino-1-phenyl-1-propanol With sodium hydride In N,N-dimethyl acetamide; paraffin oil at 90℃; for 0.5h; Inert atmosphere; Stage #2: 4-Fluorobenzotrifluoride In N,N-dimethyl acetamide; paraffin oil at 100℃; for 5h; Inert atmosphere;	91%
With sodium hydride 1.) dimethylacetamide, 70 deg C, 30 min; 2) dimethylacetamide, 93 deg C, 2.25 h; Yield given. Multistep reaction;

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

: 98-56-6
4-chlorobenzotrifluoride

: 114247-06-2
(S)-fluoxetine hydrochloride

Conditions

Conditions	Yield
Stage #1: (S)-N-methyl-3-amino-1-phenyl-1-propanol With sodium hydride In dimethyl sulfoxide at 70℃; for 0.5h; Stage #2: 4-chlorobenzotrifluoride In dimethyl sulfoxide at 90℃; for 2h;	90%
With hydrogenchloride; sodium hydride 1) DMAC 2) EtOH; Multistep reaction;
1) DMSO, 50 deg C, 20 min, 2) DMSO, 90 deg C, 40 min; Yield given. Multistep reaction;
With hydrogenchloride; N,N-dimethyl acetamide; sodium hydride Yield given;

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

: 98-56-6
4-chlorobenzotrifluoride

: 100568-02-3
(S)-fluoxetine

Conditions

Conditions	Yield
With sodium hydride In dimethyl sulfoxide at 90 - 100℃; for 1.5h;	84%
With sodium hydride In dimethyl sulfoxide at 90 - 100℃; for 1h;	71%
With sodium hydride 1.) N,N-dimethylacetamid (DMAC), 90 deg C, 2.) 100-105 deg C; Yield given. Multistep reaction;

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

: 95-48-7
ortho-cresol

: 105314-52-1, 105314-53-2, 63940-51-2, 83015-26-3
(R)-tomoxetine

Conditions

Conditions	Yield
With triphenylphosphine; diethylazodicarboxylate In toluene at 120℃; for 2h; Solvent; Reagent/catalyst; Temperature; Mitsunobu Displacement;	79.45%
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 20℃; for 12h;	67%
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 20℃; Mitsunobu Displacement;

: 95-52-3
2-Fluorotoluene

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

: rac-tomoxetine hydrochloride

Conditions

Conditions	Yield
With sodium hydride 1) DMSO, 2) DMSO; Yield given. Multistep reaction;

: 95-49-8
2-methylchlorobenzene

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

: 105314-53-2
(S)-N-methyl-3-(2-methylphenoxy)-3-phenyl-1-propanamine

Conditions

Conditions	Yield
With 2,4-dichlorophenoxyacetic acid dimethylamine; sodium hydride Multistep reaction;

: 766-51-8
2-Chloroanisole

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

: 112066-66-7
(S)-N-methyl-3-(2-methoxyphenoxy)-3-phenyl-1-propanamine

Conditions

Conditions	Yield
With 2,4-dichlorophenoxyacetic acid dimethylamine; sodium hydride Multistep reaction;

: 114133-37-8
(S)-N-methyl-3-amino-1-phenyl-1-propanol

: 98-56-6
4-chlorobenzotrifluoride

A: 54910-89-3, 57226-07-0, 100568-02-3, 100568-03-4
(R)-fluoxetine

B: 100568-02-3
(S)-fluoxetine

Conditions

Conditions	Yield
With sodium hydride In N,N-dimethyl acetamide Title compound not separated from byproducts.;

...Expand

Related products

1141-38-4

2,6-Naphthalenedicarboxylicacid

1141-39-5

Ethanone,1-(4'-amino[1,1'-biphenyl]-4-yl)-

114144-16-0

6-Iodo-2,3-dihydro-1H-indole

114152-19-1

Benzenemethanol,2,3,6-trifluoro-

114152-21-5

Benzeneacetonitrile,2,3,6-trifluoro-

114152-23-7

Benzeneacetic acid,2,3,6-trifluoro-

1141-59-9

1,3-Benzenediol,4-[2-(2-pyridinyl)diazenyl]-

114162-64-0

beta-D-Glucopyranosiduronic acid, 5-bromo-4-chloro-1H-indol-3-yl,compd. with cyclohexanamine (1:1)

114165-30-9

Ethanone,1-(5-bromo-3-hydroxy-1H-indol-1-yl)-

114168-48-8

Benzoic acid,4-amino-2,6-dinitro-

Products

Refine

Country

Business Type

Certificate

Display

Dayang Chem (Hangzhou) Co.,Ltd.

Chemwill Asia Co., Ltd.

Hebei Nengqian Chemical Import and Export Co., LTD

Henan Wentao Chemical Product Co., Ltd.

SHANGHAI T&W PHARMACEUTICAL CO., LTD.

Zibo Hangyu Biotechnology Development Co., Ltd

GIHI CHEMICALS CO.,LIMITED

Henan Tianfu Chemical Co., Ltd.

Antimex Chemical Limied

BOC Sciences

Hangzhou Fandachem Co.,Ltd

SAGECHEM LIMITED

Chemlyte Solutions

ZHEJIANG JIUZHOU CHEM CO.,LTD

Amadis Chemical Co., Ltd.

ORCHID CHEMICAL SUPPLIES LTD

Finetech Industry Limited

Debye Scientific

Langchem

Alchemist-pharm chemical Technology Co. Ltd.

crucell inc

Synthetic route

Related products

Hot Products