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:19853-09-9
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
Cas:19853-09-9
Min.Order:1 Kilogram
FOB Price: $139.0 / 210.0
Type:Trading Company
inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
Cas:19853-09-9
Min.Order:0
Negotiable
Type:Lab/Research institutions
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
Cas:19853-09-9
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryZhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed
Cas:19853-09-9
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
inquiryHangzhou Fandachem Co.,Ltd, a China-based chemical company, specialize in exporting 2-Phenylbenzyl Bromide, CAS:19853-09-9 Please contact us by email freely. We are leading exporter of 2-Phenylbenzyl Bromide, CAS:19853-09-9 in China
Cas:19853-09-9
Min.Order:1 Metric Ton
Negotiable
Type:Other
inquiryProduct Name: 2-PHENYLBENZYL BROMIDE Synonyms: 2-PHENYLBENZYL BROMIDE;2-(BROMOMETHYL)BIPHENYL;2-(BroMoMethyl)-1,1'-biphenyl;2-Phenylbenzyl broMide 97% CAS: 19853-09-9 MF: C13H11Br MW: 247.13 EINECS: Product Categories: Mol File: 19853-09
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
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
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
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:Beijing or Guangzhou
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
Cas:19853-09-9
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryGood Quality Package:1kg/bag Application:Medical or chemical Transportation:Air/Train/Sea Port:Shenzhen
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Henan Sunlake Enterprise Corporation Our Advantages 1, Any inquiry about ch
2-Phenylbenzyl bromide is a halogenated hydrocarbon. Package:5, 25 g in glass bottle Application:2-Phenylbenzyl bromide may be used in the synthesis of a parent skeleton of 9H-fluorene.
2-biphenylmethanol
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
With hydrogen bromide for 21h; Heating; | 96.6% |
With carbon tetrabromide; triphenylphosphine In acetonitrile at 0 - 20℃; for 0.5h; | 55% |
With phosphorus tribromide |
2-methylbiphenyl
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide; N-Bromosuccinimide In cyclohexane at 50℃; for 4h; Reagent/catalyst; Temperature; | 96.5% |
With tert.-butylhydroperoxide; N-Bromosuccinimide In cyclohexane at 42 - 45℃; for 2h; Green chemistry; | 91.2% |
With N-Bromosuccinimide In tetrachloromethane for 3h; Irradiation; | 85% |
2-methylbiphenyl
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
With N-Bromosuccinimide In nitrogen; water; chlorobenzene | 86% |
phenylboronic acid
1-Bromo-2-bromomethyl-benzene
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium carbonate In 1,4-dioxane at 100℃; for 3h; | 79% |
With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium carbonate In 1,4-dioxane at 100℃; for 3h; Suzuki Coupling; | 79% |
2-biphenylmethanol
o-bromobenzyl alcohol
A
2-phenylbenzyl bromide
B
1-Bromo-2-bromomethyl-benzene
Conditions | Yield |
---|---|
With bromine; triphenylphosphine In dichloromethane at -78 - 20℃; for 18h; Inert atmosphere; | A 75% B 10% |
2-biphenylmethanol
A
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
With hydrogen bromide |
biphenyl-2-carboxylic acid methyl ester
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 98.7 percent / LAH / diethyl ether 2: 96.6 percent / 48percent HBr / 21 h / Heating View Scheme |
biphenyl-2-carbonitrile
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: nickel / 120 - 130 °C / 11400 - 15200 Torr / Hydrogenation 2: sodium nitrite; acetic acid 3: hydrobromic acid / 100 °C View Scheme |
2-phenylbenzylamine
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium nitrite; acetic acid 2: hydrobromic acid / 100 °C View Scheme | |
Multi-step reaction with 2 steps 1: NaNO2; aqueous acetic acid 2: PBr3 View Scheme |
biphenyl-2-ylmagnesium iodide
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: diethyl ether; benzene 2: aqueous HBr View Scheme |
2-Biphenylcarboxylic acid
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: LiAlH4 2: aq. HBr View Scheme |
phenylboronic acid
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: palladium diacetate; sodium carbonate / water; N,N-dimethyl-formamide / 20 °C 2: sodium tetrahydroborate / methanol / 0 - 20 °C 3: triphenylphosphine; carbon tetrabromide / acetonitrile / 20 °C View Scheme | |
Multi-step reaction with 2 steps 1: palladium diacetate; sodium carbonate / water; N,N-dimethyl-formamide / 20 h / 0 - 20 °C / Inert atmosphere 2: carbon tetrabromide; triphenylphosphine / acetonitrile / 0.5 h / 0 - 20 °C View Scheme |
ortho-bromobenzaldehyde
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: palladium diacetate; sodium carbonate / water; N,N-dimethyl-formamide / 20 °C 2: sodium tetrahydroborate / methanol / 0 - 20 °C 3: triphenylphosphine; carbon tetrabromide / acetonitrile / 20 °C View Scheme |
2-Phenylbenzaldehyde
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium tetrahydroborate / methanol / 0 - 20 °C 2: triphenylphosphine; carbon tetrabromide / acetonitrile / 20 °C View Scheme | |
Multi-step reaction with 2 steps 1: sodium tetrahydroborate; methanol / 0.5 h / 0 - 20 °C 2: phosphorus tribromide / dichloromethane / 1 h / 20 °C View Scheme |
o-bromobenzyl alcohol
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: palladium diacetate; sodium carbonate / water; N,N-dimethyl-formamide / 20 h / 0 - 20 °C / Inert atmosphere 2: carbon tetrabromide; triphenylphosphine / acetonitrile / 0.5 h / 0 - 20 °C View Scheme |
bromobenzene
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: magnesium / tetrahydrofuran / 3 h / Reflux 1.2: 50 - 55 °C 2.1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 5 h / 90 °C View Scheme |
2-methylphenyl bromide
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: magnesium / tetrahydrofuran / 3 h / Reflux 1.2: 50 - 55 °C 2.1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 5 h / 90 °C View Scheme |
2-phenylbenzyl bromide
ethyl 4-(piperazin-1-yl)benzoate
4-(4-biphenyl-2-ylmethyl-piperazin-1-yl)-benzoic acid ethyl ester
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In 1,4-dioxane at 40℃; for 0.25h; | 100% |
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
In tetrahydrofuran; N,N-dimethyl-formamide | 100% |
2-phenylbenzyl bromide
o-(iodomethyl)biphenyl
Conditions | Yield |
---|---|
With sodium iodide In acetone at 20℃; for 3h; Inert atmosphere; Darkness; | 100% |
2,2,6,6-Tetramethyl-1-piperidinyloxy free radical
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
Stage #1: 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical With naphthalene; sodium In tetrahydrofuran at 20℃; Stage #2: 2-phenylbenzyl bromide With 1,3-dimethyl-2-imidazolidinone In tetrahydrofuran at 20℃; for 0.5h; | 99% |
2-phenylbenzyl bromide
[1,1'-biphenyl]-2-ylmethanethiol
Conditions | Yield |
---|---|
Stage #1: 2-phenylbenzyl bromide With potassium carbonate; tiolacetic acid In tetrahydrofuran at 20℃; for 0.5h; Stage #2: With methanol In tetrahydrofuran at 20℃; for 0.5h; | 99% |
Multi-step reaction with 2 steps 1: alcohol 2: diluted KOH-solution View Scheme | |
Multi-step reaction with 2 steps 1: acetone / Reflux 2: acetyl chloride / methanol / 2 h / 20 °C View Scheme |
2-phenylbenzyl bromide
phenyltriisopropoxytitanium(IV)
2-benzyl-1,1'-biphenyl
Conditions | Yield |
---|---|
With palladium diacetate; Tri(p-tolyl)phosphine In toluene at 25℃; for 2h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
In 1,4-dioxane; ethanol; water Reflux; | 99% |
2-phenylbenzyl bromide
sodium [13C]cyanide
2-biphenylacetonitrile-1-13C
Conditions | Yield |
---|---|
In dimethyl sulfoxide | 98.8% |
2-phenylbenzyl bromide
trimethylamine
1-([1,1′-biphenyl]-2-yl)-N,N,N-trimethylmethanaminium bromide
Conditions | Yield |
---|---|
In ethyl acetate at 32℃; for 3h; | 98% |
In ethyl acetate at 40℃; for 5h; | 97.1% |
2-phenylbenzyl bromide
1,2-bis(biphenyl-2-yl)ethane
Conditions | Yield |
---|---|
With potassium phosphate; (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis-(2-phenylpyridine(-1H))-iridium(III) hexafluorophosphate; diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate In N,N-dimethyl-formamide at 20℃; for 4h; Inert atmosphere; Irradiation; | 98% |
1H-imidazole
2-phenylbenzyl bromide
1-biphenyl-2-ylmethyl-1H-imidazole
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 120℃; for 2h; | 96% |
Conditions | Yield |
---|---|
In acetone Reflux; | 96% |
2-phenylbenzyl bromide
triethylamine
1-([1,1′-biphenyl]-2-yl)-N,N,N-trimethylmethanaminium bromide
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 1h; | 95% |
2-phenylbenzyl bromide
1-(2,4,6-trimethylbenzyl)-4,5-dihydroimidazole
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 8h; | 94% |
(11aS)-(+)-10-di(p-anisyl)methyl-2,3,5,10,11,11a-hexahydro-5,11-dioxo-1H-pyrrolo[2,1-c][1,4]benzodiazepine
2-phenylbenzyl bromide
(11aR)-(+)-10-di(p-anisyl)methyl-2,3,5,10,11,11a-hexahydro-5,11-dioxo-11a-(2-phenyl)benzyl-1H-pyrrolo[2,1-c][1,4]benzodiazepine
Conditions | Yield |
---|---|
Stage #1: (11aS)-(+)-10-di(p-anisyl)methyl-2,3,5,10,11,11a-hexahydro-5,11-dioxo-1H-pyrrolo[2,1-c][1,4]benzodiazepine; 2-phenylbenzyl bromide With N,N,N,N,N,N-hexamethylphosphoric triamide In tetrahydrofuran at -100℃; for 0.25h; Stage #2: With potassium hexamethylsilazane In tetrahydrofuran; hexane at -100℃; | 94% |
2-phenylbenzyl bromide
5-[(triphenylmethyl)oxy]pentanol
Conditions | Yield |
---|---|
With tetrabutylammomium bromide In N,N-dimethyl-formamide; mineral oil at 20℃; for 4h; Cooling with ice; | 94% |
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
With lithium hexamethyldisilazane In tetrahydrofuran at -78 - 20℃; for 2h; Inert atmosphere; | 94% |
2-phenylbenzyl bromide
ethyl acetoacetate
5-biphenyl-2-yl-3-oxo-pentanoic acid ethyl ester
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 93% |
tert-butyl 4-[(2,2-dimethylpropyl)amino]piperidine-1-carboxylate
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20℃; | 93% |
2-phenylbenzyl bromide
(3S)-3-methyl-3-vinylisoindolin-1-one
(3S)-2-(biphenyl-2-ylmethyl)-3-methyl-3-vinylisoindolin-1-one
Conditions | Yield |
---|---|
Stage #1: (3S)-3-methyl-3-vinylisoindolin-1-one With sodium hydride In tetrahydrofuran; mineral oil at 20℃; for 0.0833333h; Stage #2: 2-phenylbenzyl bromide In tetrahydrofuran at 20 - 60℃; | 93% |
2-phenylbenzyl bromide
(R)-1-phenyl-ethyl-amine
Conditions | Yield |
---|---|
With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; sodium carbonate at 100℃; for 2.5h; | 92% |
1-(1-methyl-1H-imidazol-2-yl)-2-(naphthalen-2-ylmethoxy)ethanone
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
With cesium hydroxide In hexane; dichloromethane at -40℃; for 20h; | 92% |
2-phenylbenzyl bromide
(S)-1-phenyl-ethylamine
Conditions | Yield |
---|---|
With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; sodium carbonate at 100℃; for 2.5h; | 91% |
2-phenylbenzyl bromide
1-(2-methoxyethyl)-4,5-dihydroimidazole
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 8h; | 91% |
Conditions | Yield |
---|---|
Stage #1: 2-phenylbenzyl bromide; Diethyl methylmalonate With sodium In ethanol at 130℃; for 3h; Stage #2: With potassium hydroxide In tetrahydrofuran; water at 100℃; for 4h; | 91% |
2-phenylbenzyl bromide
N,N-dimethyl (trimethylsilyl)methanamide
Conditions | Yield |
---|---|
tetrakis(triphenylphosphine) palladium(0) In toluene at 65℃; for 0.75h; | 90% |
2-phenylbenzyl bromide
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20℃; | 90% |
With potassium carbonate In acetonitrile at 20℃; | 90% |
With potassium carbonate In acetonitrile at 20℃; | 90% |
With potassium carbonate In acetonitrile at 20℃; | 90% |
N,N-(2-hydroxy-4-nitrophenyl)dimethanesulfonamide
2-phenylbenzyl bromide
N,N-[2-(2'-phenylbenzyloxy)-4-nitrophenyl]-dimethanesulfonamide
Conditions | Yield |
---|---|
With potassium carbonate | 90% |
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