Dayangchem's 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. DayangChem can provide different quantities
Cas:758-96-3
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inquiryProduct Description
Cas:758-96-3
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inquiryUnique advantages for N,N-Dimethylpropionamide Cas758-96-3 Guaranteed the purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:Colorless clear liquid Package:25kg/drum ;200kg/drum Applicatio
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inquiry1. Factory price and high quality must be guaranteed, base on 8 years of production and R&D experience 2. Free samples will be provided,ensure specifications and quality are right for customer 3. Customers will receive the most professional techn
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inquiryN,N-Dimethylpropionamide Product name: N,N-Dimethylpropionamide CAS No.: 758-96-3 Molecular formula C5H11NO Molecular weight: 101.15 Structural fo
Cas:758-96-3
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inquiryOur 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
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inquiryTIANFUCHEM--758-96-3--N,N-Dimethylpropionamide 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 stable business
Cas:758-96-3
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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:758-96-3
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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
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inquiryOur Advantage: high quality with competitive price High quality standard: BP/USP/EP Enterprise standard All purity customized Fast and safe delivery We have reliable forwarder who can help us deliver our goods more fast and safe. We
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Min.Order:10 Kilogram
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inquiry1. Product advantages High purity, all above 98.5%, no impurities after dissolution We will test each batch to ensure quality OEM and private brand services designed for free Various cap colors available We can also provide MT1 peptide powd
Cas:758-96-3
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inquiryChemical Name: N,N-Dimethylpropionamide CAS: 758-96-3 Molecular Fomula: C5H11NO Molecular weight: 101.15 Appearance: colorless liquid Assay: 99%min Appearance:Colorless transparent liquid Storage: Room Temperature Package: 25kg/drum Appli
Cas:758-96-3
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inquiryAppearance:Colorless or light yellow liquid Storage:ln stock Package:25kg/Barrel Application:Used as organic synthesis and pharmaceutical intermediates Transportation:Express/Sea/Air Port:Any port of China
Cas:758-96-3
Min.Order:25 Kilogram
FOB Price: $1.0 / 4.9
Type:Lab/Research institutions
inquiry1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; Appearance:White Crystalline Powder Storage:Store in sealed conta
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inquiry1.No Less 8 years exporting experience. Clients 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 Specialized
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Min.Order:1 Kilogram
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inquiryN,N-Dimethylpropionamide CAS: 758-96-3 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 i
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Min.Order:1 Gram
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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
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Min.Order:1 Kilogram
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inquiryAdvantage : LIDE PHARMACEUTICALS LTD. is a mid-small manufacturing-type enterprise, engaged in pharmaceutical intermediates of R&D, custom-made and production, and also involving trading chemicals for export. We have established the R&
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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
Hebei Mojin Biotechnology Co., Ltd,Our business covers more than 30 countries, most of the big customers come from Europe, America and other countries in the world, we can guarantee the quality and price. In recent decades, with the efforts of all em
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Min.Order:1 Gram
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Type:Trading Company
inquiryOur advantages: Sales term: Has a strong chemical professional quality and strong sense of responsibilit.In the sales field of fine chemicals and the market development of new products, we have a strong foresight and pertine
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryProduct Detail Minimum Order Qty. 10 Gram
Cas:758-96-3
Min.Order:10 Gram
Negotiable
Type:Trading Company
inquiry1,we produce and sell good chemicals around the world. 2,our success rate is about 95%. this means, if customer order is accepted, the probability that the customer will obtain the ordered substances, is 95%. 3,our staff consists of highly qualifie
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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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
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
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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
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inquiryWe are one of a few suppliers that can offer custom synthesis service of this product We are specialized in custom synthesis, chemical/pharmaceutical/ pesticides outsourcing and contract research. We are committed to prov
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Type:Lab/Research institutions
inquiryd'hydrazide de l'acide propionique
A
1,2,4-Triazole
B
N,N-dimethyl-propanamide
Conditions | Yield |
---|---|
In methanol for 7h; Heating; | A 87% B 91% |
triethylgermyllithium
N,N-dimethyl acetamide
A
N,N-dimethyl-propanamide
B
Triethylgerman
Conditions | Yield |
---|---|
With methyl iodide In tetrahydrofuran double excess of MeI; not isolated; GLC; | A 86% B 89% |
1-hydroxy-2-butyl-dimethylamine
N,N-dimethyl-propanamide
Conditions | Yield |
---|---|
With potassium hydroxide; air In diethyl ether at 20℃; for 90h; | 84% |
Conditions | Yield |
---|---|
In benzene at 20℃; | 80% |
In diethyl ether at -30℃; | 74% |
With benzene | |
With diethyl ether | |
In tetrahydrofuran; dichloromethane at 20℃; Cooling with ice; |
Conditions | Yield |
---|---|
In benzene Reflux; Schlenk technique; | 63% |
N,N-dimethyl acetamide
Li{(CH2)(CH2)P(C6H5)2}
methyl iodide
A
N,N-dimethyl-propanamide
B
diphenylethylmethylphosphonium iodide
Conditions | Yield |
---|---|
at -50℃; for 5h; 1 equiv. of MeI; | A 60% B 60% |
N,N-Dimethylacrylamide
A
N,N-dimethyl-propanamide
B
bis(N,N-dimethyl)-γ-ketopimelamide
Conditions | Yield |
---|---|
With carbon monoxide; isopropyl alcohol; dodecacarbonyltetrarhodium(0) at 180℃; for 6h; Pressure (range begins): 75 ; | A 31 % Chromat. B 47% |
N,N-Dimethylacrylamide
carbon monoxide
A
N,N-dimethyl-propanamide
B
bis(N,N-dimethyl)-γ-ketopimelamide
Conditions | Yield |
---|---|
With isopropyl alcohol; dodecacarbonyltetrarhodium(0) at 180℃; for 6h; Pressure (range begins): 75 ; | A 31% B 47 % Chromat. |
N,N,N,N,N,N-hexamethylphosphoric triamide
propionic acid
N,N-dimethyl-propanamide
Conditions | Yield |
---|---|
under 100 Torr; |
Conditions | Yield |
---|---|
With air at 155℃; |
N,N,N,N,N,N-hexamethylphosphoric triamide
propionic acid anhydride
N,N-dimethyl-propanamide
Conditions | Yield |
---|---|
at 165℃; |
Conditions | Yield |
---|---|
With water |
Conditions | Yield |
---|---|
(i) NaNH2, liq. NH3, (ii) /BRN= 969135/; Multistep reaction; | |
With triethylgermyllithium 1) THF, -20 deg C, 1 h, 2) THF, -20 deg C to r.t., 0.5 h; Yield given. Multistep reaction; | |
With (triethylgermyl)potassium 1.) THF, -20 deg C, 1 h, 2.) THF, RT, 1 h; Yield given. Multistep reaction; |
N,N-dimethyl acetamide
A
N,N-Dimethylamino acetonitrile
B
N,N-dimethyl-propanamide
C
acetone
Conditions | Yield |
---|---|
under 0.008 - 0.8 Torr; radio-frequency discharge; Yield given. Yields of byproduct given; |
Conditions | Yield |
---|---|
aluminum oxide at 240℃; Kinetics; Rate constant; temperature range 200 - 320 deg C, energy of activation; |
Conditions | Yield |
---|---|
In various solvent(s) at 70 - 90℃; Kinetics; Activation energy; decomplexation; |
W2(CH2CH3)2(N(CH3)2)4
propionic acid anhydride
B
N,N-dimethyl-propanamide
Conditions | Yield |
---|---|
In not given byproducts: C2H4, C2H6; react. hydrocarbon soln. 1,2-W2Et2(NMe2)4 with acid anhydride at room temp.; crystn. from benzene or hexane; |
N,N-dimethyl-propanamide
Conditions | Yield |
---|---|
at 260℃; under 22502.3 Torr; for 0.0125h; Microwave irradiation; |
Conditions | Yield |
---|---|
With sodium tetrahydroborate; iron(III) trifluoromethanesulfonate; ethanol at 20℃; for 6h; Inert atmosphere; Green chemistry; chemoselective reaction; | |
With [Cp(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)Ru(pyridine)2][PF6]; potassium tert-butylate; isopropyl alcohol at 70℃; for 8h; Glovebox; Schlenk technique; Inert atmosphere; | 98 %Spectr. |
Conditions | Yield |
---|---|
With gold at 40℃; under 760.051 Torr; Green chemistry; |
propionic acid
N,N-dimethyl-formamide
N,N-dimethyl-propanamide
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; (p-cymene)ruthenium(II) chloride; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene at 160℃; for 6h; | 93 %Chromat. |
N,O-dimethylhydroxylamine*hydrochloride
propionic acid
N,N-dimethyl-propanamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 0 - 20℃; |
N,N-dimethyl-propanamide
vinyltriphenylsilane
Conditions | Yield |
---|---|
Stage #1: vinyltriphenylsilane With 18-crown-6 ether; potassium hexamethylsilazane at 25℃; for 0.5h; Inert atmosphere; Stage #2: N,N-dimethyl-propanamide at 25℃; for 6h; Catalytic behavior; Reagent/catalyst; Temperature; Inert atmosphere; | 100% |
N,N-dimethyl-propanamide
benzaldehyde
3-hydroxy-2,N,N-trimethyl-3-phenylpropionamide
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-propanamide With n-butyllithium; polymer-bound N-isopropyl-5-(4-vinylphenyl)pentylamine In tetrahydrofuran; hexane at -78 - 20℃; for 0.5h; Stage #2: benzaldehyde In tetrahydrofuran; hexane at -78℃; for 1.5h; Further stages.; | 99% |
(i) nBuLi, <1,3,5>trithiane, THF, (ii) /BRN= 471223/; Multistep reaction; |
N,N-dimethyl-propanamide
1-[chloro(p-tolylsulfinyl)methylidene]cyclobutane
2-(1-[chloro(p-tolylsulfinyl)methyl]cyclobutyl)-N,N-dimethylpropionamide
Conditions | Yield |
---|---|
With lithium diisopropyl amide In tetrahydrofuran at -78℃; for 0.25h; | 99% |
Stage #1: N,N-dimethyl-propanamide With lithium diisopropyl amide In tetrahydrofuran at -78℃; for 0.166667h; Stage #2: 1-[chloro(p-tolylsulfinyl)methylidene]cyclobutane In tetrahydrofuran at -78℃; for 0.25h; Inert atmosphere; Stage #3: With ammonium chloride In tetrahydrofuran; water | 99% |
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-propanamide With trichlorophosphate at 0 - 20℃; for 0.25h; Stage #2: pyrrole In 1,2-dichloro-ethane at 0℃; for 0.5h; Heating / reflux; Stage #3: With sodium acetate In water; 1,2-dichloro-ethane for 0.5h; Heating / reflux; | 98% |
Stage #1: N,N-dimethyl-propanamide With bis(trichloromethyl) carbonate In tetrachloromethane at 0℃; Stage #2: pyrrole In tetrachloromethane at 40 - 50℃; for 1h; Vilsmeier-Haack reaction; Stage #3: With sodium hydroxide In tetrachloromethane | 87% |
With sodium hydroxide; water; trichlorophosphate 1) benzene, 18 h, 20 deg C, 2) 1 h, 20 deg C; Yield given. Multistep reaction; |
N,N-dimethyl-propanamide
dimethylaminobis(trifluoromethyl)borane
1-dimethylaminocarbonylethyl-bis(trifluoromethyl)borane-dimethylamine
Conditions | Yield |
---|---|
In pentane dopwise addn. of (CF3)2BNMe2 to a stirred soln. of the carbonyl compound in dry pentane at 4°C; warmed to room temp. with stirring (1 h);; removal of solvent and volatile by-products in vac. at room temp., purifn. by sublimation in vac.; elem. anal.;; | 98% |
N,N-dimethyl-propanamide
1,3-diphenyl-1H-pyrazol-5-amine
N'-(1,3-diphenyl-1H-pyrazol-5-yl)-N,N-dimethylpropanimidamide
Conditions | Yield |
---|---|
With trichlorophosphate at 30 - 40℃; Microwave irradiation; | 95% |
Conditions | Yield |
---|---|
Stage #1: styrene With 18-crown-6 ether; potassium hexamethylsilazane at 0℃; for 0.5h; Inert atmosphere; Stage #2: N,N-dimethyl-propanamide at 0℃; for 6h; Inert atmosphere; | 95% |
With potassium tert-butylate at 80℃; for 2h; Sealed tube; | 93% |
Conditions | Yield |
---|---|
Stage #1: 1-methyl-2-vinyl-benzene With 18-crown-6 ether; potassium hexamethylsilazane at 25℃; for 0.5h; Inert atmosphere; Stage #2: N,N-dimethyl-propanamide at 25℃; for 9h; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
Stage #1: 1,1-Diphenylethylene With 18-crown-6 ether; potassium hexamethylsilazane at 25℃; for 0.5h; Inert atmosphere; Stage #2: N,N-dimethyl-propanamide at 25℃; for 9h; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
Stage #1: 1-bromo-4-ethenyl-benzene With 18-crown-6 ether; 1,1,1,3,3,3-hexamethyl-disilazane at 25℃; for 0.5h; Inert atmosphere; Stage #2: N,N-dimethyl-propanamide at 25℃; for 6h; Inert atmosphere; | 94% |
N,N-dimethyl-propanamide
N,N-dimethylpropane-1-amine hydrochloride
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-propanamide With [κ2-{Ph2P(Se)NC9H6N}Al(Me)2]; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane at 20℃; for 12h; Schlenk technique; Glovebox; Stage #2: With hydrogenchloride In water chemoselective reaction; | 94% |
Stage #1: N,N-dimethyl-propanamide With bis(cyclopentadienyl)dihydrozirconium; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane at 20℃; under 760.051 Torr; for 12h; Inert atmosphere; Stage #2: With hydrogenchloride In diethyl ether Inert atmosphere; | 87% |
N,N-dimethyl-propanamide
methyl 3-(benzyloxy)benzoate
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-propanamide With lithium diisopropyl amide In tetrahydrofuran at -78℃; for 2h; Inert atmosphere; Stage #2: methyl 3-(benzyloxy)benzoate In tetrahydrofuran at -78 - 20℃; for 12h; Inert atmosphere; | 94% |
Conditions | Yield |
---|---|
With lithium tert-butoxide In tetrahydrofuran at 23℃; for 3h; Glovebox; | 94% |
Conditions | Yield |
---|---|
With Selectfluor at 110℃; for 12h; | 92% |
N,N-dimethyl-propanamide
2-tert-butyldimethylsilyloxyethyl iodide
C13H29NO2Si
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-propanamide With lithium chloride; lithium diisopropyl amide In tetrahydrofuran; hexanes at -78 - 20℃; for 1.33333h; Inert atmosphere; Stage #2: 2-tert-butyldimethylsilyloxyethyl iodide In tetrahydrofuran; hexanes at 0℃; for 3.5h; Inert atmosphere; | 91% |
Stage #1: N,N-dimethyl-propanamide With n-butyllithium; diisopropylamine; lithium chloride In tetrahydrofuran; hexane at -78 - 20℃; Inert atmosphere; Stage #2: 2-tert-butyldimethylsilyloxyethyl iodide In tetrahydrofuran; hexane at 0℃; for 3.5h; Inert atmosphere; | 91% |
phthalimide
N,N-dimethyl-propanamide
N-[(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl]-N-methylpropionamide
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide; potassium iodide In water at 90℃; for 1h; | 91% |
Conditions | Yield |
---|---|
With Selectfluor at 110℃; for 12h; Temperature; Reagent/catalyst; | 91% |
Conditions | Yield |
---|---|
Stage #1: dimethyltitanocene; N,N-dimethyl-propanamide In toluene at 65℃; Schlenk technique; Inert atmosphere; Stage #2: With bromine In toluene at -78℃; for 0.0333333h; Schlenk technique; Inert atmosphere; Stage #3: With water In toluene at 20℃; for 1h; Solvent; Temperature; Reagent/catalyst; Schlenk technique; Inert atmosphere; regioselective reaction; | 90% |
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; potassium iodide at 80℃; for 6h; Schlenk technique; | 90% |
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-propanamide With lithium diisopropyl amide In tetrahydrofuran at -78℃; for 2h; Inert atmosphere; Stage #2: methyl 2-fluorobenzoate In tetrahydrofuran at -78 - 20℃; for 12h; Inert atmosphere; | 90% |
N-Methylpyrrole
N,N-dimethyl-propanamide
1-(1-methyl-1H-pyrrol-2-yl)-1-propanone
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-propanamide With bis(trichloromethyl) carbonate In tetrachloromethane at 0℃; Stage #2: N-Methylpyrrole In tetrachloromethane at 40 - 50℃; for 1h; Vilsmeier-Haack reaction; Stage #3: With sodium hydroxide In tetrachloromethane | 88% |
N,N-dimethyl-propanamide
benzoic acid hydrazide
2-ethyl-5-phenyl-1,3,4-oxadiazole
Conditions | Yield |
---|---|
With trichlorophosphate at 80℃; for 0.666667h; | 88% |
N,N-dimethyl-propanamide
4-chlorobenzamide
N,N'-methylenebis(4-chlorobenzamide)
Conditions | Yield |
---|---|
With Selectfluor at 110℃; for 12h; | 88% |
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-propanamide With lithium diisopropyl amide In tetrahydrofuran at -78℃; for 2h; Inert atmosphere; Stage #2: methyl 4-methoxybenzoate In tetrahydrofuran at -78 - 20℃; for 12h; Inert atmosphere; | 88% |
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-propanamide With lithium diisopropyl amide In tetrahydrofuran at -78℃; for 2h; Inert atmosphere; Stage #2: 1-methoxycarbonyl-3-methylbenzene In tetrahydrofuran at -78 - 20℃; for 12h; Inert atmosphere; | 88% |
N,N-dimethyl-propanamide
anthranilic acid amide
2-ethyl-3H-quinazolin-4-one
Conditions | Yield |
---|---|
With Imidazole hydrochloride at 150℃; for 13h; | 88% |
N,N-dimethyl-propanamide
(Z)-7,7,7-trifluoro-2,2,6-trimethylhept-4-en-3-one
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-propanamide With lithium diisopropyl amide In tetrahydrofuran at -78℃; Stage #2: (Z)-7,7,7-trifluoro-2,2,6-trimethylhept-4-en-3-one In tetrahydrofuran at -78℃; for 2h; Further stages.; | 87.6% |
benzophenone
N,N-dimethyl-propanamide
3,3-diphenyl-2-methyl-3-hydroxy- N,N-dimethylpropionamide
Conditions | Yield |
---|---|
With samarium; copper(l) iodide; iodine at 80℃; for 2h; | 87% |
(i) nBuLi, <1,3,5>trithiane, THF, (ii) /BRN= 1238185/; Multistep reaction; | |
With cerium(III) chloride; lithium diisopropyl amide Yield given. Multistep reaction; |
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