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Dayang Chem (Hangzhou) Co.,Ltd.

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

3-Iodopropene

Cas:556-56-9

Min.Order:1 Kilogram

FOB Price: $3.0

Type:Lab/Research institutions

inquiry

Chemwill Asia Co., Ltd.

Our 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

3-Iodo-1-propene

Cas:556-56-9

Min.Order:5 Kiloliter

FOB Price: $1.2 / 5.0

Type:Manufacturers

inquiry

Henan Tianfu Chemical Co., Ltd.

Product 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

556-56-9 ALLYL IODIDE

Cas:556-56-9

Min.Order:1 Kilogram

FOB Price: $8900.0

Type:Lab/Research institutions

inquiry

HANGZHOU YUNUO CHEMICAL CO.,LTD

superior 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

3-iodopropene

Cas:556-56-9

Min.Order:1 Kilogram

Negotiable

Type:Trading Company

inquiry

Hangzhou J&H Chemical Co., Ltd.

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

1-Propene, 3-iodo-

Cas:556-56-9

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Kono Chem Co.,Ltd

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

3-iodopropene

Cas:556-56-9

Min.Order:0

Negotiable

Type:Other

inquiry

Henan Allgreen Chemical Co.,Ltd

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

Allyl iodide, 97+ %, stab. with copper

Cas:556-56-9

Min.Order:0

Negotiable

Type:Manufacturers

inquiry

Zhuozhou Wenxi import and Export Co., Ltd

Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard

factory supply CAS 556-56-9 with competitive price

Cas:556-56-9

Min.Order:1 Kilogram

FOB Price: $112.0

Type:Trading Company

inquiry

Antimex Chemical Limied

Ansciep 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

Allyl Iodide (stabilized with Copper chip)

Cas:556-56-9

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Amadis Chemical Co., Ltd.

1.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

Amadis Chemical offer CAS#556-56-9;CAT#A830736

Cas:556-56-9

Min.Order:10 Milligram

Negotiable

Type:Lab/Research institutions

inquiry

HENAN SUNLAKE ENTERPRISE CORPORATION

ALLYL IODIDE Basic information Product Name: ALLYL IODIDE S

556-56-9 C3H5I ALLYL IODIDE

Cas:556-56-9

Min.Order:100 Gram

Negotiable

Type:Trading Company

inquiry

Nanjing Chemlin Chemical Co., Ltd.

Compound 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

556-56-9

Cas:556-56-9

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Yinghao Pharm Co.,Ltd.

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

ALLYL IODIDE

Cas:556-56-9

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

WUHAN YING YUAN BEI TECHNOLOGY CO., LTD

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

ALLYL IODIDE

Cas:556-56-9

Min.Order:1 Kilogram

FOB Price: $10.0

Type:Trading Company

inquiry

Hangzhou Share Chemical Co., Ltd

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

Allyl iodide, 97+%, stab. with c

Cas:556-56-9

Min.Order:1 Gram

Negotiable

Type:Other

inquiry

Zouping Mingxing Chemical Co.,Ltd.

high quality and competitive priceAppearance:colorless Storage:dry,cool Package:UN drum Application:intermediate Transportation:FOB or CIF

3-Iodopropene

Cas:556-56-9

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Capot Chemical Co., Ltd.

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

Allyl iodide

Cas:556-56-9

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Shanghai Run-Biotech Co., Ltd.

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

3-Iodo-1-propene

Cas:556-56-9

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Skyrun Industrial Co.,Ltd

Adequate stocks available,prompt shipment,Strictly control on quality,Timely after-sales

Allyl iodide, 97+%, stab. with copper

Cas:556-56-9

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Shanghai chamflyer chemicals Co., Ltd

High quality Application:Pharmaceutial

3-Iodo-1-propene

Cas:556-56-9

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Changzhou Foreign Trade Corp

CFTC?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

3-iodopropene

Cas:556-56-9

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Beijing Jin Ming Biotechnology Co., Ltd.

Has its own laboratory, R & D and production, spot Package:100mg Application:As an auxiliary additive, used as medicine, food fine chemical industry

Allyl Iodide

Cas:556-56-9

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Sigma-Aldrich Chemie GmbH

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

Allyl iodide

Cas:556-56-9

Min.Order:0

Negotiable

Type:Trading Company

inquiry

NovaChemistry

high purity Application:Drug intermediates Materials intermediates and active molecules

3-iodoprop-1-ene

Cas:556-56-9

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Synthetic route

allyl alcohol
107-18-6

allyl alcohol

allyl iodid
556-56-9

allyl iodid

Conditions
ConditionsYield
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%
allyldiphenyltelluronium bromide
76065-43-5

allyldiphenyltelluronium bromide

A

allyl iodid
556-56-9

allyl iodid

B

Ph2TlBr
69007-28-9

Ph2TlBr

Conditions
ConditionsYield
With iodine In chloroform at 25℃; for 4h;A 80%
B 85%
cyanogen iodide
506-78-5

cyanogen iodide

C17H19BrO2Te
76065-47-9

C17H19BrO2Te

A

allyl iodid
556-56-9

allyl iodid

B

C15H14BrNO2Te
76065-56-0

C15H14BrNO2Te

Conditions
ConditionsYield
at 25℃; for 8h;A n/a
B 78%
allyl bromide
106-95-6

allyl bromide

tetramethylammonium trifluoromethoxide

tetramethylammonium trifluoromethoxide

A

allyl iodid
556-56-9

allyl iodid

B

3-fluoropropene
818-92-8

3-fluoropropene

C

allyl trifluoromethyl ether
140899-21-4

allyl trifluoromethyl ether

Conditions
ConditionsYield
With tertamethylammonium iodide In N,N-dimethyl-formamide at 60℃; for 72h;A n/a
B n/a
C 72%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

allyl iodid
556-56-9

allyl iodid

Conditions
ConditionsYield
With 2-chloro-4,6-dimethoxy-1 ,3,5-triazine; sodium iodide In acetone Reflux;70%
allyldiphenyltelluronium bromide
76065-43-5

allyldiphenyltelluronium bromide

A

allyl iodid
556-56-9

allyl iodid

B

dibromo-diphenyl-λ4-tellane
29135-65-7

dibromo-diphenyl-λ4-tellane

Conditions
ConditionsYield
With iodine(I) bromide at 0℃; for 4h;A n/a
B 65%
C16H17BrOTe
76065-53-7

C16H17BrOTe

A

allyl iodid
556-56-9

allyl iodid

B

dibromo-(4-methoxy-phenyl)-phenyl-λ4-tellane
76065-57-1

dibromo-(4-methoxy-phenyl)-phenyl-λ4-tellane

Conditions
ConditionsYield
With iodine(I) bromide at 0℃; for 4h;A n/a
B 65%
rubidium trifluoromethoxylate
2700-81-4

rubidium trifluoromethoxylate

allyl bromide
106-95-6

allyl bromide

A

allyl iodid
556-56-9

allyl iodid

B

3-fluoropropene
818-92-8

3-fluoropropene

C

allyl trifluoromethyl ether
140899-21-4

allyl trifluoromethyl ether

Conditions
ConditionsYield
rubidium iodide In N,N-dimethyl-formamide at 60℃; for 61h;A n/a
B n/a
C 61%
allyl diphenyl phosphate
19206-69-0

allyl diphenyl phosphate

allyl iodid
556-56-9

allyl iodid

Conditions
ConditionsYield
With sodium iodide In N,N-dimethyl-formamide for 3h; Ambient temperature;47%
2-propenyl nitrate
16770-74-4

2-propenyl nitrate

allyl iodid
556-56-9

allyl iodid

Conditions
ConditionsYield
With acetone; sodium iodide
3-formyloxy-propene
1838-59-1

3-formyloxy-propene

allyl iodid
556-56-9

allyl iodid

Conditions
ConditionsYield
With hydrogen iodide; zinc
allyl alcohol
107-18-6

allyl alcohol

methyl iodide
74-88-4

methyl iodide

allyl iodid
556-56-9

allyl iodid

Conditions
ConditionsYield
With triphenyl phosphite
glycerol
56-81-5

glycerol

A

propene
187737-37-7

propene

B

allyl iodid
556-56-9

allyl iodid

Conditions
ConditionsYield
With diphosphorus tetraiodide
glycerol
56-81-5

glycerol

allyl iodid
556-56-9

allyl iodid

Conditions
ConditionsYield
With diphosphorus tetraiodide
With iodine
With phosphorous; iodine
With phosphorus; iodine
With phosphorus; iodine Darst.;
3-chloroprop-1-ene
107-05-1

3-chloroprop-1-ene

allyl iodid
556-56-9

allyl iodid

Conditions
ConditionsYield
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
1981-80-2, 13932-24-6

allyl radical

allyl iodid
556-56-9

allyl iodid

Conditions
ConditionsYield
With I at 22.9℃; Rate constant;
Allyl ether
557-40-4

Allyl ether

A

allyl iodid
556-56-9

allyl iodid

B

allyl alcohol
107-18-6

allyl alcohol

Conditions
ConditionsYield
With n-butyllithium; zirconocene dichloride; iodine 1.) from -78 deg C to 0 deg C; Multistep reaction;
ethyl iodide
75-03-6

ethyl iodide

allyl bromide
106-95-6

allyl bromide

A

ethyl bromide
74-96-4

ethyl bromide

B

allyl iodid
556-56-9

allyl iodid

Conditions
ConditionsYield
With tetrabutylammomium bromide In nitromethane-d3 at 25℃; Equilibrium constant; Thermodynamic data; ΔG;
allyl alcohol
107-18-6

allyl alcohol

A

propene
187737-37-7

propene

B

allyl iodid
556-56-9

allyl iodid

C

1-iodo-propane
107-08-4

1-iodo-propane

Conditions
ConditionsYield
With hydrogenchloride; sodium iodide at 60℃; electrochemical reduction, Hg-cathode;
(diethoxyphosphinyl)methyl trifluoromethanesulfonate
106938-62-9

(diethoxyphosphinyl)methyl trifluoromethanesulfonate

allyl bromide
106-95-6

allyl bromide

A

allyl iodid
556-56-9

allyl iodid

B

diethyl iodomethylphosphonate

diethyl iodomethylphosphonate

Conditions
ConditionsYield
With sodium iodide In acetone
allyl bromide
106-95-6

allyl bromide

allyl iodid
556-56-9

allyl iodid

Conditions
ConditionsYield
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;
Prop-2-ene-1-sulfonyl iodide

Prop-2-ene-1-sulfonyl iodide

allyl iodid
556-56-9

allyl iodid

Conditions
ConditionsYield
In chloroform Heating; sealed tube;
In solid Rate constant; Heating; sealed tube;
1-iodo-N-allyl-N,N-dimethylmethaniminium iodide

1-iodo-N-allyl-N,N-dimethylmethaniminium iodide

A

allyl iodid
556-56-9

allyl iodid

B

eschenmoser's salt
33797-51-2

eschenmoser's salt

Conditions
ConditionsYield
In [D3]acetonitrile at 40℃; Activation energy; Kinetics; Further Variations:; Temperatures; Decomposition;
iodine
7553-56-2

iodine

glycerol
56-81-5

glycerol

aluminium

aluminium

allyl iodid
556-56-9

allyl iodid

glycerol
56-81-5

glycerol

iodophosphorus

iodophosphorus

A

propene
187737-37-7

propene

B

allyl iodid
556-56-9

allyl iodid

hydrogen iodide
10034-85-2

hydrogen iodide

glycerol
56-81-5

glycerol

A

2-iodo-propane
75-30-9

2-iodo-propane

B

propene
187737-37-7

propene

C

allyl iodid
556-56-9

allyl iodid

sodium allyloxide
20907-32-8

sodium allyloxide

diallyl phosphite
23679-20-1

diallyl phosphite

allyl alcohol
107-18-6

allyl alcohol

A

allyl iodid
556-56-9

allyl iodid

B

diallyl allylphosphonate
3479-30-9

diallyl allylphosphonate

C

disodium-salt of methanediyldiphosphonic acid-1,2-diallyl ester

disodium-salt of methanediyldiphosphonic acid-1,2-diallyl ester

Conditions
ConditionsYield
beim anschliessenden Erwaermen mit Dijodmethan;
N-allyl-1,2-phenylenediamine
55899-43-9

N-allyl-1,2-phenylenediamine

A

allyl iodid
556-56-9

allyl iodid

B

1-Allyl-2-pentafluoroethyl-1H-benzoimidazole

1-Allyl-2-pentafluoroethyl-1H-benzoimidazole

C

I2

I2

Conditions
ConditionsYield
at 73 - 135℃; thermal decomposition;
allylmercury iodide

allylmercury iodide

A

allyl iodid
556-56-9

allyl iodid

B

1,5-Hexadien
592-42-7

1,5-Hexadien

Conditions
ConditionsYield
With hydrogen at 120℃; under 1 Torr;
allyl iodid
556-56-9

allyl iodid

(S)-4-benzyl-3-butyryloxazolidin-2-one
111292-87-6, 143097-11-4, 112459-79-7

(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
130710-56-4

(S)-3-<(R)-2-ethyl-1-oxo-4-penten-1-yl>-4-(phenylmethyl)-1,3-oxazolidin-2-one

Conditions
ConditionsYield
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
556-56-9

allyl iodid

(-)-phenylmenthyl half ester of ethylmalonic acid
123463-89-8, 134279-37-1, 134279-38-2

(-)-phenylmenthyl half ester of ethylmalonic acid

(1R,3R,4S)-8-phenyl-p-menthan-3-yl hydrogen allyl(ethyl)malonate
132143-19-2, 132143-25-0

(1R,3R,4S)-8-phenyl-p-menthan-3-yl hydrogen allyl(ethyl)malonate

Conditions
ConditionsYield
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
556-56-9

allyl iodid

C10H21N4PS2

C10H21N4PS2

1-Allylsulfanylthiocarbonyl-2,8,9-trimethyl-2,5,8,9-tetraaza-1-phosphonia-bicyclo[3.3.3]undecane; iodide

1-Allylsulfanylthiocarbonyl-2,8,9-trimethyl-2,5,8,9-tetraaza-1-phosphonia-bicyclo[3.3.3]undecane; iodide

Conditions
ConditionsYield
In [D3]acetonitrile for 0.0833333h;100%
allyl iodid
556-56-9

allyl iodid

4-chlorobenzaldehyde
104-88-1

4-chlorobenzaldehyde

1-(4-chlorophenyl)but-3-en-1-ol
14506-33-3

1-(4-chlorophenyl)but-3-en-1-ol

Conditions
ConditionsYield
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
556-56-9

allyl iodid

(Z)-2-phenyl-1-trimethylsilylethenenethiol
185844-35-3

(Z)-2-phenyl-1-trimethylsilylethenenethiol

((Z)-1-Allylsulfanyl-2-phenyl-vinyl)-trimethyl-silane

((Z)-1-Allylsulfanyl-2-phenyl-vinyl)-trimethyl-silane

Conditions
ConditionsYield
With potassium carbonate In acetone Ambient temperature;100%
allyl iodid
556-56-9

allyl iodid

2-Oxo-propionic acid (S)-2-hydroxy-1,2,2-triphenyl-ethyl ester

2-Oxo-propionic acid (S)-2-hydroxy-1,2,2-triphenyl-ethyl ester

2-Hydroxy-2-methyl-pent-4-enoic acid (S)-2-hydroxy-1,2,2-triphenyl-ethyl ester

2-Hydroxy-2-methyl-pent-4-enoic acid (S)-2-hydroxy-1,2,2-triphenyl-ethyl ester

Conditions
ConditionsYield
With samarium diiodide In various solvent(s) at -78℃; for 2h;100%
allyl iodid
556-56-9

allyl iodid

Oxo-phenyl-acetic acid (S)-2-hydroxy-1,2,2-triphenyl-ethyl ester

Oxo-phenyl-acetic acid (S)-2-hydroxy-1,2,2-triphenyl-ethyl ester

2-Hydroxy-2-phenyl-pent-4-enoic acid (S)-2-hydroxy-1,2,2-triphenyl-ethyl ester

2-Hydroxy-2-phenyl-pent-4-enoic acid (S)-2-hydroxy-1,2,2-triphenyl-ethyl ester

Conditions
ConditionsYield
With samarium diiodide In various solvent(s) at -78℃; for 2h;100%
allyl iodid
556-56-9

allyl iodid

5,8-dimethoxy-4-methylquinolin-2(1H)-one
23947-41-3

5,8-dimethoxy-4-methylquinolin-2(1H)-one

4-But-3-enyl-5,8-dimethoxy-1H-quinolin-2-one
204978-04-1

4-But-3-enyl-5,8-dimethoxy-1H-quinolin-2-one

Conditions
ConditionsYield
With n-butyllithium In tetrahydrofuran at -78 - 20℃; for 14h;100%
tert-butyl (2-bromophenyl)cyanoacetate

tert-butyl (2-bromophenyl)cyanoacetate

allyl iodid
556-56-9

allyl iodid

(R)-tert-butyl 2-(2-bromophenyl)-2-cyanopent-4-enoate

(R)-tert-butyl 2-(2-bromophenyl)-2-cyanopent-4-enoate

Conditions
ConditionsYield
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
556-56-9

allyl iodid

5-hydroxy-1-(pyrrolidin-1-yl)pentan-1-one
73200-35-8

5-hydroxy-1-(pyrrolidin-1-yl)pentan-1-one

5-allyloxy-1-(pyrrolidin-1-yl)pentan-1-one
1221896-00-9

5-allyloxy-1-(pyrrolidin-1-yl)pentan-1-one

Conditions
ConditionsYield
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
556-56-9

allyl iodid

1-tert-butyl 4-ethyl piperidine-1,4-dicarboxylate
142851-03-4

1-tert-butyl 4-ethyl piperidine-1,4-dicarboxylate

1-(1,1-dimethylethyl) 4-ethyl 4-(2-propenyl)-1,4-piperidinedicarboxylate
146603-99-8

1-(1,1-dimethylethyl) 4-ethyl 4-(2-propenyl)-1,4-piperidinedicarboxylate

Conditions
ConditionsYield
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
556-56-9

allyl iodid

(S)-4-[(R,E)-1-(t-butyldimethylsilyloxy)but-2-enyl]oxazolidin-2-one
837375-05-0

(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
1278522-12-5

(S)-3-allyl-4-[(R,E)-1-(t-butyldimethylsilyloxy)but-2-enyl]oxazolidin-2-one

Conditions
ConditionsYield
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%
4-(1-piperidinylmethyl)-1,3-dioxolan-2-one
103117-97-1

4-(1-piperidinylmethyl)-1,3-dioxolan-2-one

allyl iodid
556-56-9

allyl iodid

C12H20NO3(1+)*I(1-)

C12H20NO3(1+)*I(1-)

Conditions
ConditionsYield
at 65℃; for 2h; Neat (no solvent);100%
allyl iodid
556-56-9

allyl iodid

2-(t-butyl-dimethylsilyl)amino-4-chloro-7-methyl-pyrrolo[2,3-d]pyrimidine
134798-58-6

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
134798-56-4

2-(prop-2-en-1-yl)amino-4-chloro-7-methyl-pyrrolo[2,3-d]pyrimidine

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0℃; for 0.5h; Inert atmosphere;100%
allyl iodid
556-56-9

allyl iodid

4-benzyl-5-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methylmorpholin-3-one

4-benzyl-5-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methylmorpholin-3-one

2-allyl-4-phenylmethyl-5-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methyl-morpholin-3-one

2-allyl-4-phenylmethyl-5-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methyl-morpholin-3-one

Conditions
ConditionsYield
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
556-56-9

allyl iodid

methyl 3-((1R,2R)-2-(1-methyl-1H-1,2,3-triazol-4-yl)cyclopropyl)-3-oxopropanoate

methyl 3-((1R,2R)-2-(1-methyl-1H-1,2,3-triazol-4-yl)cyclopropyl)-3-oxopropanoate

methyl 2-((1R,2R)-2-(1-methyl-1H-1,2,3-triazol-4-yl)cyclopropane-1-carbonyl)pent-4-enoate

methyl 2-((1R,2R)-2-(1-methyl-1H-1,2,3-triazol-4-yl)cyclopropane-1-carbonyl)pent-4-enoate

Conditions
ConditionsYield
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%
allyl iodid
556-56-9

allyl iodid

N,N-dimethylbutylamine
927-62-8

N,N-dimethylbutylamine

N-allyl-N,N-dimethyl-N-butylammonium iodide

N-allyl-N,N-dimethyl-N-butylammonium iodide

Conditions
ConditionsYield
In ethanol at 82℃; for 24h;100%
allyl iodid
556-56-9

allyl iodid

tributyl-amine
102-82-9

tributyl-amine

N-allyl-N,N,N-tributylammonium iodide

N-allyl-N,N,N-tributylammonium iodide

Conditions
ConditionsYield
In ethanol at 82℃; for 24h;100%
allyl iodid
556-56-9

allyl iodid

tri-n-hexylamine
102-86-3

tri-n-hexylamine

N-allyl-N,N,N-trihexylammonium iodide

N-allyl-N,N,N-trihexylammonium iodide

Conditions
ConditionsYield
In ethanol at 82℃; for 24h;100%
pyridine
110-86-1

pyridine

allyl iodid
556-56-9

allyl iodid

N-allylpyridinium iodide
26011-64-3

N-allylpyridinium iodide

Conditions
ConditionsYield
In ethanol at 82℃; for 24h;100%
allyl iodid
556-56-9

allyl iodid

Triallylamine
102-70-5

Triallylamine

tetraallylammonium iodide

tetraallylammonium iodide

Conditions
ConditionsYield
In acetonitrile for 24h; Reflux;100%
allyl iodid
556-56-9

allyl iodid

2-(4-chlorophenyl)-1-[4-(methylthio)phenyl]-1-ethanone
225668-35-9

2-(4-chlorophenyl)-1-[4-(methylthio)phenyl]-1-ethanone

2-(4-chlorophenyl)-1-[4-(methylthio)phenyl]-4-penten-1-one

2-(4-chlorophenyl)-1-[4-(methylthio)phenyl]-4-penten-1-one

Conditions
ConditionsYield
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%
allyl iodid
556-56-9

allyl iodid

benzaldehyde
100-52-7

benzaldehyde

1-Phenyl-3-buten-1-ol
80735-94-0

1-Phenyl-3-buten-1-ol

Conditions
ConditionsYield
With bismuth(III) chloride; iron In tetrahydrofuran for 4.5h; Ambient temperature;99%
With bismuth(III) chloride; iron In tetrahydrofuran99%
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
556-56-9

allyl iodid

N,N-dimethyl-aniline
121-69-7

N,N-dimethyl-aniline

N-allyl-N,N-dimethylbenzenaminium iodide
73680-59-8

N-allyl-N,N-dimethylbenzenaminium iodide

Conditions
ConditionsYield
at 30℃;99%
allyl iodid
556-56-9

allyl iodid

(E/Z)-3,7-dimethyl-2,6-octadienal
5392-40-5

(E/Z)-3,7-dimethyl-2,6-octadienal

6,10-dimethylundeca-1,5,9-trien-4-one

6,10-dimethylundeca-1,5,9-trien-4-one

Conditions
ConditionsYield
With cadmium In N,N-dimethyl-formamide for 1.5h; Ambient temperature;99%
allyl iodid
556-56-9

allyl iodid

3-methyl-4-nitrophenol
2581-34-2

3-methyl-4-nitrophenol

4-(allyloxy)-2-methyl-1-nitrobenzene
120106-18-5

4-(allyloxy)-2-methyl-1-nitrobenzene

Conditions
ConditionsYield
With caesium carbonate In acetone for 24h; Ambient temperature;99%
allyl iodid
556-56-9

allyl iodid

5-Hydroxy-1-methoxy-5-<3-(tetrahydropyran-2-yloxy)butynyl>benzocyclobuten-6-one
107245-43-2

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
107245-51-2

1-Methoxy-5-(2-propenyloxy)-5-<3-(tetrahydropyran-2-yloxy)butyn-1-yl>benzocyclobuten-6-one

Conditions
ConditionsYield
With silver carbonate In 1,4-dioxane99%
allyl iodid
556-56-9

allyl iodid

salicylaldehyde
90-02-8

salicylaldehyde

2-(1-hydroxy-3-butenyl)phenol
67472-23-5

2-(1-hydroxy-3-butenyl)phenol

Conditions
ConditionsYield
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
556-56-9

allyl iodid

methyl 6-deoxy-6-(p-tolylthio)-2,3,4-tri-O-benzyl-α-D-glucopyranoside
126360-02-9

methyl 6-deoxy-6-(p-tolylthio)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

Allyl-p-tolyl-((2S,3S,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethyl)-sulfonium; perchlorate

Allyl-p-tolyl-((2S,3S,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethyl)-sulfonium; perchlorate

Conditions
ConditionsYield
With silver perchlorate In acetonitrile for 48h; Ambient temperature;99%
allyl iodid
556-56-9

allyl iodid

3-Fluorobenzaldehyde
456-48-4

3-Fluorobenzaldehyde

(+/-)-1-(3'-fluorophenyl)but-3-en-1-ol
215320-36-8

(+/-)-1-(3'-fluorophenyl)but-3-en-1-ol

Conditions
ConditionsYield
With indium In water for 48h;99%

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