The 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
Cas:79874-76-3
Min.Order:1
Negotiable
Type:Other
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:79874-76-3
Min.Order:1 Kilogram
FOB Price: $139.0 / 210.0
Type:Trading Company
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:79874-76-3
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryDelmopinol CAS:79874-76-3 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 intermediates,
Cas:79874-76-3
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
Cas:79874-76-3
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryHenan 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
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Cas:79874-76-3
Min.Order:10 Gram
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Type:Lab/Research institutions
inquiryOur Advantages A. International Top level TechnologyOur company owned biomedicine experts are famous at home and abroad with rich experience in research and development in the field of efficient chiral functional molecules research and development an
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Cas:79874-76-3
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
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1.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
GOLDEN PHARMA CO.,LIMITED.is a professional pharmaceutical company,our team have more than 20years expereince in pharmaceutical production and sales. we are a professional technical enterprise specializing in the R & D, production,QA regulation
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Cas:79874-76-3
Min.Order:0
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inquiryDELMOPINOL HYDROCHLORIDEAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:pharmaceutical intermediate Transportation:by air, by sea, by express
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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Min.Order:1 Kilogram
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Type:Trading Company
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3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
Stage #1: methanesulfonic acid 1-[2-(2,2-dimethyl-oxazolidin-3-yl)-ethoxymethyl]-5-propyl-octyl ester With water at 95℃; for 17h; Stage #2: With sulfuric acid; water In toluene pH=1; Stage #3: With sodium hydroxide; water at 60℃; for 0.166667h; pH=14; Product distribution / selectivity; | 89% |
3-(4-propyl-heptyl)morpholine
2-chloro-ethanol
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
Stage #1: 3-(4-propyl-heptyl)morpholine; 2-chloro-ethanol With potassium iodide In ethanol for 5h; Reflux; Stage #2: With potassium hydroxide In ethanol for 11h; Reflux; | 70.7% |
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
With water at 95℃; for 17h; Product distribution / selectivity; | 70% |
3-(4-propyl-heptyl)morpholine
1-chloroethanol
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
With potassium hydroxide; potassium iodide In ethanol; water |
oxazolidin[2,3-c]morpholine
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
Stage #1: C10H21BrMg; oxazolidin[2,3-c]morpholine In tetrahydrofuran; toluene at 20℃; for 0.5h; Stage #2: With ammonium chloride In tetrahydrofuran; water; toluene at 40℃; |
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: ethyl bromide; magnesium / tetrahydrofuran / 3 h / 45 °C / Reflux 1.2: 1.5 h / 20 - 25 °C 2.1: 5%-palladium/activated carbon; hydrogen / methanol / 40 °C / 3750.38 Torr View Scheme | |
Multi-step reaction with 2 steps 1.1: lithium hydride / tetrahydrofuran / 20 °C / Reflux 1.2: 20 °C / Reflux 2.1: hydrogen; 5%-palladium/activated carbon / methanol / 30 °C / 2250.23 Torr View Scheme |
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
With 5%-palladium/activated carbon; hydrogen In methanol at 40℃; under 3750.38 Torr; | 323 g |
oxazolidin[2,3-c]morpholine
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
Stage #1: 1-chloro-4-propylheptane With ethyl bromide; magnesium In tetrahydrofuran at 60 - 65℃; for 3.5h; Stage #2: oxazolidin[2,3-c]morpholine In tetrahydrofuran; toluene at 0 - 5℃; | 79.2 g |
4-cyclopropylheptan-4-ol
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: hydrogenchloride / water / 10 h / 30 - 40 °C / Large scale 2.1: hydrogen; platinum on carbon / methanol / 30 °C / 2250.23 Torr 3.1: ethyl bromide; magnesium / tetrahydrofuran / 3.5 h / 60 - 65 °C 3.2: 0 - 5 °C View Scheme | |
Multi-step reaction with 3 steps 1.1: hydrogenchloride / water / 10 h / 20 - 40 °C / Large scale 2.1: ethyl bromide; magnesium / tetrahydrofuran / 3 h / 45 °C / Reflux 2.2: 1.5 h / 20 - 25 °C 3.1: 5%-palladium/activated carbon; hydrogen / methanol / 40 °C / 3750.38 Torr View Scheme | |
Multi-step reaction with 3 steps 1.1: hydrogenchloride / water / 10 h / 20 - 40 °C / Large scale 2.1: lithium hydride / tetrahydrofuran / 20 °C / Reflux 2.2: 20 °C / Reflux 3.1: hydrogen; 5%-palladium/activated carbon / methanol / 30 °C / 2250.23 Torr View Scheme |
4-(2-hydroxyethyl)morpholin-3-one
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: lithium hydride / tetrahydrofuran / 20 °C / Reflux 1.2: 20 °C / Reflux 2.1: hydrogen; 5%-palladium/activated carbon / methanol / 30 °C / 2250.23 Torr View Scheme |
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
With 5%-palladium/activated carbon; hydrogen In methanol at 30℃; under 2250.23 Torr; | 116.5 g |
4-heptanone
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: tetrahydrofuran / 12 h / 25 - 30 °C 2.1: sodium tungstate (VI) dihydrate; dihydrogen peroxide / methanol; ethanol / 18 h / 50 - 60 °C 3.1: toluene-4-sulfonic acid; hydrogen; palladium on activated charcoal / isopropyl alcohol / 15 h / 70 - 80 °C / 22502.3 Torr / Autoclave 4.1: Triphenylphosphine oxide; trifluoromethylsulfonic anhydride; sodium tetrahydroborate / dichloromethane / 12.5 h / 0 - 25 °C / Inert atmosphere 5.1: potassium iodide / ethanol / 5 h / Reflux 5.2: 11 h / Reflux View Scheme |
4-hydroxy-4-propyl-1-heptene
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: sodium tungstate (VI) dihydrate; dihydrogen peroxide / methanol; ethanol / 18 h / 50 - 60 °C 2.1: toluene-4-sulfonic acid; hydrogen; palladium on activated charcoal / isopropyl alcohol / 15 h / 70 - 80 °C / 22502.3 Torr / Autoclave 3.1: Triphenylphosphine oxide; trifluoromethylsulfonic anhydride; sodium tetrahydroborate / dichloromethane / 12.5 h / 0 - 25 °C / Inert atmosphere 4.1: potassium iodide / ethanol / 5 h / Reflux 4.2: 11 h / Reflux View Scheme |
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: toluene-4-sulfonic acid; hydrogen; palladium on activated charcoal / isopropyl alcohol / 15 h / 70 - 80 °C / 22502.3 Torr / Autoclave 2.1: Triphenylphosphine oxide; trifluoromethylsulfonic anhydride; sodium tetrahydroborate / dichloromethane / 12.5 h / 0 - 25 °C / Inert atmosphere 3.1: potassium iodide / ethanol / 5 h / Reflux 3.2: 11 h / Reflux View Scheme |
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: Triphenylphosphine oxide; trifluoromethylsulfonic anhydride; sodium tetrahydroborate / dichloromethane / 12.5 h / 0 - 25 °C / Inert atmosphere 2.1: potassium iodide / ethanol / 5 h / Reflux 2.2: 11 h / Reflux View Scheme |
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
With hydrogenchloride In Isopropyl acetate at 0℃; | 84% |
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
rac-4-(2-hydroxyethyl)-3-(4-propylheptyl) morpholine hydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride In dibutyl ether; water; ethyl acetate at 0 - 60℃; for 3h; Product distribution / selectivity; | 67% |
With hydrogenchloride In water at 0 - 60℃; for 4h; Product distribution / selectivity; | 50% |
With hydrogenchloride In water; 4-methyl-2-pentanone at 0 - 60℃; for 2h; | |
With hydrogenchloride In Isopropyl acetate at 0℃; | 93.5 g |
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
With sodium hydride In toluene; mineral oil at 0 - 25℃; for 2.16h; Reagent/catalyst; Temperature; Solvent; | 58.9% |
citric acid
3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine
Conditions | Yield |
---|---|
In ethyl acetate; isopropyl alcohol at 20 - 25℃; Temperature; Solvent; | 351.9 g |
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