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
Cas:643-20-9
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiry1.In No Less 10 years exporting experience. you can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specializ
Cas:643-20-9
Min.Order:1 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:643-20-9
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
inquiryWe 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:643-20-9
Min.Order:1 Metric Ton
FOB Price: $1.0
Type:Trading Company
inquiryOur own factory produces direct sales with absolute price advantage Application:Pharmaceutical industry Transportation:By sea Port:Shanghai/tianjin
Cas:643-20-9
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryWe are committed to providing our customers with the best products and services at the most competitive prices.Appearance:white to beige crystals Storage:Room temperature with sealed well Package:according to the clients requirement Application:Use a
Cas:643-20-9
Min.Order:0
Negotiable
Type:Trading Company
inquiry1H-Pyrrolizine,hexahydro- cas 643-20-9Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
factory?direct?sale Application:Fine chemical intermediates, used as the main raw material for the synthesis of various pesticides, medicines, surfactants, polymer monomers, and antifungal agents
Hexahydro-1H-pyrrolizine cas: 643-20-9 Storage:hermetically sealed & avoid heat, moisture and light Application:Hexahydro-1H-pyrrolizine cas: 643-20-9 Port:Tianjin
Cas:643-20-9
Min.Order:0 Metric Ton
Negotiable
Type:Trading Company
inquiry1-Benzyloxycarbonyl-5-oxoperhydroazocine
pyrrolizidine
Conditions | Yield |
---|---|
With perchloric acid; hydrogen; palladium on activated charcoal In methanol under 760.2 Torr; for 6h; Ambient temperature; | 95% |
1,2,5,6,7,8-hexahydro-3H-pyrrolizin-3-one
pyrrolizidine
Conditions | Yield |
---|---|
With dimethylsulfide borane complex In tetrahydrofuran at 20℃; for 16h; | 77% |
With lithium aluminium tetrahydride In tetrahydrofuran; diethyl ether Cooling with ice; Reflux; |
2-(3-Oxo-propyl)-pyrrolidine-1-carboxylic acid benzyl ester
pyrrolizidine
Conditions | Yield |
---|---|
With ammonium formate; palladium on activated charcoal In methanol for 0.5h; Heating; | 55% |
Conditions | Yield |
---|---|
With lithium bromide In water; acetonitrile for 2.5h; bicyclization by electrochemical oxidation; other cyclic amines; | 52% |
With lithium bromide In water; acetonitrile for 2.5h; electrochemical oxidation, C anode, 100 mA; | 52% |
tetrahydro-pyrrolizin-3,5-dione
pyrrolizidine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether |
Conditions | Yield |
---|---|
With methanol; ammonia at 140℃; |
4-hydroxyimino-heptanedioic acid diethyl ester
pyrrolizidine
Conditions | Yield |
---|---|
With 1,4-dioxane; copper oxide-chromium oxide at 265℃; under 257428 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
With methanol; platinum Hydrogenation.Hydrierung des Reaktionsprodukts an Kupferoxid-Chromoxid bei 250grad/340-400at; |
pyrrol-2-ylmethyl-malonic acid diethyl ester
pyrrolizidine
Conditions | Yield |
---|---|
With 1,4-dioxane; copper oxide-chromium oxide at 260℃; under 176522 Torr; Hydrogenation; |
1-iodo-3-chloro-propane
pyrrolidine tert-butylformamidine
pyrrolizidine
Conditions | Yield |
---|---|
Yield given. Multistep reaction; |
1-aza-1--4-cyclooctene
A
pyrrolizidine
B
(Z)-5-azacyclooctene
1-(2-pyridylthio)pyrrolizidine
Conditions | Yield |
---|---|
With malonic acid; 2-methylpropan-2-thiol In acetonitrile at 25℃; Irradiation; | A 28 % Chromat. B 45 % Chromat. C 24 % Chromat. |
8-chloro-8-azabicyclo<3.2.1>octane
pyrrolizidine
Conditions | Yield |
---|---|
With sodium tetrahydroborate; silver tetrafluoroborate 1.) Benzene, room temp, 4h; Yield given. Multistep reaction; |
pyrrolizidine
Conditions | Yield |
---|---|
Yield given. Multistep reaction; |
pyrrolizidine
Conditions | Yield |
---|---|
With sodium hydroxide |
pyrrolizidine
Conditions | Yield |
---|---|
With sodium hydroxide |
pyrrolizidine
Conditions | Yield |
---|---|
With sodium hydroxide |
1,4-dioxane
3-(5-oxo-4,5-dihydro-pyrrol-2-yl)-propionic acid amide
pyrrolizidine
Conditions | Yield |
---|---|
at 250℃; under 95616 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
at 250℃; under 250073 - 301558 Torr; Irradiation; |
1,4-dioxane
4-hydroxyimino-heptanedioic acid diethyl ester
pyrrolizidine
Conditions | Yield |
---|---|
at 265℃; under 257428 Torr; Hydrogenation; |
pyrrolizidine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether | 0.09 g |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 65 percent / NaHCO3 / H2O / 1.5 h / Ambient temperature 2: 86 percent / PCC / CH2Cl2 / 3 h / Ambient temperature 3: 55 percent / ammonium formate / Pd/C / methanol / 0.5 h / Heating View Scheme |
pyrrolizidine
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: 90 percent / 3N aq. HCl / 12 h / 60 °C 2: 90 percent / NaBH4 / ethanol / 48 h 3: 65 percent / NaHCO3 / H2O / 1.5 h / Ambient temperature 4: 86 percent / PCC / CH2Cl2 / 3 h / Ambient temperature 5: 55 percent / ammonium formate / Pd/C / methanol / 0.5 h / Heating View Scheme |
3-(3,4-dihydro-2H-pyrrol-5-yl)propan-1-ol
pyrrolizidine
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 90 percent / NaBH4 / ethanol / 48 h 2: 65 percent / NaHCO3 / H2O / 1.5 h / Ambient temperature 3: 86 percent / PCC / CH2Cl2 / 3 h / Ambient temperature 4: 55 percent / ammonium formate / Pd/C / methanol / 0.5 h / Heating View Scheme |
2-(3-Hydroxy-propyl)-pyrrolidine-1-carboxylic acid benzyl ester
pyrrolizidine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 86 percent / PCC / CH2Cl2 / 3 h / Ambient temperature 2: 55 percent / ammonium formate / Pd/C / methanol / 0.5 h / Heating View Scheme |
pyrrolizidine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 68 percent / PPh3, HN3, E-N=N-E View Scheme |
benzyl diallylcarbamate
pyrrolizidine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: 95 percent / perchloric acid, hydrogen / 10percent Pd/C / methanol / 6 h / 760.2 Torr / Ambient temperature View Scheme | |
Multi-step reaction with 2 steps 2: 95 percent / perchloric acid, hydrogen / 10percent Pd/C / methanol / 6 h / 760.2 Torr / Ambient temperature View Scheme | |
Multi-step reaction with 2 steps 2: 95 percent / perchloric acid, hydrogen / 10percent Pd/C / methanol / 6 h / 760.2 Torr / Ambient temperature View Scheme |
2-(N,N-dimethylaminomethyl)pyrrole
pyrrolizidine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: ethanol / anschliessendes Erwaermen mit der Natrium-Verbindung des Malonsaeure-diaethylesters in Aethanol 2: copper oxide-chromium oxide; dioxane / 260 °C / 176522 Torr / Hydrogenation View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: acetic acid anhydride / Erhitzen auf Siedetemperatur 2: lithium alanate; diethyl ether View Scheme |
3H-pyrrolizine
A
pyrrolizidine
B
2-n-propylpyrrole
C
1,2-dihydro-3H-pyrrolo<1,2-a>pyrrole
Conditions | Yield |
---|---|
With 5% Pd(II)/C(eggshell); hydrogen In ethanol at 20℃; under 2844.39 Torr; for 8h; | A n/a B 7 mg C 16 mg |
Conditions | Yield |
---|---|
In propan-1-ol Heating; | 56% |
pyrrolizidine
2-Bromoethyl cyclopentylphenylacetate
1-(2-Hydroxyethyl)pyrrolizidinium bromide α-phenylcyclopentaneacetate
Conditions | Yield |
---|---|
In diethyl ether | 40% |
pyrrolizidine
methyl iodide
cis-4-methyl-hexahydro-pyrrolizinium; iodide
Conditions | Yield |
---|---|
With diethyl ether |
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