Zibo 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:43001-25-8
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquiryProduct Name: 4-Iodobut-1-yne Synonyms: 4-Iodobut-1-yne;4-Iodo-1-butyne;1-Iodobut-3-yne;3-Butynyl iodide;1-Butyne, 4-iodo- (9CI) CAS: 43001-25-8 MF: C4H5I MW: 179.99 EINECS: Product Categories: Mol File:
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Cas:43001-25-8
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
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
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
hight degree of purity Application:Fine chemical intermediates, used as the main raw material for he synthesis of various pesticides, medicines, surfactants, polymer monomers, Ond Ontifungal agents
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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
Cas:43001-25-8
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiryKnown for its best quality and competitve price, this chemicals we offered is widely appreciated by our customers.1) Standard:BP/USP/EP/Enterprise standard2) All Purity≥99%3) We are manufacturer and can provide high quality products with factory pric
Cas:43001-25-8
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryComprehensive range product, High quality, Quick shippment, COA with spectras Package:0.25g Application:pharmaceutical industry, food industry, research
Debyesci is here who supplied several kinds of chemical products to global pharmaceutical, drug discovery, agrochemical and biotechnology industries for four yearsOur key scientific leadership team has gained experience in top research and developmen
Cas:43001-25-8
Min.Order:0
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Type:Lab/Research institutions
inquiryhigh purity Application:Drug intermediates Materials intermediates and active molecules
1-butyn-4-ol
4-iodobut-1-yne
Conditions | Yield |
---|---|
With 1H-imidazole; iodine; triphenylphosphine In dichloromethane at 0 - 25℃; Inert atmosphere; | 73% |
With 1H-imidazole; iodine; triphenylphosphine In dichloromethane at 20℃; for 3h; Inert atmosphere; | 72% |
With 1H-imidazole; iodine; triphenylphosphine In dichloromethane at 20℃; for 4h; Inert atmosphere; | 68% |
3-butyn-1-yl p-toluenesulfonate
4-iodobut-1-yne
Conditions | Yield |
---|---|
With sodium iodide In acetone for 12h; | 50% |
With acetone; sodium iodide | |
With sodium iodide In acetone Heating; Yield given; |
methanesulfonic acid but-3-ynyl ester
4-iodobut-1-yne
Conditions | Yield |
---|---|
With sodium iodide In acetone for 22h; Reflux; | 4.1 g |
With sodium iodide In acetone for 4h; Inert atmosphere; Reflux; | |
With sodium iodide In acetone for 4h; Reflux; Inert atmosphere; |
4-bromobut-1-yne
4-iodobut-1-yne
Conditions | Yield |
---|---|
With sodium iodide In acetonitrile for 1h; Reflux; | |
With sodium iodide In dimethyl sulfoxide at 0 - 20℃; for 2h; |
4-iodobut-1-yne
3-(methylthio)-6-phenyl-1,2,4-triazine-5-thione
5-(3-butynylthio)-3-(methylthio)-6-phenyl-1,2,4-triazine
Conditions | Yield |
---|---|
With base | 100% |
With triethylamine In tetrahydrofuran for 6h; | 89% |
4-iodobut-1-yne
diethyl 2-(1,4-dioxaspiro[4.5]dec-6-en-8-ylmethyl)malonate
Conditions | Yield |
---|---|
Stage #1: diethyl 2-(1,4-dioxaspiro[4.5]dec-6-en-8-ylmethyl)malonate With sodium hydride In N,N-dimethyl-formamide at 0 - 20℃; Inert atmosphere; Stage #2: 4-iodobut-1-yne In N,N-dimethyl-formamide at 0 - 50℃; Inert atmosphere; | 99% |
5-phenyl-2H-[1,2,4]triazine-3-thione
4-iodobut-1-yne
3-(3-butylnylthio)-5-phenyl-1,2,4-triazine
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 24h; Ambient temperature; | 97% |
4-iodobut-1-yne
6-methyl-3-p-tolyl-1,2,4-triazine-5-thione
5-(3-butynylthio)-6-methyl-3-p-tolyl-1,2,4-triazine
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 6h; | 96% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 60℃; for 18h; Schlenk technique; | 96% |
With potassium carbonate In acetone at 65℃; for 7h; Schlenk technique; Sealed tube; | 94% |
With potassium carbonate In acetone at 60℃; for 18h; Inert atmosphere; |
4-iodobut-1-yne
thiosemicarbazide
S-3-butynylisothiosemicarbazide hydrogen iodide
Conditions | Yield |
---|---|
In ethanol at 78℃; for 6h; | 91% |
4-iodobut-1-yne
Conditions | Yield |
---|---|
With sodium sulfite In methanol; water for 48h; Reflux; | 91% |
4-iodobut-1-yne
5-methyl-1,2,4-triazine-6-thione
6-(3-butynylthio)-5-methyl-1,2,4-triazine
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 24h; Ambient temperature; | 90% |
Conditions | Yield |
---|---|
In acetonitrile for 15h; Reflux; | 90% |
Conditions | Yield |
---|---|
With sodium hydroxide In methanol for 24h; Ambient temperature; | 88% |
4-iodobut-1-yne
5-phenyl-1,2,4-triazine-6-thione
6-(3-butynylthio)-5-phenyl-1,2,4-triazine
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 24h; Ambient temperature; | 85% |
4-iodobut-1-yne
2-mercapto-5-phenylpyrimidine
2-(3-Butynylthio)-5-phenylpyrimidine
Conditions | Yield |
---|---|
With triethylamine In water at 70℃; for 1h; | 84% |
4-iodobut-1-yne
6-phenyl-3-p-tolyl-1,2,4-triazine-5-thione
5-(3-butynylthio)-6-phenyl-3-p-tolyl-1,2,4-triazine
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 6h; | 83% |
4-iodobut-1-yne
cis-1-Cyano-3-oxobicyclo<3.3.0>oct-1-ene
(3aS,3bS,6aR,7aR)-3-[1-Iodo-meth-(E)-ylidene]-7-oxo-decahydro-cyclopenta[a]pentalene-3a-carbonitrile
Conditions | Yield |
---|---|
With bis(tri-n-butyltin) In benzene at 80 - 85℃; for 0.666667h; Irradiation; | 81% |
Conditions | Yield |
---|---|
Stage #1: Isobutyronitrile With lithium diisopropyl amide In tetrahydrofuran at -78℃; Inert atmosphere; Stage #2: 4-iodobut-1-yne In tetrahydrofuran at -78 - 20℃; Inert atmosphere; | 79% |
formaldehyd
4-iodobut-1-yne
trimethylaluminum
(E)-5-iodo-3-methylpent-2-en-1-ol
Conditions | Yield |
---|---|
Stage #1: trimethylaluminum With zirconocene dichloride In dichloromethane; toluene at -20℃; for 0.5h; Negishi Coupling; Inert atmosphere; Stage #2: 4-iodobut-1-yne In dichloromethane; toluene; pentane at 20℃; for 2.5h; Negishi Coupling; Inert atmosphere; Stage #3: formaldehyd In dichloromethane; toluene; pentane at -30℃; for 0.25h; Inert atmosphere; | 76% |
Stage #1: trimethylaluminum With zirconocene dichloride In hexane; dichloromethane at 0℃; for 0.5h; Inert atmosphere; Stage #2: formaldehyd; 4-iodobut-1-yne In hexane; dichloromethane at 20℃; for 12h; Inert atmosphere; | 60% |
Conditions | Yield |
---|---|
With potassium hydroxide In tetrahydrofuran for 16h; Ambient temperature; | 74% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 48h; Ambient temperature; | 74% |
Conditions | Yield |
---|---|
With potassium carbonate at 60℃; for 4h; | 72% |
Conditions | Yield |
---|---|
With potassium carbonate at 80℃; for 6h; | 72% |
4-iodobut-1-yne
5-isopropyl-1,2,4-triazine-6-thione
6-(3-butynylthio)-5-isopropyl-1,2,4-triazine
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 24h; Ambient temperature; | 70% |
4-iodobut-1-yne
malonic acid dimethyl ester
dimethyl 2-(but-3-ynyl)malonate
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran for 48h; Heating; | 70% |
With sodium hydride 1.) DMF, 20 min; 2.) DMF, overnight; | 63% |
4-iodobut-1-yne
PVS
Conditions | Yield |
---|---|
With bis(tri-n-butyltin) In benzene at 80℃; Irradiation; Yield given; | A n/a B 68% |
With bis(tri-n-butyltin) In benzene at 80℃; Irradiation; Yields of byproduct given; | A n/a B 68% |
4-iodobut-1-yne
6-methyl-3-(methylthio)-1,2,4-triazine-5-thione
5-(3-butynylthio)-6-methyl-3-(methylthio)-1,2,4-triazine
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 6h; | 68% |
4-iodobut-1-yne
N-(2-bromoallyl)benzylamine
Conditions | Yield |
---|---|
In water at 70℃; for 48h; | 68% |
4-iodobut-1-yne
2-mercapto-4,6-dimethyl-pyrimidine hydrochloride
2-(3-Butynylthio)-4,6-dimethylpyrimidine
Conditions | Yield |
---|---|
With sodium hydroxide; triethylamine In water at 70℃; for 2h; | 66% |
4-iodobut-1-yne
acrylic acid methyl ester
A
methyl 3-iodo-2-cyclohexanecarboxylate
B
2-[1-Iodo-meth-(E)-ylidene]-cyclopentanecarboxylic acid methyl ester
Conditions | Yield |
---|---|
With bis(tri-n-butyltin) In benzene at 80℃; Irradiation; Yield given; | A n/a B 65% |
With bis(tri-n-butyltin) In benzene at 80℃; Irradiation; Yields of byproduct given; | A n/a B 65% |
4-iodobut-1-yne
2-mercapto-4-methylpyrimidine hydrochloride
2-(3-butynylthio)-4-methylpyrimidine
Conditions | Yield |
---|---|
With sodium hydroxide; triethylamine In water at 70℃; for 2h; | 64% |
4-iodobut-1-yne
6-carbethoxy-3-(methylthio)-1,2,4-triazine-5-thione
5-(3-butynylthio)-6-carbethoxy-3-(methylthio)-1,2,4-triazine
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 6h; | 64% |
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