CAS No.768-56-9,4-Phenyl-1-butene Suppliers,MSDS download

Dayang Chem (Hangzhou) Co.,Ltd.

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

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Simagchem Corporation

Welcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our

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Ality Chemical Corporation

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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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

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Henan Tianfu Chemical Co., Ltd.

Our company was built in 2009 with an ISO certificate.In the past 6 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.O

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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

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Zibo Hangyu Biotechnology Development Co., Ltd

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

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Hangzhou Huarong Pharm Co., Ltd.

Hangzhou Huarong Pharm Co., Ltd.established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World. Hu

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Hunan chemfish Pharmaceutical co.,Ltd

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GIHI CHEMICALS CO.,LIMITED

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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

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Aecochem Corp.

Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS

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Zhuozhou Wenxi import and Export Co., Ltd

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

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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

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Changchun Artel lmport and Export trade company

Supply top quality products with a reasonable price Application:api

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Hunan Russell Chemicals Technology Co.,Ltd

high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China

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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

but-3-enylbenzene

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HENAN SUNLAKE ENTERPRISE CORPORATION

HENAN SUNLAKE ENTERPRISE CORPORATION Our company advantages: 1、The highest quality with the competitive price. 2、Professional human services. 3、The fastest and safest delivery service. 4、The faster and safest delivery service. 5、The hig

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SuZhou LaiTeou

1, Quality: Our company is a professional production of intermediates and chemicals for many years, our products have exported to Germany, Spain, UK, USA, Australia, Middle East, and so on other country, and we have got very good feedback fro

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Watson International Ltd

Watson International Ltd' has a very strong R&D and technical capacity supported by FCAD's platform. The subsidiaries under FCAD Group have accumulated much know-how of different fine chemical branches. For example, Apnoke Scientific L

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Hebei Ruishun Trade Co.,Ltd

Profile HeBei Ruishun Trade Co.LTD, registered capital one million,have a production of pharmaceutical raw materials, pharmaceutical raw materials factory reagent r&d center,Seek development by credit

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Xiamen BaiFuchem Co.,Ltd

BaiFuChem is a Professional chemical raw material supplier in China, our main products include Biochemical , Pharma Intermediate and Organic chemical etc. BaiFuChem have wealth of products,experience , expertise and state-of-the-art

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AOPHARM

Aopharm is specialized in APIs, pharmaceutical intermediates & fine chemicals. 1. The best quality, competitive price. 2. The best service before or after shipment. 3. Rich experience in export operation. 4. Rich experience in modes of

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ORCHID CHEMICAL SUPPLIES LTD

4-Phenyl-1-Butylene supplierAppearance:pale red crystal powder Storage:Keep away of light，cool place Package:25kg/drum;200kg/drum Application:Pharma Intermediate Transportation:Sea/air/courier

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Shanghai united Scientific Co.,Ltd.

United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat

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Chungking Joyinchem Co., Ltd.

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Hangzhou Yierdechem Co. Ltd

With about ten years experiences in the field of pharmaceutical chemicals, Yierdechem has established solid business cooperation relationships with many large companys worldwide.As a leading supplier of API and pharmaceutical intermediates, holds its

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Henan Wising Chem Co., Ltd

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Pure Chemistry Scientific Inc.

4-Phenyl-1-butene Application:816158

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Nanjing Raymon Biotech Co., Ltd.

Benzene, 3-buten-1-yl- Storage:keep in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/pharma intermediate Transportation:By Sea,by Air,By courier like DHL or Fedx. Port:Shanghai/Shenzhen

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Synthetic route

: 1589-82-8
phenylmagnesium bromide

: 106-95-6
allyl bromide

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran; diethyl ether at 20℃; for 0.25h;	100%

: 16520-62-0
4-Phenyl-1-butyne

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With sodium dodecylbenzenesulfonate; hydrogen; palladium diacetate In water at 25℃; under 760.051 Torr; for 1h;	99%
With sodium hydroxide; sodium tetrahydroborate; tetrakis(triphenylphosphine) palladium(0) In methanol; water at 20℃; for 0.666667h;	95%
With hydrogen In ethanol at 20℃; under 760.051 Torr; for 3h;	95%

: 100-39-0
benzyl bromide

: 1730-25-2
allylmagnesium bromide

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
In tetrahydrofuran at 20℃; for 4h;	97%
In tetrahydrofuran; diethyl ether at 0 - 20℃; for 8h; Schlenk technique;	50%
With dodecane; C20H14Cl5FeN2O2 In diethyl ether at 20℃; for 0.5h; Catalytic behavior; Schlenk technique;	13%

: 16520-62-0
4-Phenyl-1-butyne

A: 768-56-9
4-Phenyl-1-butene

B: 104-51-8
1-butylbenzene

Conditions

Conditions	Yield
With hydrogen In hexane at 40℃; under 760.051 Torr; for 3h;	A 97% B 3%
With lithium; isopropyl alcohol; nickel dichloride; 4,4'-di-tert-butylbiphenyl In tetrahydrofuran at 20℃; for 24h;	A 87 % Turnov. B n/a

: 1634-04-4
tert-butyl methyl ether

: 100-44-7
benzyl chloride

: 107-05-1
3-chloroprop-1-ene

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With sulfuric acid; nitrogen In tetrahydrofuran; water; iodine	93%

...Expand

: 100-44-7
benzyl chloride

: 107-05-1
3-chloroprop-1-ene

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With sulfuric acid; nitrogen In tetrahydrofuran; water; iodine; toluene	92%

: 100-39-0
benzyl bromide

: 106-95-6
allyl bromide

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With palladium diacetate; copper(II) acetate monohydrate; ammonium bromide; lithium chloride In water; N,N-dimethyl-formamide at 0℃; for 12h; Electrochemical reaction;	91%
With indium In tetrahydrofuran at 20℃; for 1.5h;	75%
With diethyl ether; sodium

: 16212-05-8
(allylsulfonyl)benzene

: 1589-82-8
phenylmagnesium bromide

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With triphenylphosphine; copper dichloride In tetrahydrofuran at 60℃;	90%

: 71813-50-8
1-bromo-2-(but-3-enyl)benzene

A: 767-58-8
1-methylindane

B: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With 2-H-1,3-di-tert-butyl-1,3,2-diazaphosphorinane; 2,2'-azobis(isobutyronitrile) In toluene at 90℃; for 8h; chemoselective reaction;	A 90% B n/a
With tetrabutylammonium perchlorate In N,N-dimethyl-formamide direct-electrochemical reduction on Pt electrode; Epc = -2.80 V;	A 35% B 16%
With tetrabutylammonium perchlorate In N,N-dimethyl-formamide direct-electrochemical reduction on Pt Epc = -2.80 V;	A 35% B 16%

: 104-53-0
3-phenyl-propionaldehyde

: 31729-70-1
bis(iodozinc)methane

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
In tetrahydrofuran at 60℃; for 0.05h; Microflow system;	89%
With titanium chloride 1.) THF, 20 deg C, 2 h, 2.) THF, 0-20 deg C, 1 h; Yield given. Multistep reaction;

: 100-39-0
benzyl bromide

: 107-05-1
3-chloroprop-1-ene

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With palladium diacetate; copper(II) acetate monohydrate; ammonium bromide; lithium chloride In water; N,N-dimethyl-formamide at 0℃; for 12h; Electrochemical reaction;	88%
With potassium hydrogencarbonate In water; isopropyl alcohol at 20℃; for 12h; Electrochemical reaction;	95 %Chromat.

: cis-{(PhCH2)2Co(III)(2,2'-bipyridine)2}ClO4

: 106-95-6
allyl bromide

A: 747369-48-8
(Co(bpy)2Br)(1+)

B: 592-42-7
1,5-Hexadien

C: 768-56-9
4-Phenyl-1-butene

D: 103-29-7
1,1'-(1,2-ethanediyl)bisbenzene

Conditions

Conditions	Yield
In [D3]acetonitrile Kinetics; Irradiation (UV/VIS); Degasses condition, 298 K, 11 h;; detected by NMR-spectroscopy;;	A n/a B 36% C 34% D 85%

...Expand

: cis-{(PhCH2)2Co(bpy)2}(1+)

: 106-95-6
allyl bromide

A: 747369-48-8
(Co(bpy)2Br)(1+)

B: 592-42-7
1,5-Hexadien

C: 768-56-9
4-Phenyl-1-butene

D: 103-29-7
1,1'-(1,2-ethanediyl)bisbenzene

Conditions

Conditions	Yield
In [D3]acetonitrile Kinetics; Irradiation (UV/VIS); Degasses condition, 298 K, 11 h;; detected by NMR-spectroscopy;;	A n/a B 36% C 34% D 85%

...Expand

: 2622-05-1
allylmagnesium bromide

: 100-39-0
benzyl bromide

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
	83%

: 100-51-6
benzyl alcohol

: 762-72-1
allyl-trimethyl-silane

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With titanium tetrachloride In dichloromethane at 20℃; for 0.166667h;	83%
With indium(III) chloride; trimethylsilyl bromide In hexane for 4h; Heating;	68%

: 203458-12-2
C17H19NO4S2

: 6921-34-2
benzylmagnesium chloride

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With copper(l) iodide In tetrahydrofuran at 70℃; for 1h; Inert atmosphere; regioselective reaction;	83%

: 24850-33-7
allyltributylstanane

: 100-39-0
benzyl bromide

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With chloro(dimethylsulfide) gold(I) In neat (no solvent) at 50℃; for 3h; Inert atmosphere;	82%
Pd(NCOC2H4CO)(PPh3)2Br In toluene at 60℃; for 48h; Stille cross-coupling;	31%
With 0.1 wt% Au nanoparticles deposited on boron-doped carbon In neat (no solvent) at 50℃; for 72h; Stille Cross Coupling;

: 64283-87-0
4-phenyl-1-iodobutane

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With potassium carbonate In acetonitrile at 50℃; for 2h; Irradiation;	80%
With potassium carbonate In acetonitrile at 20℃; Irradiation;	99 % Chromat.

: 3047-25-4
1-(but-3-en-1-yl)-2-chlorobenzene

A: 767-58-8
1-methylindane

B: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With potassium In ammonium hydroxide; tert-butyl alcohol Heating;	A 80% B 17.9%
With potassium In ammonia; tert-butyl alcohol Product distribution; Mechanism; Heating; other o-(3-butenyl)halobenzene; var. alkali metals and conc.;	A 80% B 17.9%
With potassium In ammonium hydroxide; tert-butyl alcohol Heating;	A 72.5% B 24.8%

: 125763-09-9
3-benzyl-4-(bromomethyl)oxetan-2-one

A: 935-00-2
trans-4-phenyl-2-butene

B: 768-56-9
4-Phenyl-1-butene

C: 15324-90-0
(2Z)-but-2-en-1-ylbenzene

: rac-(3R,4R)-3-benzyl-4-methyloxetan-2-one

Conditions

Conditions	Yield
With diphenyl diselenide; tri-n-butyl-tin hydride In benzene for 4h; Ambient temperature; Title compound not separated from byproducts;	A n/a B n/a C n/a D 80%

...Expand

: 2270-20-4
5-Phenylpentanoic acid

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With 2,2-dimethylpropanoic anhydride; bis[2-(diphenylphosphino)phenyl] ether; palladium dichloride In various solvent(s) at 110℃; for 16h;	80%
With acridine; chloropyridinecobaloxime(III) In dichloromethane; acetonitrile at 25 - 27℃; for 36h; Irradiation;	66%
With bis(triphenylphosphine)iridium(I) carbonyl chloride; acetic anhydride; potassium iodide at 160℃; for 5h; Inert atmosphere;
With carbon monoxide; 1,5-bis-(diphenylphosphino)pentane; acetic anhydride; potassium iodide; iron(II) chloride at 240℃; under 15201 Torr; for 3h;	60 %Spectr.

: 1126-76-7
1,2-Epoxy-4-phenylbutane

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With bis(cyclopentadienyl)titanium dichloride; manganese In tetrahydrofuran at 20℃; Inert atmosphere;	80%

: 4360-60-5
2-phenethyl-[1,3]dioxolane

: 13170-43-9
(trimethylsilyl)methylmagnesium chloride

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
Stage #1: (trimethylsilyl)methylmagnesium chloride With zinc(II) iodide In diethyl ether for 6h; Addition; Heating; Stage #2: 2-phenethyl-[1,3]dioxolane In benzene for 8h; Grignard reaction; Heating; Further stages.;	79%

: 762-73-2
trimethyl(allyl)stannane

: 100-39-0
benzyl bromide

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
under 7500600 Torr;	78%

: 592-41-6
1-hexene

: 75456-62-1
(4-methoxybut-3-en-1-yl)benzene

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With lithium perchlorate In nitromethane Electrochemical reaction;	78%

: 100-59-4
phenylmagnesium chloride

: 7051-34-5
cyclopropylcarbinyl bromide

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With [((Me)NN2)NiCl] Kumada-Corriu-Tamao coupling reaction; Inert atmosphere;	78%
With [Fe(bis(oxazolinylphenyl)amido-Ph)Cl2] In tetrahydrofuran at 20℃; for 2h; Inert atmosphere;	48%

: 87837-53-4
(E)-[(4-phenylbut-1-en-1-yl)sulfonyl]benzene

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With disodium telluride	75%
Stage #1: (E)-[(4-phenylbut-1-en-1-yl)sulfonyl]benzene With n-butyllithium; zirconocene dichloride In tetrahydrofuran; hexane at 50℃; for 0.25h; Stage #2: With hydrogenchloride; water In tetrahydrofuran; hexane at -20 - 20℃; Further stages.;	67%

: 154233-17-7
(2-hydroxy-4-phenyl-butyl)-phosphonic acid diethyl ester

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
Stage #1: (2-hydroxy-4-phenyl-butyl)-phosphonic acid diethyl ester With sodium hydroxide In methanol at 20℃; for 16h; Stage #2: With dacarbazine In chloroform at 20℃; for 4h; Further stages.;	75%

: 75553-23-0, 106262-48-0, 39520-63-3
5-phenylpenta-2-en-1-ol

: 768-56-9
4-Phenyl-1-butene

Conditions

Conditions	Yield
With methoxy(cyclooctadiene)rhodium(I) dimer; N,N-Dimethylacrylamide; 3-Methoxybenzoic acid; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene In toluene at 90℃; for 24h; Inert atmosphere; Glovebox; Sealed tube;	75%

: 768-56-9
4-Phenyl-1-butene

: 1126-76-7
1,2-Epoxy-4-phenylbutane

Conditions

Conditions	Yield
With 3-chloro-benzenecarboperoxoic acid In chloroform	100%
With 3-chloro-benzenecarboperoxoic acid In dichloromethane at 0 - 25℃;	100%
With 3-chloro-benzenecarboperoxoic acid In dichloromethane at 20℃; Cooling with ice;	100%

: 768-56-9
4-Phenyl-1-butene

: 507-09-5
thioacetic acid

: 294201-60-8
S-(4-phenylbutyl) ethanethioate

Conditions

Conditions	Yield
In dichloromethane for 0.5h; Irradiation;	100%
With benzo[de]benzo[4,5]imidazo[2,1-a]isoquinolin-7-one In cyclohexane at 20℃; for 1h; Inert atmosphere; Sealed tube; Irradiation;	98%

: 768-56-9
4-Phenyl-1-butene

: 104-51-8
1-butylbenzene

Conditions

Conditions	Yield
With 4,4'-di-tert-butylbiphenyl; lithium; isopropyl alcohol; nickel dichloride In tetrahydrofuran at 20 - 76℃; Inert atmosphere; chemoselective reaction;	99%
With 2,6-bis[1-(2,6-diisopropylphenylimino)ethyl]pyridine cobalt(II) dichloride; diethoxymethylane; sodium triethylborohydride In toluene at -78 - 20℃; for 5h;	96%
With aluminum (III) chloride; manganese; cobalt(II) diacetate tetrahydrate; isopropyl alcohol at 22℃; Reagent/catalyst;	96%

: 768-56-9
4-Phenyl-1-butene

: 124888-60-4, 124988-64-3, 143615-31-0, 1199-97-9
4-phenylbutane-1,2-diol

Conditions

Conditions	Yield
With water; 4-methylmorpholine N-oxide In dichloromethane; tert-butyl alcohol at 20℃; for 48h; Inert atmosphere;	99%
With 4-methylmorpholine N-oxide In water; acetone at 20℃; for 3h; Inert atmosphere;	97%
With O4Os(2-)*C123H141N3O28(2+); 4-methylmorpholine N-oxide In water; acetonitrile at 20℃; for 1h; Inert atmosphere;	95%

: 355-43-1
n-perfluorohexyl iodide

: 768-56-9
4-Phenyl-1-butene

: (5,5,6,6,7,7,8,8,9,9,10,10,10-tridecafluoro-3-iododecyl)benzene

Conditions

Conditions	Yield
With pyrrolidine; Diphenylacetaldehyde In dichloromethane at 20℃; for 16h; Inert atmosphere; Irradiation;	99%
With sodium triethylborohydride In hexane for 6h; Ambient temperature;	82.8%

: 64-17-5
ethanol

: 768-56-9
4-Phenyl-1-butene

: 19158-51-1
P-toluenesulfonyl cyanide

A: 1858-86-2, 59153-38-7, 59203-02-0, 112458-71-6
Ethyl p-toluenesulfinate

B: 73475-33-9
2-methyl-4-phenylbutanenitrile

Conditions

Conditions	Yield
With phenylsilane; ethanediamino-N,N'-bis(salicylidene)-based cobalt catalyst at 23℃; for 1h;	A n/a B 99%

...Expand

: 768-56-9
4-Phenyl-1-butene

: 1159486-39-1
2-(4-tert-butyl-2,2,6,6-tetraethyl-3-oxo-piperazin-1-yloxy)-malonic acid dimethyl ester

: 1159486-41-5
2-[2-(4-tert-butyl-2,2,6,6-tetraethyl-3-oxo-piperazin-1-yloxy)-4-phenyl-butyl]-malonic acid dimethyl ester

Conditions

Conditions	Yield
In 1,2-dichloro-ethane at 125℃; for 2h;	99%

: 5542-49-4
piperidin-1-yl benzoate

: 768-56-9
4-Phenyl-1-butene

: 41208-52-0
1-(4-phenylbutyl)piperidine

Conditions

Conditions	Yield
With diethoxymethylane; copper diacetate; 5,5′-bis[di(3,5-di-tert-butyl-4-methoxyphenyl)phosphino]-4,4′-bi-1,3-benzodioxole In tetrahydrofuran at 40℃; for 36h; Glovebox; regioselective reaction;	99%

: 768-56-9
4-Phenyl-1-butene

: 694-53-1
phenylsilane

: 1351520-69-8
1-phenyl-4-(phenylsilyl)butane

Conditions

Conditions	Yield
With C66H106N4O6Sm2 In toluene at 60℃; for 5h; Inert atmosphere; Glovebox; Schlenk technique; regioselective reaction;	99%
With C10H14CoO5; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene In tetrahydrofuran at 20℃; for 3h; regioselective reaction;	93%
With nickel(II) chloride hexahydrate; potassium tert-butylate In tetrahydrofuran at -30℃; for 1h; Schlenk technique; Inert atmosphere; Sealed tube;	91%

: 768-56-9
4-Phenyl-1-butene

: 1512-30-7
difluoromethylsulfonyl chloride

: (3-chloro-5,5-difluoropentyl)benzene

Conditions

Conditions	Yield
With dilauryl peroxide In dichloromethane at 70℃; for 8h; Reagent/catalyst; Solvent; Temperature; Inert atmosphere;	99%

: 768-56-9
4-Phenyl-1-butene

: 75-66-1
2-methylpropan-2-thiol

: tert-butyl(4-phenylbutyl)sulfane

Conditions

Conditions	Yield
With benzo[de]benzo[4,5]imidazo[2,1-a]isoquinolin-7-one In cyclohexane at 20℃; for 1h; Inert atmosphere; Sealed tube; Irradiation;	99%
With methanesulfonic acid; 1,1-bis(tert-butylperoxy)cyclohexane In acetonitrile at 20℃;	88%
With methanesulfonic acid; 1,1-bis(tert-butylperoxy)cyclohexane In acetonitrile at 20℃; Schlenk technique;	88%

: 677-69-0
perfluoroisopropyl iodide

: 768-56-9
4-Phenyl-1-butene

: (E)-(5,6,6,6-tetrafluoro-5-(trifluoromethyl)hex-3-en-1-yl)benzene

Conditions

Conditions	Yield
With (dppf)Ni(o-tol)Cl; sodium t-butanolate In Hexafluorobenzene at 50℃; for 16h; Inert atmosphere; Schlenk technique; Sealed tube;	99%
With eosin; caesium carbonate In N,N-dimethyl acetamide at 20℃; for 48h; Inert atmosphere; Sealed tube; Irradiation;	87%

: 626-67-5
N-methylcyclohexylamine

: 768-56-9
4-Phenyl-1-butene

: N-(2-methyl-4-phenylbutyl)piperidine

Conditions

Conditions	Yield
With tetrabenzyl titanium; trityl tetrakis(pentafluorophenyl)borate In toluene at 28℃; for 96h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	99%

: 67-56-1
methanol

: 201230-82-2
carbon monoxide

: 768-56-9
4-Phenyl-1-butene

: 131156-36-0
dimethyl 2-(2-phenylethyl)succinate

Conditions

Conditions	Yield
With oxygen; copper(l) chloride; palladium dichloride at 25℃; under 760 Torr; for 60h;	98%
With copper(l) chloride; palladium on activated charcoal at 25℃; under 760 Torr; for 192h;	97%
Stage #1: methanol With palladium(II) trifluoroacetate; bis(9-anthryl)-2,3-dimethyl-1,4-diazabutadiene; toluene-4-sulfonic acid; p-benzoquinone In tetrahydrofuran for 0.166667h; Schlenk technique; Inert atmosphere; Autoclave; Stage #2: carbon monoxide; 4-Phenylbut-1-ene In tetrahydrofuran at 20℃; under 3000.3 Torr; for 66h; Schlenk technique; Inert atmosphere; Autoclave;	77%

...Expand

: 2031-62-1
diethoxymethylane

: 768-56-9
4-Phenyl-1-butene

: 444168-87-0
diethoxy-methyl-(4-phenyl-butyl)-silane

Conditions

Conditions	Yield
Rh(Phebox-ip(S,S))Cl2(H2O) In toluene at 50℃; for 72h;	98%
With C29H35Br2MnN3; sodium t-butanolate In neat (no solvent) at 25℃; Inert atmosphere;	65%

: 768-56-9
4-Phenyl-1-butene

: 25015-63-8
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane

: 167693-07-4
4-phenyl-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)butane

Conditions

Conditions	Yield
Wilkinson's catalyst In dichloromethane 25°C, 10 min;	98%
With 2,6-bis[1-(2,6-diisopropylphenylimino)ethyl]pyridine manganese(II) bromide; sodium t-butanolate In neat (no solvent) at 60℃; for 18h; Inert atmosphere;	93%
With 2,6-bis[1-((2,6-diethylphenyl)imino)ethyl]pyridine; ethylmagnesium bromide; iron(II) chloride In tetrahydrofuran; diethyl ether at 20℃; for 1h; Reagent/catalyst; Solvent; Inert atmosphere;	87%

: 515-84-4
Ethyl trichloroacetate

: 768-56-9
4-Phenyl-1-butene

: 1393712-30-5
C14H17Cl3O2

Conditions

Conditions	Yield
With silicon carbide In chlorobenzene at 200℃; for 1h; Microwave irradiation; regioselective reaction;	98%

: 421-83-0
trifluoromethane sulfonyl chloride

: 768-56-9
4-Phenyl-1-butene

: 1373433-40-9
(3-chloro-5,5,5-trifluoropentyl)benzene

Conditions

Conditions	Yield
With dipotassium hydrogenphosphate; eosin Y disodium In acetonitrile at 20℃; for 12h; Irradiation;	98%
With 2,4,6-trimethyl-pyridine; [Hf6(μ3-OH)4(formato)5.9(eosinato Y)0.1(4'-(4-carboxylatophenyl)[2,2':6',2''-terpyridine]-5,5''-dicarboxylato-Fe(OTf)2)2] In acetonitrile at 20℃; for 2h; Catalytic behavior; Inert atmosphere; Schlenk technique; Irradiation;	86%
With dipotassium hydrogenphosphate; tris(1,10-phenanthroline)ruthenium(II) dichloride In acetonitrile at 25℃; for 15h; Inert atmosphere; Irradiation; regioselective reaction;	81%
With [5,10,15,20-tetraphenylporphyrin]cobalt(III) chloride; Langlois reagent In acetonitrile at 100℃; for 6h; Inert atmosphere; Sealed tube;	51%

: 768-56-9
4-Phenyl-1-butene

: C20H24

Conditions

Conditions	Yield
With (2,6-((2,4,6-tricyclopentyl-C6H2)N-CMe)2C5H3N)Fe(N2) In neat (no solvent) at 23℃; for 24h; Sealed tube; Inert atmosphere; diastereoselective reaction;	98%
With C27H31FeN5 In neat (no solvent) at 23℃; for 48h; Diels-Alder Cycloaddition; stereoselective reaction;

: 768-56-9
4-Phenyl-1-butene

: 2-benzyl-2-methyl-3-morpholino-3-oxopropanal

: 2-benzyl-2-methyl-1-morpholino-7-phenylheptane-1,3-dione

Conditions

Conditions	Yield
With [Rh(bis(dicylohexylphosphino)methane)(C6H5F)][BArF4] In acetone at 55℃; for 18h; Inert atmosphere; Sealed tube; regioselective reaction;	98%

: 768-56-9
4-Phenyl-1-butene

: 694-53-1
phenylsilane

: C16H20Si

Conditions

Conditions	Yield
With 2,6-bis[1-(2,4,6-trimethylimino)ethyl]pyridine; C10H14CoO5 In toluene at 60℃; for 24h; regioselective reaction;	98%
With cobalt(II) tetrafluoroborate hexahydrate; 2,6-bis[1-((2,6-diethylphenyl)imino)ethyl]pyridine In tetrahydrofuran at 20℃; for 4h; regioselective reaction;	78%

: 768-56-9
4-Phenyl-1-butene

: 140681-55-6
Selectfluor

: C17H26ClFN2(2+)*2BF4(1-)

Conditions

Conditions	Yield
With cyclohexenone In acetonitrile for 12h; Inert atmosphere; Microwave irradiation;	98%

: 768-56-9
4-Phenyl-1-butene

: 33626-98-1
methyl 6-bromo-2-naphthoate

: (E)-methyl 6-(4-phenylbut-1-en-1-yl)-2-naphthoate

Conditions

Conditions	Yield
With palladium diacetate; triethylamine; tris-(o-tolyl)phosphine In N,N-dimethyl-formamide at 100℃; for 18h; Heck Reaction; Inert atmosphere;	98%

: 7648-30-8
ethyl 2,2-difluoro-2-iodoacetate

: 768-56-9
4-Phenyl-1-butene

: ethyl 2,2-difluoro-4-iodo-6-phenylhexanoate

Conditions

Conditions	Yield
With diethylzinc In hexane; acetonitrile at -20℃; for 16h; Schlenk technique; Inert atmosphere;	98%

: 768-56-9
4-Phenyl-1-butene

: 1397230-15-7
bis(1-methylethyl) [cyano(diazo)methyl]phosphonate

: bis(1-methylethyl) [1-cyano-2-(2-phenylethyl)cyclopropyl]phosphonate

Conditions

Conditions	Yield
With C44H64O8Rh2 In 1,2-dichloro-ethane at 0 - 20℃; for 16h; stereoselective reaction;	97%

: 92197-18-7
N, N-diisopropyl-O-benzoyl hydroxylamine

: 768-56-9
4-Phenyl-1-butene

: 1372405-11-2
N,N-diisopropyl-4-phenylbutan-1-amine

Conditions

Conditions	Yield
With diethoxymethylane; copper diacetate; 5,5′-bis[di(3,5-di-tert-butyl-4-methoxyphenyl)phosphino]-4,4′-bi-1,3-benzodioxole In tetrahydrofuran at 40℃; for 36h; Glovebox; regioselective reaction;	97%

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