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Cas:3852-09-3
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inquiryUnique advantages of Methyl 3-methoxypropionate Cas 3852-09-3 Guaranteed purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:Transparent colorless liquid Storage:Cool dry place Package
Cas:3852-09-3
Min.Order:200 Kilogram
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inquiryThe 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
Name: Methyl 3-methoxypropionate CAS:3852-09-3 MF: C5H10O3 Appearance:Corlorless Liquid Storage:Preserve in well-closed, light-resistant and airtight containers. Package:25kg Application:Syntheses Material Intermediates Transportation:By sea Port
Cas:3852-09-3
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inquiryWith our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufacturin
Cas:3852-09-3
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inquiryTIANFUCHEM--3852-09-3--High purity Methyl 3-methoxypropionate factory price Our company was built in 2009 with an ISO certificate.In the past 10 years, we have grown up as a famous fine chemicals supplier in China And we had established st
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Cas:3852-09-3
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Cas:3852-09-3
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Cas:3852-09-3
Min.Order:1 Kilogram
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inquiry★.Best quality according to requirement ★.Competitive price in China market ★.Mature Technical support ★.Professional logistic support ★.Shortest delivery time . Appearance:Colorless transparent liquid. Storage:store in a cool, dry place. P
Cas:3852-09-3
Min.Order:1 Kilogram
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inquiryMethyl 3-methoxypropionate CAS:3852-09-3 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
Cas:3852-09-3
Min.Order:1 Gram
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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:3852-09-3
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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
Appearance:off-white to white solid Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for Synthesis API and Research Transportation:By Sea/Air/Courier Port:Qingdao
Cas:3852-09-3
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inquiryour strengths: 1: Fast and guaranteed shipment (TNT;EMS;FEDEX;DHL;UPS;EUB, special line) 2: Various payment items accepted (Btc; MoneyGram; WU) 3: Valued package (Paraffin coating; Double aluminum foil bag; Vacuum packaging) 4: Efficient delivery
Cas:3852-09-3
Min.Order:1 Gram
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Type:Other
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:3852-09-3
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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:3852-09-3
Min.Order:10 Gram
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Cas:3852-09-3
Min.Order:100 Gram
FOB Price: $100.0 / 2000.0
Type:Lab/Research institutions
inquiryProduct name: Methyl 3-Methoxypropionate CAS No.:3852-09-3 Molecule Formula:C5H10O3 Molecule Weight:118.13 Purity: 99% Package: 25kg/drum Description:White powder Manufacture Standards:Enterprise Standard TESTING ITEMS
Cas:3852-09-3
Min.Order:1 Kilogram
Negotiable
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
Cas:3852-09-3
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inquiryMethyl 3-methoxypropionate Basic information Product Name: Methyl 3-methoxypropionate Synonyms: Methyl β-Methoxypropionate;Methyl 3-methoxypropionate,98%;Methyl 3-methoxyprop;3-Methoxy propionate;Methyl 3-methoxypropiote;METHYL 3-METHOXYP
Cas:3852-09-3
Min.Order:1 Gram
Negotiable
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:3852-09-3
Min.Order:1 Kilogram
FOB Price: $18.0 / 20.0
Type:Trading Company
inquiryShandong Mopai Biotechnology 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 chemicals. W
Cas:3852-09-3
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiry1.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
Cas:3852-09-3
Min.Order:1 Metric Ton
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Type:Trading Company
inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
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:3852-09-3
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
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Min.Order:0
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Type:Trading Company
inquiryConditions | Yield |
---|---|
With sodium methylate at 60℃; for 8h; | 99% |
With sodium methylate; 4-methoxy-phenol at 40 - 60℃; for 6h; Temperature; Reagent/catalyst; | 99% |
With triethylamine at 20℃; for 8h; Temperature; Reagent/catalyst; Large scale; | 98% |
sodium methylate
acrylic acid methyl ester
methyl 3-methoxypropionate
Conditions | Yield |
---|---|
With 4-methoxy-phenol In methanol at 40 - 60℃; for 6h; Reagent/catalyst; | 99% |
In methanol for 24h; Heating; | 54% |
lithium methanolate
acrylic acid methyl ester
methyl 3-methoxypropionate
Conditions | Yield |
---|---|
With hydroquinone In methanol at 40℃; for 20h; | 88% |
methanol
A
Methyl 3-bromopropionate
B
methyl 3-methoxypropionate
C
ethylene dibromide
D
2-Bromoethyl methyl ether
Conditions | Yield |
---|---|
With bromine at -80℃; temperature up to 30 deg C; | A 67% B n/a C n/a D n/a |
acrylic acid methyl ester
B
methyl 3-methoxypropionate
Conditions | Yield |
---|---|
With sodium methylate In methanol | A 65% B n/a |
acrylic acid methyl ester
cyclohexanol
A
methyl 3-methoxypropionate
B
cyclohexyl acrylate
C
3-Methoxy-propionic acid cyclohexyl ester
Conditions | Yield |
---|---|
With n-butyllithium; bis(acetylacetonate)nickel(II) In benzene at 90℃; for 5h; Product distribution; | A 22% B 23% C 52% |
2-pentanol
acrylic acid methyl ester
A
methyl 3-methoxypropionate
B
3-pentyl acrylate
C
3-Methoxy-propionic acid 1-ethyl-propyl ester
Conditions | Yield |
---|---|
With n-butyllithium; bis(acetylacetonate)nickel(II) In benzene at 90℃; for 5h; Product distribution; other temp., other time; | A 19% B 25% C 48% |
acrylic acid methyl ester
isopropyl alcohol
A
methyl 3-methoxypropionate
B
isopropyl acrylate
C
isopropyl 3-methoxypropionate
D
3-isopropoxy-propionic acid isopropyl ester
Conditions | Yield |
---|---|
With n-butyllithium; bis(acetylacetonate)nickel(II) In benzene at 90℃; for 5h; Product distribution; other temp, other time; | A 17% B 15% C 42% D 26% |
acrylic acid methyl ester
iso-butanol
A
methyl 3-methoxypropionate
B
sec-butyl acrylate
C
3-methoxy-propionic acid sec-butyl ester
D
3-sec-butoxy-propionic acid sec-butyl ester
Conditions | Yield |
---|---|
With n-butyllithium; bis(acetylacetonate)nickel(II) In benzene at 90℃; for 5h; Product distribution; | A 27% B 28% C 33% D 6% |
acrylic acid methyl ester
tert-butyl alcohol
A
tert-Butyl acrylate
B
methyl 3-methoxypropionate
C
3-tert.-Butoxypropionsaeuremethylester
D
3-Methoxy-propionic acid tert-butyl ester
E
tert-butyl β-tert-butoxypropionate
Conditions | Yield |
---|---|
With n-butyllithium; bis(acetylacetonate)nickel(II) In benzene at 90℃; for 5h; Product distribution; other time, other temp.; | A 33% B 26% C 9% D 32% E 3% |
(1S,2R,5S)-(+)-menthol
acrylic acid methyl ester
A
methyl 3-methoxypropionate
B
(1S,2R,5S)‐2‐isopropyl‐5‐methylcyclohexyl acrylate
Conditions | Yield |
---|---|
With n-butyllithium; bis(acetylacetonate)nickel(II) In benzene at 90℃; for 5h; Product distribution; | A 22% B 23% |
methanol
levulinic acid methyl ester
A
methyl 3,3-dimethoxypropionate
B
acetic acid methyl ester
C
methyl 3-methoxypropionate
D
malonic acid dimethyl ester
E
Dimethyl succinate
Conditions | Yield |
---|---|
With dihydrogen peroxide; toluene-4-sulfonic acid In water at 80℃; for 6h; Reagent/catalyst; Solvent; Baeyer-Villiger Ketone Oxidation; Overall yield = 22 %; | A 13% B n/a C n/a D 8% E n/a |
Conditions | Yield |
---|---|
at -80 - 10℃; in Gegenwart von sauren Katalysatoren; | |
With boron trifluoride at -80℃; |
Conditions | Yield |
---|---|
With sulfuric acid at 65℃; |
methanol
acrylic acid methyl ester
A
3-Methoxypropionic acid
B
methyl 3-methoxypropionate
Conditions | Yield |
---|---|
With sodium |
Conditions | Yield |
---|---|
beim nachfolgendes Kochen; |
methanol
3-(N-Nitroso-methoxycarbonylamino)-propionsaeure-methylester
methyl 3-methoxypropionate
Conditions | Yield |
---|---|
With potassium carbonate |
Conditions | Yield |
---|---|
In diethyl ether |
Conditions | Yield |
---|---|
In methanol |
methyl vinyl ketone
acrylic acid methyl ester
A
1-methoxybutan-3-one
B
methyl 3-methoxypropionate
Conditions | Yield |
---|---|
With sodium hydroxide; cetyltrimethylammonim bromide In dichloromethane | A 28 % Chromat. B 10 % Chromat. |
thiophenol
acrylic acid methyl ester
A
methyl 3-methoxypropionate
B
methyl 3-phenylthiopropanoate
Conditions | Yield |
---|---|
With sodium 1.) methanol; 2.) reflux, 1 h; Yield given. Multistep reaction. Yields of byproduct given; |
methanol
acrylic acid methyl ester
A
methyl 3-methoxypropionate
B
methyl 3-phenylthiopropanoate
Conditions | Yield |
---|---|
With sodium; thiophenol 1.) methanol; 2.) reflux, 1 h; Yield given. Multistep reaction. Yields of byproduct given; |
methanol
acrylic acid
A
methyl 3-methoxypropionate
B
acrylic acid methyl ester
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid at 111.1℃; for 0.25h; Product distribution; Kinetics; other times, temp.; |
methanol
acrylic acid methyl ester
A
methyl 3,3-dimethoxypropionate
B
methyl (2E)-3-methoxy-2-propenoate
C
methyl 3-methoxypropionate
Conditions | Yield |
---|---|
With supercritical CO2; oxygen; copper dichloride; palladium dichloride at 40℃; for 12h; Product distribution; various catalysts and temperatures; | |
With supercritical CO2; oxygen; copper dichloride; palladium dichloride at 40℃; for 12h; | A 91.7 % Chromat. B 1.2 % Chromat. C 2.0 % Chromat. |
With supercritical CO2; oxygen; dichloro bis(acetonitrile) palladium(II); copper dichloride at 50℃; for 12h; | A 81.1 % Chromat. B 8.8 % Chromat. C 3.5 % Chromat. |
With supercritical CO2; oxygen; copper dichloride; palladium dichloride at 50℃; for 12h; | A 42.9 % Chromat. B 3.1 % Chromat. C 6.6 % Chromat. |
Ketene
Dimethoxymethane
sulfuric acid
methyl 3-methoxypropionate
Conditions | Yield |
---|---|
at 4℃; |
Ketene
Dimethoxymethane
boron trifluoride
methyl 3-methoxypropionate
Conditions | Yield |
---|---|
at -80℃; |
Conditions | Yield |
---|---|
at 4℃; |
methyl 3-methoxypropionate
dimethyl amine
β-methoxy-N,N-dimethylpropionic acid amide
Conditions | Yield |
---|---|
With zinc(II) trifluoroacetate at 0 - 40℃; for 8h; Reagent/catalyst; Autoclave; | 99% |
With sodium methylate; glycerol at 60℃; for 6h; Autoclave; | 86% |
With potassium tert-butylate at 20℃; under 600.06 Torr; for 4h; Product distribution / selectivity; Autoclave; | |
With sodium methylate; ethylene glycol at 60℃; for 8h; Product distribution / selectivity; Autoclave; |
methyl 3-methoxypropionate
(RS)-1-methyl-3-phenylpropylamine
(R)-3-methoxy-N-(4-phenylbutan-2-yl)propanamide
Conditions | Yield |
---|---|
With Candida antarctica lipase B; Octanethiol; [Ir(2-phenylpyridine)2(4,4′-di-tert-butyl-2,2′-bipyridine)](PF6) In acetonitrile at 38℃; for 24h; Concentration; Schlenk technique; Molecular sieve; Inert atmosphere; Irradiation; Enzymatic reaction; enantioselective reaction; | 98% |
Conditions | Yield |
---|---|
With iron(II) triflate In N,N-dimethyl-formamide at 80℃; for 2h; | 98% |
methyl 3-methoxypropionate
2-amino-1-phenylpropane
(R)-3-methoxy-N-(1-phenylpropan-2-yl)propanamide
Conditions | Yield |
---|---|
With Candida antarctica lipase B; Octanethiol; [Ir(2-phenylpyridine)2(4,4′-di-tert-butyl-2,2′-bipyridine)](PF6) In acetonitrile at 38℃; for 72h; Schlenk technique; Molecular sieve; Inert atmosphere; Irradiation; Enzymatic reaction; enantioselective reaction; | 97% |
methyl 3-methoxypropionate
Conditions | Yield |
---|---|
With Candida antarctica lipase B; Octanethiol; [Ir(2-phenylpyridine)2(4,4′-di-tert-butyl-2,2′-bipyridine)](PF6) In acetonitrile at 38℃; for 72h; Schlenk technique; Molecular sieve; Inert atmosphere; Irradiation; Enzymatic reaction; enantioselective reaction; | 96% |
methyl 3-methoxypropionate
Conditions | Yield |
---|---|
With Candida antarctica lipase B; Octanethiol; [Ir(2-phenylpyridine)2(4,4′-di-tert-butyl-2,2′-bipyridine)](PF6) In acetonitrile at 38℃; for 72h; Schlenk technique; Molecular sieve; Inert atmosphere; Irradiation; Enzymatic reaction; enantioselective reaction; | 95% |
Conditions | Yield |
---|---|
With Candida antarctica lipase B; Octanethiol; [Ir(2-phenylpyridine)2(4,4′-di-tert-butyl-2,2′-bipyridine)](PF6) In acetonitrile at 38℃; for 72h; Schlenk technique; Molecular sieve; Inert atmosphere; Irradiation; Enzymatic reaction; enantioselective reaction; | 95% |
Conditions | Yield |
---|---|
With Candida antarctica lipase B; Octanethiol; [Ir(2-phenylpyridine)2(4,4′-di-tert-butyl-2,2′-bipyridine)](PF6) In acetonitrile at 38℃; for 72h; Schlenk technique; Molecular sieve; Inert atmosphere; Irradiation; Enzymatic reaction; enantioselective reaction; | 94% |
Conditions | Yield |
---|---|
With Candida antarctica lipase B; Octanethiol; [Ir(2-phenylpyridine)2(4,4′-di-tert-butyl-2,2′-bipyridine)](PF6) In acetonitrile at 38℃; for 72h; Schlenk technique; Molecular sieve; Inert atmosphere; Irradiation; Enzymatic reaction; enantioselective reaction; | 94% |
methyl 3-methoxypropionate
Conditions | Yield |
---|---|
With lithium deuteride In diethyl ether for 1h; Heating; | 91% |
With lithium aluminium deuteride | 54% |
With lithium aluminium deuteride | 1.82 g |
methyl 3-methoxypropionate
Conditions | Yield |
---|---|
With Candida antarctica lipase B; Octanethiol; [Ir(2-phenylpyridine)2(4,4′-di-tert-butyl-2,2′-bipyridine)](PF6) In acetonitrile at 38℃; for 72h; Schlenk technique; Molecular sieve; Inert atmosphere; Irradiation; Enzymatic reaction; enantioselective reaction; | 87% |
methyl 3-methoxypropionate
1-methyl-3-p-tolyl-propylamine
Conditions | Yield |
---|---|
With Candida antarctica lipase B; Octanethiol; [Ir(2-phenylpyridine)2(4,4′-di-tert-butyl-2,2′-bipyridine)](PF6) In acetonitrile at 38℃; for 72h; Schlenk technique; Molecular sieve; Inert atmosphere; Irradiation; Enzymatic reaction; enantioselective reaction; | 85% |
methyl 3-methoxypropionate
1-cyclohexylethylamine
Conditions | Yield |
---|---|
With Candida antarctica lipase B; Octanethiol; [Ir(2-phenylpyridine)2(4,4′-di-tert-butyl-2,2′-bipyridine)](PF6) In acetonitrile at 38℃; for 72h; Schlenk technique; Molecular sieve; Inert atmosphere; Irradiation; Enzymatic reaction; enantioselective reaction; | 84% |
Conditions | Yield |
---|---|
With Candida antarctica lipase B; Octanethiol; [Ir(2-phenylpyridine)2(4,4′-di-tert-butyl-2,2′-bipyridine)](PF6) In acetonitrile at 38℃; for 60h; Schlenk technique; Molecular sieve; Inert atmosphere; Irradiation; Enzymatic reaction; enantioselective reaction; | 81% |
Conditions | Yield |
---|---|
With iron(II) triflate In N,N-dimethyl-formamide at 0 - 90℃; for 1h; Autoclave; | 79% |
Conditions | Yield |
---|---|
With iron(II) triflate at 0 - 40℃; under 760.051 Torr; for 1h; Autoclave; | 79% |
rac-2-aminooctane
methyl 3-methoxypropionate
(R)-3-methoxy-N-(octan-2-yl) propanamide
Conditions | Yield |
---|---|
With Candida antarctica lipase B; Octanethiol; [Ir(2-phenylpyridine)2(4,4′-di-tert-butyl-2,2′-bipyridine)](PF6) In acetonitrile at 38℃; for 72h; Schlenk technique; Molecular sieve; Inert atmosphere; Irradiation; Enzymatic reaction; enantioselective reaction; | 79% |
With novozyme 435 In cyclohexane at 70℃; under 7500.75 Torr; for 24h; Resolution of racemate; Inert atmosphere; Autoclave; Enzymatic reaction; |
Conditions | Yield |
---|---|
With Candida antarctica lipase B; Octanethiol; [Ir(2-phenylpyridine)2(4,4′-di-tert-butyl-2,2′-bipyridine)](PF6) In acetonitrile at 38℃; for 72h; Schlenk technique; Molecular sieve; Inert atmosphere; Irradiation; Enzymatic reaction; enantioselective reaction; | 78% |
methyl 3-methoxypropionate
diethylamine
3-methoxy-N,N-diethylpropionic acid amide
Conditions | Yield |
---|---|
With iron(II) triflate at 0 - 100℃; for 1h; Autoclave; | 76% |
Conditions | Yield |
---|---|
With iron(II) triflate at 0 - 50℃; under 760.051 Torr; for 1h; Autoclave; | 75% |
1,5-dimethylhexylamine
methyl 3-methoxypropionate
(R)-3-methoxy-N-(6-methylheptan-2-yl) propanamide
Conditions | Yield |
---|---|
With Candida antarctica lipase B; Octanethiol; [Ir(2-phenylpyridine)2(4,4′-di-tert-butyl-2,2′-bipyridine)](PF6) In acetonitrile at 38℃; for 48h; Schlenk technique; Molecular sieve; Inert atmosphere; Irradiation; Enzymatic reaction; enantioselective reaction; | 74% |
Conditions | Yield |
---|---|
With Candida antarctica lipase B; Octanethiol; [Ir(2-phenylpyridine)2(4,4′-di-tert-butyl-2,2′-bipyridine)](PF6) In acetonitrile at 38℃; for 72h; Schlenk technique; Molecular sieve; Inert atmosphere; Irradiation; Enzymatic reaction; enantioselective reaction; | 72% |
methyl 3-methoxypropionate
4-iodo-N,N-dimethyl-1H-imidazole-1-sulfonamide
4,4'-(1-hydroxy-3-methoxypropane-1,1-diyl)bis(N,N-dimethyl-1H-imidazole-1-sulfonamide)
Conditions | Yield |
---|---|
Stage #1: 4-iodo-N,N-dimethyl-1H-imidazole-1-sulfonamide With ethylmagnesium bromide In diethyl ether; dichloromethane at 20℃; for 2h; Double Grignard reaction; Inert atmosphere; Stage #2: methyl 3-methoxypropionate In diethyl ether; dichloromethane at 20℃; for 48h; Double Grignard reaction; Inert atmosphere; Stage #3: With water; ammonium chloride In diethyl ether; dichloromethane | 71% |
N-ethylhexylamine
methyl 3-methoxypropionate
Conditions | Yield |
---|---|
With iron(II) triflate at 0 - 25℃; under 760.051 Torr; for 1h; Autoclave; | 66% |
methyl 3-methoxypropionate
(+)-(R)-1-Methyl-3-(4-methoxyphenyl)-1-propylamine
Conditions | Yield |
---|---|
With Candida antarctica lipase B; Octanethiol; [Ir(2-phenylpyridine)2(4,4′-di-tert-butyl-2,2′-bipyridine)](PF6) In acetonitrile at 38℃; for 72h; Schlenk technique; Molecular sieve; Inert atmosphere; Irradiation; Enzymatic reaction; enantioselective reaction; | 64% |
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