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:3710-30-3
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
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
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
High quality and best price of 1,7-Octadiene from Henan Tianfu Chemical: Henan Tianfu Chemical Co.,LTD was built in 2009 with an ISO certificate in the past 5 years, we have grown up as a famous fine chemicals supplier in china and we had establi
A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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 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
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:3710-30-3
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
1,7-Octadiene Basic information Product Name: 1,7-Octadiene
Cas:3710-30-3
Min.Order:100 Gram
Negotiable
Type:Trading Company
inquiryHangzhou KieRaychem Co.,Ltd.is located in Yuhang District of Hangzhou City and specialized in the chemical product customization, development, sales, import and export. Current business is focused on fine chemicals, pharmaceutical materials and int
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
Best quality & Attractive price & Professional service; Trial & Pilot & CommercialHenan Fine Chemicals Co., LTD. is a diversified technology - oriented integrated company, which mainly concentrates on fine chemicals. Our company is committed to becom
Cas:3710-30-3
Min.Order:0
Negotiable
Type:Trading Company
inquiryAdequate stocks available,prompt shipment,Strictly control on quality,Timely after-sales
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
1,7-Octadiene can serve as a crosslinker and source of ethylene for a variant of Mori's conditions in CEYM-related reactions. Package:100 g in glass bottle Application:1,7-Octadiene has been used in a study to assess the structure and reaction rate i
2-(5-hexenyl)thiirane
1,7-Octadiene
Conditions | Yield |
---|---|
With hydrogen sulfide; triphenylphosphine; methyltrioxorhenium(VII) In [D3]acetonitrile for 1h; Ambient temperature; | 100% |
With tri-n-butyl-tin hydride; 2,2'-azobis(isobutyronitrile) In benzene Heating; | 85% |
Conditions | Yield |
---|---|
With triethanolamine; (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis-(2-phenylpyridine(-1H))-iridium(III) hexafluorophosphate; [Ni(2,2′:6′,2''-terpyridine)(pyridine)(CH3CN)2](PF6)2 In acetonitrile at 23 - 28℃; for 12h; Inert atmosphere; Sealed tube; Irradiation; | 98% |
With diethyl ether; sodium |
Conditions | Yield |
---|---|
With formic acid; triethylamine; tris(dibenzylideneacetone)dipalladium(0) chloroform complex; tributylphosphine In tetrahydrofuran for 4h; Heating; | 76% |
(E)-1-acetoxy-2,7-octadiene
1,7-Octadiene
Conditions | Yield |
---|---|
With formic acid; triethylamine; tris(dibenzylideneacetone)dipalladium(0) chloroform complex; tributylphosphine In tetrahydrofuran for 2h; Heating; | 67% |
With ammonium formate; tris(dibenzylideneacetone)dipalladium chloroform complex; tributylphosphine In 1,4-dioxane for 2h; Heating; | 100 % Chromat. |
7,8-diazabicyclo<4.2.2>dec-7-ene
A
(Z)-Cyclooctene
B
cis-bicyclo<4.2.0>octane
C
1,7-Octadiene
Conditions | Yield |
---|---|
With 4-tert-Butylcatechol In Petroleum ether at 160 - 170℃; for 69h; | A 14% B 23% C 30% |
In Petroleum ether at 160 - 170℃; for 69h; Mechanism; 4-t-butylpyrocatechol; | A 14% B 23% C 30% |
In Petroleum ether at 170℃; | |
In Petroleum ether at 170℃; also with deuterio labelled substrate; |
Conditions | Yield |
---|---|
With lanthanum; iodine In tetrahydrofuran at 67℃; for 2h; | 26% |
With α-picoline; manganese; trifluoroacetic acid; cobalt(II) bromide In acetonitrile at 50℃; | |
With triethanolamine; (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis-(2-phenylpyridine(-1H))-iridium(III) hexafluorophosphate; [Ni(2,2′:6′,2''-terpyridine)(pyridine)(CH3CN)2](PF6)2 for 12h; Irradiation; Inert atmosphere; |
Conditions | Yield |
---|---|
In tetrahydrofuran-d8 at 22℃; Inert atmosphere; Schlenk technique; | A 22% B 22% |
Conditions | Yield |
---|---|
In hexane at 16 - 18℃; under 53203.6 Torr; Pressure; Temperature; | 20.1% |
at 25 - 80℃; under 30003 - 150015 Torr; for 24 - 42h; Product distribution / selectivity; |
Conditions | Yield |
---|---|
palladium anchored polystyrene In neat (no solvent) at 25℃; under 1551.4 Torr; for 36h; | A 20% B 20% |
palladium anchored polystyrene In neat (no solvent) at 25℃; under 1551.4 Torr; for 36h; | A 20% B 20% |
Conditions | Yield |
---|---|
Stage #1: buta-1,3-diene With TEMPOL; sodium methylate; palladium diacetate In 1-methyl-pyrrolidin-2-one at -5 - 75℃; under 7500.75 Torr; Inert atmosphere; Stage #2: With formic acid In 1-methyl-pyrrolidin-2-one at 80 - 90℃; under 15001.5 Torr; Product distribution / selectivity; Inert atmosphere; | A 5.5% B 94.3 %Chromat. |
With formic acid; triethylamine; palladium diacetate; triphenylphosphine In DMF (N,N-dimethyl-formamide) at 90℃; under 750.075 Torr; for 1.5h; Product distribution / selectivity; |
Conditions | Yield |
---|---|
With ammonium sulfate; ammonia; sodium Reagens 4: Aether; | |
With ethylene dibromide; copper(I) bromide; lithium bromide; zinc In tetrahydrofuran; ethanol Heating; |
Conditions | Yield |
---|---|
at 500℃; Pyrolysis; |
Conditions | Yield |
---|---|
With diethyl ether |
Conditions | Yield |
---|---|
With diethyl ether |
(Z)-Cyclooctene
1,7-Octadiene
Conditions | Yield |
---|---|
at 550℃; | |
at 633℃; Thermodynamic data; Rate constant; further temp.; energy of activation; |
Conditions | Yield |
---|---|
at 500℃; |
Conditions | Yield |
---|---|
With acetic anhydride; bis-triphenylphosphine-palladium(II) chloride at 250℃; under 735.5 Torr; Yield given; | |
Stage #1: 1,10-decanedioic acid With bis(1,5-cyclooctadiene)diiridium(I) dichloride; triphenylphosphine; potassium iodide at 20℃; for 0.5h; Inert atmosphere; Schlenk technique; Stage #2: With acetic anhydride at 160℃; for 5h; Inert atmosphere; Schlenk technique; regioselective reaction; | |
With formate dehydrogenase; 1200 U catalase; OleT in combination with the putidaredoxin electron-transfer system CamAB; P450 monooxygenase OleT; ammonium formate; β-nicotinamide adenine dinucleotide, disodium salt, reduced form In ethanol at 4℃; for 72h; Catalytic behavior; Enzymatic reaction; | |
Multi-step reaction with 2 steps 1: P450 monooxygenase OleT; OleT in combination with the putidaredoxin electron-transfer system CamAB; formate dehydrogenase; β-nicotinamide adenine dinucleotide, disodium salt, reduced form; 1200 U catalase; ammonium formate / ethanol / Enzymatic reaction 2: P450 monooxygenase OleT; OleT in combination with the putidaredoxin electron-transfer system CamAB; formate dehydrogenase; β-nicotinamide adenine dinucleotide, disodium salt, reduced form; 1200 U catalase; ammonium formate / ethanol / Enzymatic reaction View Scheme |
bicyclo<4.2.0>octane
A
ethene
B
1,7-Octadiene
C
cyclohexene
Conditions | Yield |
---|---|
In pentane Quantum yield; Irradiation; |
Conditions | Yield |
---|---|
With ammonium formate; tris(dibenzylideneacetone)dipalladium chloroform complex; tributylphosphine In 1,4-dioxane for 2h; Heating; | A 2 % Chromat. B 98 % Chromat. |
Conditions | Yield |
---|---|
With ammonium formate; tris(dibenzylideneacetone)dipalladium chloroform complex; tributylphosphine In 1,4-dioxane for 2h; Heating; | A 1 % Chromat. B 99 % Chromat. |
Conditions | Yield |
---|---|
at 633℃; Rate constant; further temperature; |
Conditions | Yield |
---|---|
at 300.1℃; Rate constant; Thermodynamic data; further temperatures; energy of activation; ΔH(exit.); ΔS(exit.); |
(E)-cyclooctene
A
(Z)-Cyclooctene
B
vinylcyclohexane
C
1,7-Octadiene
Conditions | Yield |
---|---|
at 512℃; Rate constant; further temperatures; |
Conditions | Yield |
---|---|
With ammonium formate; tris(dibenzylideneacetone)dipalladium chloroform complex; tributylphosphine In 1,4-dioxane for 2h; Heating; | A 4 % Chromat. B 96 % Chromat. |
Conditions | Yield |
---|---|
With ammonium formate; tris(dibenzylideneacetone)dipalladium chloroform complex; tributylphosphine In 1,4-dioxane for 2h; Heating; | A 30 % Chromat. B 70 % Chromat. |
With ammonium formate; bis-triphenylphosphine-palladium(II) chloride; triphenylphosphine In 1,4-dioxane at 100℃; for 2h; Product distribution; other catalysts, other ligands; | A 21 % Chromat. B 79 % Chromat. |
With ammonium formate; tris(dibenzylideneacetone)dipalladium(0) chloroform complex; triethyl phosphite In 1,4-dioxane for 2h; Product distribution; Heating; var. catalyst,; | A 26 % Chromat. B 74 % Chromat. |
Conditions | Yield |
---|---|
With ammonium formate; tris(dibenzylideneacetone)dipalladium chloroform complex; tributylphosphine In 1,4-dioxane for 2h; Heating; | A 1 % Chromat. B 99 % Chromat. |
7,8-diazabicyclo<4.2.2>dec-7-ene
A
(Z)-Cyclooctene
B
cis-bicyclo<4.2.0>octane
C
1,7-Octadiene
Conditions | Yield |
---|---|
In cyclohexane at 170℃; Product distribution; Mechanism; var. temps; also direct and sensitised photolysis; | A 18 % Chromat. B 35 % Chromat. C 47 % Chromat. |
(E)-8-chloro-octa-1,6-diene
1,7-Octadiene
Conditions | Yield |
---|---|
With sodium formate; tris(dibenzylideneacetone)dipalladium chloroform complex; tributylphosphine In 1,4-dioxane for 2h; Heating; | 100 % Chromat. |
cis-8-thiabicyclo<4.3.0>nonane 8,8-dioxide
A
buta-1,3-diene
B
1,7-Octadiene
C
benzene
Conditions | Yield |
---|---|
at 850℃; under 0.005 Torr; Product distribution; other temperature (925 deg C); flash vacuum pyrolysis of bi- and tricyclic sulfones; | A n/a B 41 % Spectr. C 2 % Spectr. |
Conditions | Yield |
---|---|
at 336.9 - 817.9℃; Kinetics; Thermodynamic data; activation energy; |
Conditions | Yield |
---|---|
With hydrogen; sodium triethylborohydride In tetrahydrofuran at 23℃; under 30402 Torr; for 24h; Catalytic behavior; Inert atmosphere; Schlenk technique; | 100% |
With [Re(NO)(η(2)-H2)Br2(PiPr3)2]; dimethylamine borane; hydrogen at 90℃; under 7500.75 Torr; for 0.2h; Autoclave; | 88% |
With hydrogen; sodium triethylborohydride In tetrahydrofuran at 23℃; under 30003 Torr; for 48h; Reagent/catalyst; Autoclave; | 82% |
Conditions | Yield |
---|---|
With diazomethyl-trimethyl-silane; ruthenium Schiff-base In toluene at 70℃; for 1h; ring-closing metathesis; | 100% |
With diazomethyl-trimethyl-silane; ruthenium In toluene at 85℃; for 17h; Product distribution; Further Variations:; Catalysts; | 100% |
[2-((2,6-iPr2-Ph-imino)methyl)phenol][p-cymene][=CHPh]Ru2Cl3 In various solvent(s) at 70℃; for 4h; Product distribution; Further Variations:; Catalysts; Temperatures; | 100% |
Conditions | Yield |
---|---|
With palladium diacetate; triethylamine; triphenylphosphine In N,N-dimethyl-formamide at 150℃; for 24h; Heck Reaction; | 100% |
With palladium diacetate; triethylamine; triphenylphosphine In N,N-dimethyl-formamide at 150℃; for 24h; Heck Reaction; | 100% |
Conditions | Yield |
---|---|
With [2-(i-PrO)-C6H4]C(H)=RuCH[(Mes)NCH2CH2N(Mes)]Cl2 In toluene at 90℃; for 20h; Diels-Alder reaction; Sealed tube; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With [2-(i-PrO)-C6H4]C(H)=RuCH[(Mes)NCH2CH2N(Mes)]Cl2 In toluene at 90℃; for 20h; Diels-Alder reaction; Sealed tube; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With [2-(i-PrO)-C6H4]C(H)=RuCH[(Mes)NCH2CH2N(Mes)]Cl2 In toluene at 90℃; for 20h; Diels-Alder reaction; Sealed tube; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With [2-(i-PrO)-C6H4]C(H)=RuCH[(Mes)NCH2CH2N(Mes)]Cl2 In toluene at 90℃; for 20h; Diels-Alder reaction; Sealed tube; Inert atmosphere; | 99% |
1,7-Octadiene
phenylacetylene
[1,4]naphthoquinone
2-phenyl-1,4,4a,9a-tetrahydroanthracene-9,10-dione
Conditions | Yield |
---|---|
With [2-(i-PrO)-C6H4]C(H)=RuCH[(Mes)NCH2CH2N(Mes)]Cl2 In toluene at 90℃; for 20h; Diels-Alder reaction; Sealed tube; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With [2-(i-PrO)-C6H4]C(H)=RuCH[(Mes)NCH2CH2N(Mes)]Cl2 In toluene at 90℃; for 20h; Diels-Alder reaction; Sealed tube; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With cobalt pivalate; 1-adamantyl isocyanide at 80℃; for 24h; Inert atmosphere; | 99% |
With cobalt pivalate; [1,3-bis(2,4,6-trimethylphenyl)imidazol]-2-ylidene at 80℃; for 24h; Inert atmosphere; | 60% |
2,4-bis[2,6-bis(2,4,6-trimethylphenyl)phenyl]-1,3-diphospha-2,4-diazacyclobutane
1,7-Octadiene
Conditions | Yield |
---|---|
In benzene at 20℃; for 1h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With diethylzinc In hexane; acetonitrile at -20℃; for 16h; Schlenk technique; Inert atmosphere; | 99% |
tetrafluoroboric acid diethyl ether
1,7-Octadiene
Conditions | Yield |
---|---|
In chlorobenzene under N2, addn. of HBF4*OEt2 to cooled soln. of Re-compd. at -45°C, then addn. of diene to the intermediate with stirring, stirring 15 h at 100°C; soln. filtered into hexane, filtration, washing (pentane), drying, mixt. of isomers; | 98% |
Conditions | Yield |
---|---|
With [2-(i-PrO)-C6H4]C(H)=RuCH[(Mes)NCH2CH2N(Mes)]Cl2 In toluene at 90℃; Sealed tube; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
With [2-(i-PrO)-C6H4]C(H)=RuCH[(Mes)NCH2CH2N(Mes)]Cl2 In toluene at 90℃; for 20h; Diels-Alder reaction; Sealed tube; Inert atmosphere; | 98% |
1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
1,7-Octadiene
1,1,1,2,2,3,3,4,4,13,13,14,14,15,15,16,16,16-octadecafluoro-6,11-diiodohexadecane
Conditions | Yield |
---|---|
With Sodium thiosulfate pentahydrate; 2,2'-azobis-(2,4-dimethylvaleronitrile) at 85℃; for 3h; | 97.5% |
(E)-1-phenyl-N-(1-phenylethylidene)methanamine
1,7-Octadiene
Conditions | Yield |
---|---|
Stage #1: (E)-1-phenyl-N-(1-phenylethylidene)methanamine; 1,7-Octadiene With molecular sieve; tris(triphenylphosphine)rhodium(I) chloride In toluene at 150℃; for 2h; Stage #2: With water Acid hydrolysis; Stage #3: With hydrogen; palladium on activated charcoal | 97% |
triphenylmethylacetonitrile oxide
1,7-Octadiene
5-(5-hexenyl)-3-(triphenylmethyl)-2-isoxazoline
Conditions | Yield |
---|---|
In benzene for 48h; Heating; | 96% |
Conditions | Yield |
---|---|
With 3-chloro-benzenecarboperoxoic acid In dichloromethane at 0℃; | 95% |
With 3-chloro-benzenecarboperoxoic acid at 10 - 23℃; for 16h; | 95.2% |
With 3-chloro-benzenecarboperoxoic acid In dichloromethane at 0 - 20℃; for 24h; | 94% |
Conditions | Yield |
---|---|
With manganese dioxide; dihydrogen peroxide In 1,4-dioxane; acetic acid | 95% |
With manganese dioxide; dihydrogen peroxide In 1,4-dioxane | 51% |
1,7-Octadiene
3,5-bis(trifluoromethyl)phenylacetylene
diethyl Fumarate
Conditions | Yield |
---|---|
With [2-(i-PrO)-C6H4]C(H)=RuCH[(Mes)NCH2CH2N(Mes)]Cl2 In toluene at 90℃; for 30h; Diels-Alder reaction; Sealed tube; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
With C29H31F3I2N2RuS In benzene-d6 at 80℃; for 1h; | 95% |
Conditions | Yield |
---|---|
[Y(C5Me4CH2SiMe2NCMe3)(THF)] In hexane at 20℃; for 48h; | 94% |
With ((HBPIMes,H)FeBr2); sodium triethylborohydride at 20℃; for 24h; Inert atmosphere; Schlenk technique; | 14% |
1,7-Octadiene
(E,E)-2,6-octadiene
Conditions | Yield |
---|---|
With C24H42N2PRu(1+)*F6P(1-) In [(2)H6]acetone at 20℃; for 0.166667h; stereoselective reaction; | 94% |
Conditions | Yield |
---|---|
With hydrogenchloride; oxygen; copper dichloride; palladium dichloride In tetrahydrofuran under 760 Torr; for 18h; Ambient temperature; | 93% |
Conditions | Yield |
---|---|
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex at 70 - 90℃; for 24h; | 93% |
With dihydrogen hexachloroplatinate; platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex In toluene at 70 - 90℃; for 24.1667h; | 93% |
perfluoroisopropyl iodide
1,7-Octadiene
9,10,10,10-Tetrafluoro-7-iodo-9-trifluoromethyldec-1-ene
Conditions | Yield |
---|---|
With bis(cyclopentadienyl)titanium dichloride; iron In ethanol at 55℃; for 10h; other per(poly)fluoroalkyl iodides and bromides; | 92% |
With bis(cyclopentadienyl)titanium dichloride; iron In ethanol at 55℃; for 10h; | 92% |
Conditions | Yield |
---|---|
With cobalt(II) bromide-[1,2-bis(diphenylphosphino)ethane]; zinc(II) iodide; zinc In dichloromethane for 20h; | 92% |
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