As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch
Cas:556-56-9
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
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
Cas:556-56-9
Min.Order:5 Kiloliter
FOB Price: $1.2 / 5.0
Type:Manufacturers
inquiryProduct Name: ALLYL IODIDE Synonyms: 1-propene,3-iodo-;2-Propene, 1-iodo;2-Propenyliodide;3-iodo-1-propen;3-iodo-prop-1-ene;3-iodo-propen;3-Iodpropen;3-Jod-1-propen CAS: 556-56-9 MF: C3H5I MW: 167.98 EIN
Cas:556-56-9
Min.Order:1 Kilogram
FOB Price: $8900.0
Type:Lab/Research institutions
inquirysuperior quality moderate price & quick delivery Appearance:clear orange, red or red-brown liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Applicat
J&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
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Cas:556-56-9
Min.Order:0
Negotiable
Type:Manufacturers
inquiryProduct Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:556-56-9
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
Cas:556-56-9
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiry1.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
Cas:556-56-9
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiryCompound sourcing ServicesAgency of testing serviceFactory audit serviceFounded in Dec. 1999, Nanjing Chemlin Chemical Industrial Co.,Ltd(CHEMLIN) has been covering the business scope from trading of chemicals to custom-synthesis & Manufacturing. Co
Yinghao Pharm products include: leader molecule, heterocyclic compounds,chiral compounds, photoelectric materials, biochemical reagents etc. For example:benzene, pyrimidine, boricacid,pyridine, pyrazole, imidazole, pyrrole, fluorine and other derivat
in stock Assay:99% white powder dentification(HPLC) :The retention time of the major peak in the chromatogram of the assay preparation corresponds to that in the chromatogram of the Conformal standard preparation, as obtained in the ass
At Share Chemical Company, we scrupulously abide by our policy of “Excellent Quality at a Reasonable Price”. We strive to satisfy all of our customers by providing the finest quality products supported by the finest in customer servi
high quality and competitive priceAppearance:colorless Storage:dry,cool Package:UN drum Application:intermediate Transportation:FOB or CIF
At Capot,We can synthesize and purify your complex molecules from 100 gram to 10 tons.Appearance:Clear colorless to light yellow liquid Storage:Dry,Seal and Cool place Package:1G,5G,10G,25G,100G,250G,500G,1KG,5KG,10KG,25KG,50KG,100KG,150KG,200KG. App
1.We have rich experience in the development and production 2.Our factory is in Shanghai of China,We have convenient traffic conditions.3.We have advanced testing equipment and shipping line. Package:5g, 10g, 50g, 100g, 1kg Application:Pharmaceutical
Adequate stocks available,prompt shipment,Strictly control on quality,Timely after-sales
Cas:556-56-9
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryCFTC?PharmaChem?is?a?service?based?company?in?China,?a?pharmachem?division?of?Changzhou?Foreign?Trade?Corp.,supplying?raw?materials,?intermediates,?APIs?and?fine?chemicals?for?the?pharmaceutical?and?specialty?chemical?industries?worldwide. Applicatio
Has its own laboratory, R & D and production, spot Package:100mg Application:As an auxiliary additive, used as medicine, food fine chemical industry
The interaction of allyl iodide with MoO3, Bi2O3 and molybdates of Bi, Co and Mg has been studied in the temperature range of 270-480C. Package:25, 100 g in glass bottle Application:Allyl iodide has been employed as:precursor for generation of allyl
high purity Application:Drug intermediates Materials intermediates and active molecules
Conditions | Yield |
---|---|
With diphosphorus tetraiodide at 85℃; under 0.01 Torr; for 0.0833333h; Product distribution; various alcohols; other conditions of the reaction; | 86% |
With diphosphorus tetraiodide at 85℃; under 0.01 Torr; for 0.0833333h; | 86% |
With Silphos; iodide In acetonitrile for 0.166667h; Heating; | 78% |
Conditions | Yield |
---|---|
With iodine In chloroform at 25℃; for 4h; | A 80% B 85% |
Conditions | Yield |
---|---|
at 25℃; for 8h; | A n/a B 78% |
allyl bromide
A
allyl iodid
B
3-fluoropropene
C
allyl trifluoromethyl ether
Conditions | Yield |
---|---|
With tertamethylammonium iodide In N,N-dimethyl-formamide at 60℃; for 72h; | A n/a B n/a C 72% |
Conditions | Yield |
---|---|
With 2-chloro-4,6-dimethoxy-1 ,3,5-triazine; sodium iodide In acetone Reflux; | 70% |
allyldiphenyltelluronium bromide
A
allyl iodid
B
dibromo-diphenyl-λ4-tellane
Conditions | Yield |
---|---|
With iodine(I) bromide at 0℃; for 4h; | A n/a B 65% |
C16H17BrOTe
A
allyl iodid
B
dibromo-(4-methoxy-phenyl)-phenyl-λ4-tellane
Conditions | Yield |
---|---|
With iodine(I) bromide at 0℃; for 4h; | A n/a B 65% |
rubidium trifluoromethoxylate
allyl bromide
A
allyl iodid
B
3-fluoropropene
C
allyl trifluoromethyl ether
Conditions | Yield |
---|---|
rubidium iodide In N,N-dimethyl-formamide at 60℃; for 61h; | A n/a B n/a C 61% |
allyl diphenyl phosphate
allyl iodid
Conditions | Yield |
---|---|
With sodium iodide In N,N-dimethyl-formamide for 3h; Ambient temperature; | 47% |
2-propenyl nitrate
allyl iodid
Conditions | Yield |
---|---|
With acetone; sodium iodide |
Conditions | Yield |
---|---|
With hydrogen iodide; zinc |
Conditions | Yield |
---|---|
With triphenyl phosphite |
Conditions | Yield |
---|---|
With diphosphorus tetraiodide |
Conditions | Yield |
---|---|
With diphosphorus tetraiodide | |
With iodine | |
With phosphorous; iodine | |
With phosphorus; iodine | |
With phosphorus; iodine Darst.; |
Conditions | Yield |
---|---|
With pyridine; tributyltin iodide at 50℃; Thermodynamic data; Equilibrium constant; Δ G; | |
With acetone; sodium iodide | |
With methyl iodide; aluminum oxide; tetrabutyl phosphonium bromide at 170℃; | 75 % Spectr. |
With sodium iodide In acetone |
allyl radical
allyl iodid
Conditions | Yield |
---|---|
With I at 22.9℃; Rate constant; |
Conditions | Yield |
---|---|
With n-butyllithium; zirconocene dichloride; iodine 1.) from -78 deg C to 0 deg C; Multistep reaction; |
Conditions | Yield |
---|---|
With tetrabutylammomium bromide In nitromethane-d3 at 25℃; Equilibrium constant; Thermodynamic data; ΔG; |
Conditions | Yield |
---|---|
With hydrogenchloride; sodium iodide at 60℃; electrochemical reduction, Hg-cathode; |
(diethoxyphosphinyl)methyl trifluoromethanesulfonate
allyl bromide
A
allyl iodid
Conditions | Yield |
---|---|
With sodium iodide In acetone |
Conditions | Yield |
---|---|
With pyridine; tributyltin iodide at 50℃; Thermodynamic data; Equilibrium constant; Δ G; | |
With iodine; iron pentacarbonyl at 75 - 80℃; for 0.25h; further reagent; Yield given; | |
With sodium iodide In acetone at 22℃; for 1h; | |
With sodium iodide In acetone at 20℃; Inert atmosphere; Darkness; |
allyl iodid
Conditions | Yield |
---|---|
In chloroform Heating; sealed tube; | |
In solid Rate constant; Heating; sealed tube; |
A
allyl iodid
B
eschenmoser's salt
Conditions | Yield |
---|---|
In [D3]acetonitrile at 40℃; Activation energy; Kinetics; Further Variations:; Temperatures; Decomposition; |
hydrogen iodide
glycerol
A
2-iodo-propane
B
propene
C
allyl iodid
sodium allyloxide
diallyl phosphite
allyl alcohol
A
allyl iodid
B
diallyl allylphosphonate
Conditions | Yield |
---|---|
beim anschliessenden Erwaermen mit Dijodmethan; |
N-allyl-1,2-phenylenediamine
A
allyl iodid
Conditions | Yield |
---|---|
at 73 - 135℃; thermal decomposition; |
Conditions | Yield |
---|---|
With hydrogen at 120℃; under 1 Torr; |
allyl iodid
(S)-4-benzyl-3-butyryloxazolidin-2-one
(S)-3-<(R)-2-ethyl-1-oxo-4-penten-1-yl>-4-(phenylmethyl)-1,3-oxazolidin-2-one
Conditions | Yield |
---|---|
With sodium hexamethyldisilazane at -78℃; optical yield given as %de; | 100% |
Stage #1: (S)-4-benzyl-3-butyryloxazolidin-2-one With lithium diisopropyl amide In tetrahydrofuran at -78℃; for 0.5h; Stage #2: allyl iodid In tetrahydrofuran at -78 - 20℃; | 67% |
Stage #1: (S)-4-benzyl-3-butyryloxazolidin-2-one With sodium hexamethyldisilazane In tetrahydrofuran at -78℃; Stage #2: allyl iodid In tetrahydrofuran at -78℃; for 18h; | 62% |
With sodium hexamethyldisilazane 1) THF, -78 - -70 deg C, 30 min, 2) -78 deg C, 3 h; Yield given. Multistep reaction; |
allyl iodid
(-)-phenylmenthyl half ester of ethylmalonic acid
(1R,3R,4S)-8-phenyl-p-menthan-3-yl hydrogen allyl(ethyl)malonate
Conditions | Yield |
---|---|
With lithium diisopropyl amide In tetrahydrofuran at -78 - -50℃; for 3h; Mechanism; | 100% |
With lithium diisopropyl amide 2.) THF, from -78 to -50 deg C, 3 h; Yield given. Multistep reaction; |
allyl iodid
Conditions | Yield |
---|---|
In [D3]acetonitrile for 0.0833333h; | 100% |
Conditions | Yield |
---|---|
With antimony In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide for 15h; Heating; | 100% |
With water; tin(ll) chloride at 50℃; for 12h; Barbier reaction; | 98% |
With stannous fluoride In various solvent(s) for 1h; Ambient temperature; | 96% |
allyl iodid
(Z)-2-phenyl-1-trimethylsilylethenenethiol
Conditions | Yield |
---|---|
With potassium carbonate In acetone Ambient temperature; | 100% |
allyl iodid
Conditions | Yield |
---|---|
With samarium diiodide In various solvent(s) at -78℃; for 2h; | 100% |
allyl iodid
Conditions | Yield |
---|---|
With samarium diiodide In various solvent(s) at -78℃; for 2h; | 100% |
allyl iodid
5,8-dimethoxy-4-methylquinolin-2(1H)-one
4-But-3-enyl-5,8-dimethoxy-1H-quinolin-2-one
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran at -78 - 20℃; for 14h; | 100% |
allyl iodid
Conditions | Yield |
---|---|
With cesium hydroxide; Br(1-)*C60H44F4N(1+) In toluene at -10℃; for 24h; Inert atmosphere; optical yield given as %ee; enantioselective reaction; | 100% |
allyl iodid
5-hydroxy-1-(pyrrolidin-1-yl)pentan-1-one
5-allyloxy-1-(pyrrolidin-1-yl)pentan-1-one
Conditions | Yield |
---|---|
Stage #1: 5-hydroxy-1-(pyrrolidin-1-yl)pentan-1-one With sodium hydride In tetrahydrofuran; mineral oil at 0℃; Inert atmosphere; Stage #2: allyl iodid In tetrahydrofuran; mineral oil at 0 - 20℃; Inert atmosphere; | 100% |
allyl iodid
1-tert-butyl 4-ethyl piperidine-1,4-dicarboxylate
1-(1,1-dimethylethyl) 4-ethyl 4-(2-propenyl)-1,4-piperidinedicarboxylate
Conditions | Yield |
---|---|
Stage #1: 1-tert-butyl 4-ethyl piperidine-1,4-dicarboxylate With n-butyllithium; diisopropylamine In tetrahydrofuran; hexane at -78℃; for 0.75h; Stage #2: allyl iodid With N,N,N,N,N,N-hexamethylphosphoric triamide In tetrahydrofuran; hexane at -78 - 0℃; for 1h; | 100% |
Stage #1: 1-tert-butyl 4-ethyl piperidine-1,4-dicarboxylate With n-butyllithium; diisopropylamine In tetrahydrofuran; hexane at -78℃; for 0.75h; Stage #2: allyl iodid With N,N,N,N,N,N-hexamethylphosphoric triamide In tetrahydrofuran; hexane at -78 - 20℃; for 1h; | 100% |
allyl iodid
(S)-4-[(R,E)-1-(t-butyldimethylsilyloxy)but-2-enyl]oxazolidin-2-one
(S)-3-allyl-4-[(R,E)-1-(t-butyldimethylsilyloxy)but-2-enyl]oxazolidin-2-one
Conditions | Yield |
---|---|
Stage #1: (S)-4-[(R,E)-1-(t-butyldimethylsilyloxy)but-2-enyl]oxazolidin-2-one With sodium hydride In 1,2-dichloro-ethane at 0℃; for 1h; Inert atmosphere; Stage #2: allyl iodid In 1,2-dichloro-ethane at 0℃; Reflux; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
at 65℃; for 2h; Neat (no solvent); | 100% |
allyl iodid
2-(t-butyl-dimethylsilyl)amino-4-chloro-7-methyl-pyrrolo[2,3-d]pyrimidine
2-(prop-2-en-1-yl)amino-4-chloro-7-methyl-pyrrolo[2,3-d]pyrimidine
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0℃; for 0.5h; Inert atmosphere; | 100% |
allyl iodid
Conditions | Yield |
---|---|
Stage #1: 4-benzyl-5-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methylmorpholin-3-one With lithium hexamethyldisilazane In tetrahydrofuran at -78℃; for 0.25h; Stage #2: allyl iodid In tetrahydrofuran at 20℃; | 100% |
Stage #1: 4-benzyl-5-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methylmorpholin-3-one With lithium hexamethyldisilazane In tetrahydrofuran at -78℃; for 0.25h; Inert atmosphere; Stage #2: allyl iodid In tetrahydrofuran at -78 - 20℃; Inert atmosphere; | |
Stage #1: 4-benzyl-5-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methylmorpholin-3-one With lithium hexamethyldisilazane In tetrahydrofuran at -78℃; for 0.25h; Inert atmosphere; Stage #2: allyl iodid In tetrahydrofuran at -78 - 20℃; Inert atmosphere; |
allyl iodid
Conditions | Yield |
---|---|
Stage #1: methyl 3-((1R,2R)-2-(1-methyl-1H-1,2,3-triazol-4-yl)cyclopropyl)-3-oxopropanoate With sodium t-butanolate In tetrahydrofuran; acetonitrile at -40℃; for 0.5h; Stage #2: allyl iodid In tetrahydrofuran at 20℃; for 0.833333h; | 100% |
Conditions | Yield |
---|---|
In ethanol at 82℃; for 24h; | 100% |
Conditions | Yield |
---|---|
In ethanol at 82℃; for 24h; | 100% |
Conditions | Yield |
---|---|
In ethanol at 82℃; for 24h; | 100% |
Conditions | Yield |
---|---|
In ethanol at 82℃; for 24h; | 100% |
Conditions | Yield |
---|---|
In acetonitrile for 24h; Reflux; | 100% |
allyl iodid
2-(4-chlorophenyl)-1-[4-(methylthio)phenyl]-1-ethanone
Conditions | Yield |
---|---|
Stage #1: 2-(4-chlorophenyl)-1-[4-(methylthio)phenyl]-1-ethanone With lithium diisopropyl amide In tetrahydrofuran at -20 - 0℃; for 0.333333h; Stage #2: allyl iodid In tetrahydrofuran at -20 - 0℃; for 0.5h; | 99.8% |
Conditions | Yield |
---|---|
With bismuth(III) chloride; iron In tetrahydrofuran for 4.5h; Ambient temperature; | 99% |
With bismuth(III) chloride; iron In tetrahydrofuran | 99% |
antimony(III) chloride; iron In N,N-dimethyl-formamide at 25℃; for 20h; Product distribution; allyl bromide, NaI; SbCl3,Al; DMF- water; further substituted benzene aldehydes, heptaldehyde, cinnamaldehyde; | 98% |
allyl iodid
N,N-dimethyl-aniline
N-allyl-N,N-dimethylbenzenaminium iodide
Conditions | Yield |
---|---|
at 30℃; | 99% |
Conditions | Yield |
---|---|
With cadmium In N,N-dimethyl-formamide for 1.5h; Ambient temperature; | 99% |
allyl iodid
3-methyl-4-nitrophenol
4-(allyloxy)-2-methyl-1-nitrobenzene
Conditions | Yield |
---|---|
With caesium carbonate In acetone for 24h; Ambient temperature; | 99% |
allyl iodid
5-Hydroxy-1-methoxy-5-<3-(tetrahydropyran-2-yloxy)butynyl>benzocyclobuten-6-one
1-Methoxy-5-(2-propenyloxy)-5-<3-(tetrahydropyran-2-yloxy)butyn-1-yl>benzocyclobuten-6-one
Conditions | Yield |
---|---|
With silver carbonate In 1,4-dioxane | 99% |
Conditions | Yield |
---|---|
antimony(III) chloride; iron In N,N-dimethyl-formamide at 25℃; for 24h; | 99% |
With antimony(III) chloride; iron In N,N-dimethyl-formamide at 25℃; for 24h; | 99% |
With indium In N,N-dimethyl-formamide for 1h; Ambient temperature; | 98% |
With indium iodide In tetrahydrofuran for 1h; Ambient temperature; | 96% |
With cadmium In N,N-dimethyl-formamide for 1.5h; Ambient temperature; | 74% |
allyl iodid
methyl 6-deoxy-6-(p-tolylthio)-2,3,4-tri-O-benzyl-α-D-glucopyranoside
Conditions | Yield |
---|---|
With silver perchlorate In acetonitrile for 48h; Ambient temperature; | 99% |
allyl iodid
3-Fluorobenzaldehyde
(+/-)-1-(3'-fluorophenyl)but-3-en-1-ol
Conditions | Yield |
---|---|
With indium In water for 48h; | 99% |
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