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:27976-27-8
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryTIANFUCHEM--27976-27-8--1-BROMO-6-PHENYLHEXANE in stock Our company was built in 2009 with an ISO certificate.In the past 10 years, we have grown up as a famous fine chemicals supplier in China And we had established stable business re
Cas:27976-27-8
Min.Order:1 Metric Ton
FOB Price: $2000.0
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
Cas:27976-27-8
Min.Order:0 Metric Ton
Negotiable
Type:Other
inquiryJ&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,stable supply chain.Appearance:white/off-white or light yellow Storage:Store in cool and dry place, keep away from strong light and heat. Package:aluminum bottle,glass bottle,PTFE bottle,cardboard drum Application:This product can be use
R & D enterprises have their own stock in stockAppearance:To be subject to the object Package:Customized Application:pharmaceutical intermediates Transportation:Air Port:Shanghai;Guangzhou
Shanghai Finebiotech Co.,Ltd.was established in 2020, which providing professional chemical services. As a customer-oriented company, we have distinguished ourself from others in providing worldwide customers with cost-effective and efficient service
1-bromo-6-phenylhexaneAppearance:detailed see specifications Storage:Keep away of light, cool place Package:25kg/drum;200kg/drum Application:An important raw material and intermediate used in Organic Synthesis, Pharmaceuticals Transportation:Sea/air/
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:27976-27-8
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiryBefore-Sale Service:---Any inquiries will be replied within 12 hours.---Golden Manufactory under?ISO/GMP?with?large stock.---Dedication to quality,We?have?strict?quality?control?system.?---OEM/ODM Available.---Sample is available for your evaluation
Price, service, company and transport advantage: 1. Best service, place of origin China, high quality, and reasonable price. 2. It's customers' right to choose the package (EMS, DHL, FEDEX, UPS). 3. It's customers' right
Cas:27976-27-8
Min.Order:0
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Type:Trading Company
inquiryYinghao 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
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
1. Production capacity: we have three production base with high-tech production equipment and instruments, equipped with professional production personnel, meet your requirements.2. Quality assurance: we have a first-class testing equipment and testi
Shanghai, Run-Biotech Co., Ltd is a leading domestic pharmaceutical, biopharmaceutical, and health care products R & D outsourcing services company. As an innovation-driven and customer-focused company, Run Biotech provides a broad and integrated por
FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the 1-BROMO-6-PHENYLHEXANE, CAS:27976-27-8 with the most competitive price and the best q
R & D enterprises have their own stock in stockAppearance:To be subject to the object Package:Customized Application:pharmaceutical intermediates Transportation:Air Port:Shanghai;Guangzhou
Adequate stocks available,prompt shipment,Strictly control on quality,Timely after-sales
Cas:27976-27-8
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryDebyesci 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
High quality Products with prompt delivery Package:based on customer requirement Application:organic intermediates Transportation:By air or By sea Port:any port or China
6-phenyl-1-hexanol
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
With carbon tetrabromide; triphenylphosphine In dichloromethane for 1h; | 77% |
With phosphorus tribromide In diethyl ether at 0 - 20℃; for 15h; | 34% |
With phosphorus; sulfuric acid; hydrogen bromide |
Conditions | Yield |
---|---|
In tetrahydrofuran; diethyl ether; hexane at -14 - 20℃; for 7h; Inert atmosphere; | 70% |
In tetrahydrofuran | |
In tetrahydrofuran; diethyl ether at -10℃; for 0.5h; |
A
1,6-diphenylhexane
B
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
With buta-1,3-diene; palladium(II) acetylacetonate In tetrahydrofuran at 20℃; for 3h; | A 8% B 69% |
With buta-1,3-diene; nickel dichloride In tetrahydrofuran at 20℃; for 3h; | A 20% B 27% |
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[2.2.2.]octane; (1,2,3,4,5-pentamethyl-cyclopenta-2,4-dienylmethyl)PPh2*BH3; nickel dichloride In tetrahydrofuran; diethyl ether; toluene at 25℃; for 3h; | 68% |
1 ,6-dibromohexane
benzene
A
(5-bromo-1-methylpentyl)benzene
B
1,2,3,4-tetrahydro-1,4-dimethylnaphthalene
C
(6-bromohexyl)benzene
D
1-ethyltetralin
Conditions | Yield |
---|---|
With silver trifluoromethanesulfonate for 20h; Heating; Further byproducts given; | A 21% B 24% C 6% D 25% |
5-hexen-2-ylbenzene
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
With hydrogen bromide; dihydrogen peroxide |
6-phenylhexyl acetate
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
With hydrogen bromide Heating; Yield given; | |
With hydrogen bromide Reflux; |
6-phenyl-1-hexene
hydrogen bromide
(6-bromohexyl)benzene
(E/Z)-6-Phenylhex-5-enoic acid
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: diethyl ether; methanol 2: DIBAL-H / CH2Cl2 / 0.5 h / 0 °C 3: H2 / PtO2 / methanol / 2585.7 Torr 4: NBS, Ph3P / CH2Cl2 / 0.42 h / 0 - 20 °C View Scheme |
(4-carboxybutyl)triphenylphosphonium bromide
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: 1.) NaCH2SOCH3 / 1.) DMSO, RT, 30 min, 2.) DMSO, RT, 1 h 2: diethyl ether; methanol 3: DIBAL-H / CH2Cl2 / 0.5 h / 0 °C 4: H2 / PtO2 / methanol / 2585.7 Torr 5: NBS, Ph3P / CH2Cl2 / 0.42 h / 0 - 20 °C View Scheme |
6-phenylhex-5-en-1-ol
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: H2 / PtO2 / methanol / 2585.7 Torr 2: NBS, Ph3P / CH2Cl2 / 0.42 h / 0 - 20 °C View Scheme |
benzaldehyde
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: 1.) NaCH2SOCH3 / 1.) DMSO, RT, 30 min, 2.) DMSO, RT, 1 h 2: diethyl ether; methanol 3: DIBAL-H / CH2Cl2 / 0.5 h / 0 °C 4: H2 / PtO2 / methanol / 2585.7 Torr 5: NBS, Ph3P / CH2Cl2 / 0.42 h / 0 - 20 °C View Scheme |
(E)-6-phenyl-5-hexenoic acid methyl ester
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: DIBAL-H / CH2Cl2 / 0.5 h / 0 °C 2: H2 / PtO2 / methanol / 2585.7 Torr 3: NBS, Ph3P / CH2Cl2 / 0.42 h / 0 - 20 °C View Scheme |
6-phenyl-hexanoic acid methyl ester
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: LiBH4 2: sulfuric acid; red phosphorus; aqueous hydrobromic acid View Scheme |
2,3-dichlorotetrahydro-2H-pyran
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: (i) Mg, Et2O, (ii) Na 2: H2 / Raney-Ni 3: aq. HBr, H2SO4 View Scheme | |
Multi-step reaction with 2 steps 2: aq. HBr View Scheme |
trans-6-phenyl-4-hexen-1-ol
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: H2 / Raney-Ni 2: aq. HBr, H2SO4 View Scheme |
benzyl chloride
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: (i) Mg, Et2O, (ii) Na 2: H2 / Raney-Ni 3: aq. HBr, H2SO4 View Scheme |
benzylmagnesium chloride
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: aq. HBr View Scheme |
Conditions | Yield |
---|---|
With triphenylphosphine In dichloromethane | |
With triphenylphosphine In dichloromethane | |
With triphenylphosphine In dichloromethane |
(6-bromohexyl)benzene
6-bromohexanoyl chloride
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
With triethylsilane; aluminium chloride In hexane; dichloromethane; water; benzene |
1-phenyl-2-bromoethane
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: iodine; magnesium / tetrahydrofuran / Inert atmosphere; Reflux 1.2: 1 h / 5 - 10 °C / Inert atmosphere 2.1: hydrogen bromide / Reflux View Scheme |
Conditions | Yield |
---|---|
With n-butyllithium In diethyl ether; hexane at 0℃; for 2h; Inert atmosphere; |
Conditions | Yield |
---|---|
With Cl2CuI(2-)*2Li(1+) In tetrahydrofuran at 20℃; for 2h; |
benzyl boronic acid
5-bromopentyl trifluoromethanesulfonate
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
With potassium phosphate In toluene at 60℃; for 12h; | 13 mg |
5-bromopentan-1-ol
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 2,6-dimethylpyridine / dichloromethane / 0.33 h / -78 °C / Inert atmosphere 2: potassium phosphate / toluene / 12 h / 60 °C View Scheme |
2-Phenylethyl cyclopropyl carbinol
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: lithium bromide; phosphorus tribromide; zinc dibromide View Scheme |
Conditions | Yield |
---|---|
With triethylsilane; aluminium chloride In hexane; dichloromethane; water; benzene |
(6-bromohexyl)benzene
6-phenyl-1-hexyl iodide
Conditions | Yield |
---|---|
In acetone | 99% |
With sodium iodide In acetone | 99% |
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
With sodium sulfite In ethanol; water for 24h; Heating; | 96% |
With sodium sulfite In tetrahydrofuran; ethanol; water at 160℃; for 0.25h; Microwave irradiation; |
(6-bromohexyl)benzene
6-phenylhexane-1-thiol
Conditions | Yield |
---|---|
Stage #1: (6-bromohexyl)benzene With hexamethyldisilathiane; tetrabutyl ammonium fluoride In tetrahydrofuran at -20 - 20℃; for 12h; Darkness; Stage #2: With ammonium chloride In dichloromethane; water | 91% |
Multi-step reaction with 2 steps 1: 0.48 g / NaOH View Scheme | |
With ammonia; thiourea In ethanol; dichloromethane |
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 70℃; for 24h; Inert atmosphere; Sealed tube; | 85% |
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide for 10h; Heating; | 81% |
(6-bromohexyl)benzene
hexylbenzene
Conditions | Yield |
---|---|
With n-butyllithium; samarium diiodide; dipyrrolidinomethylaminophosphoric acid triamide; tert-butyl alcohol In tetrahydrofuran; hexane at -66 - 21℃; | 80% |
4-[2-(4-benzyloxyphenyl)-5-methyl-1H-pyrrol-1-yl]phenol
(6-bromohexyl)benzene
2-(4-Benzyloxyphenyl)-5-methyl-1-[4-(6-phenylhexyloxy)-phenyl]-1H-pyrrole
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide | 79.4% |
Conditions | Yield |
---|---|
With triethylamine In acetonitrile for 15h; Reflux; | 77% |
4-phenyl-4-cyanopiperidine
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
75% |
(6-bromohexyl)benzene
4-Piperazin-1-yl-pyrrolo[1,2-a]quinoxaline
Conditions | Yield |
---|---|
With triethylamine In acetonitrile Reflux; | 75% |
Conditions | Yield |
---|---|
With sodium hydroxide In dimethyl sulfoxide at 100℃; for 5h; Etherification; | 72% |
7-hydroxy-8-nitrochromone
(6-bromohexyl)benzene
8-nitro-7-<(6-phenylhexyl)oxy>chromone
Conditions | Yield |
---|---|
With potassium carbonate; lithium iodide In N,N-dimethyl-formamide at 90℃; for 24h; | 68% |
4-{2-[2-(4-benzyloxyphenyl)-5-methyl-1H-pyrrol-1-yl]ethyl}phenol
(6-bromohexyl)benzene
2-(4-benzyloxyphenyl)-5-methyl-1-{2-[4-(6-phenylhexyloxy)phenyl]ethyl}-1H-pyrrole
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide | 67.1% |
phenyl sulfamate
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
Stage #1: phenyl sulfamate; (6-bromohexyl)benzene With aluminum oxide; tert-butyl isocyanide; bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]} for 0.166667h; Stage #2: With (PhI(OtBu)2) for 6h; Sealed tube; | 65% |
Dichloromethyl methyl ether
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
With titanium tetrachloride In dichloromethane at 35℃; for 1h; Cooling with ice; | 60% |
With titanium tetrachloride In dichloromethane at 0 - 35℃; for 0.666667h; |
methyl 5-(furan-2-yl)-1,3,4-oxadiazole-2-carboxylate
(6-bromohexyl)benzene
Conditions | Yield |
---|---|
Stage #1: (6-bromohexyl)benzene With magnesium In tetrahydrofuran; ethylene dibromide at 23℃; Grignard reaction; Inert atmosphere; Sonication; Stage #2: methyl 5-(furan-2-yl)-1,3,4-oxadiazole-2-carboxylate In tetrahydrofuran; ethylene dibromide at -40℃; for 2h; | 57% |
methyl 5-(thiophen-2-yl)-1,3,4-oxadiazole-2-carboxylate
(6-bromohexyl)benzene
7-phenyl-1-(5-(thien-2-yl)-1,3,4-oxadiazol-2-yl)-heptan-1-one
Conditions | Yield |
---|---|
Stage #1: (6-bromohexyl)benzene With magnesium In tetrahydrofuran; ethylene dibromide at 23℃; Grignard reaction; Inert atmosphere; Sonication; Stage #2: methyl 5-(thiophen-2-yl)-1,3,4-oxadiazole-2-carboxylate In tetrahydrofuran; ethylene dibromide at -40℃; for 2h; | 57% |
(+/-)-5-benzyl-5-ethyl-4-oxo-1,2-oxathiolane-2,2-dioxide
(6-bromohexyl)benzene
(+/-)-5-benzyl-5-ethyl-4-(6'-phenylhexyloxy)-5H-1,2-oxathiole-2,2-dioxide
Conditions | Yield |
---|---|
With tetra-(n-butyl)ammonium iodide; potassium carbonate In acetonitrile at 40℃; for 4h; | 56% |
methyl 3-(6-bromopyridin-2-yl)-1,2,4-oxadiazole-5-carboxylate
(6-bromohexyl)benzene
1-(3-(6-bromopyridin-2-yl)-1,2,4-oxadiazol-5-yl)-7-phenylheptan-1-one
Conditions | Yield |
---|---|
Stage #1: (6-bromohexyl)benzene With magnesium In tetrahydrofuran; ethylene dibromide at 23℃; Grignard reaction; Inert atmosphere; Sonication; Stage #2: methyl 3-(6-bromopyridin-2-yl)-1,2,4-oxadiazole-5-carboxylate In tetrahydrofuran; ethylene dibromide at -40℃; for 2h; | 55% |
(6-bromohexyl)benzene
dimethyl amine
N,N-dimethyl-6-phenylhexylamine
Conditions | Yield |
---|---|
In tetrahydrofuran; diethyl ether for 50h; Ambient temperature; | 51% |
(6-bromohexyl)benzene
methyl 5-(pyridin-2-yl)-1,3,4-oxadiazole-2-carboxylate
Conditions | Yield |
---|---|
Stage #1: (6-bromohexyl)benzene With magnesium In tetrahydrofuran; ethylene dibromide at 23℃; Grignard reaction; Inert atmosphere; Sonication; Stage #2: methyl 5-(pyridin-2-yl)-1,3,4-oxadiazole-2-carboxylate In tetrahydrofuran; ethylene dibromide at -40℃; for 2h; | 51% |
Stage #1: (6-bromohexyl)benzene With magnesium; ethylene dibromide In tetrahydrofuran at 23℃; Inert atmosphere of Ar; Heating; Sonication; Stage #2: methyl 5-(pyridin-2-yl)-1,3,4-oxadiazole-2-carboxylate In tetrahydrofuran at -40℃; for 2h; | 51% |
Stage #1: (6-bromohexyl)benzene With iodine; magnesium In tetrahydrofuran at 60℃; for 2h; Stage #2: methyl 5-(pyridin-2-yl)-1,3,4-oxadiazole-2-carboxylate In tetrahydrofuran at -40℃; for 4h; | 51% |
(6-bromohexyl)benzene
p-aminoethylbenzoate
ethyl 4-(6-phenylhexylamino)benzoate
Conditions | Yield |
---|---|
In N,N,N,N,N,N-hexamethylphosphoric triamide at 125℃; for 24h; | 50% |
Conditions | Yield |
---|---|
With potassium fluoride; benzylnixantphos; iron(II) acetate In tetrahydrofuran at 0 - 40℃; for 12h; Negishi Coupling; Inert atmosphere; | 50% |
(6-bromohexyl)benzene
triphenylphosphine
Conditions | Yield |
---|---|
With potassium iodide In acetonitrile at 85℃; | 43% |
(6-bromohexyl)benzene
5-methyl-4-mercaptomethylimidazole hydrochloride
5-Methyl-4-(6-phenyl-hexylsulfanylmethyl)-1H-imidazole
Conditions | Yield |
---|---|
With N-benzyl-N,N,N-triethylammonium chloride In water; isopropyl alcohol at 80℃; for 4h; | 41% |
dibenzyl methylphosphonate
(6-bromohexyl)benzene
dibenzyl 6-phenylhexylphosphonate
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran; hexane at -78 - 20℃; | 38.5% |
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