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Cas:100-39-0
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inquiryWelcome 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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inquiryProduct Description Name Benzyl bromide CAS 100-39-0 Assay 99% Appearance Colorless to yellowish liquid Capacity 500mt/year Min.package 100gram Standard Enterprise e
Cas:100-39-0
Min.Order:1 Kilogram
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inquiryhigh quality Appearance:white powder Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai
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
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
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
Cas:100-39-0
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inquiry1. Best prices with satisfied quality; 2. It's clients' right to choose the package's Courier (EMS, DHL, FedEx, UPS); 3.It's clients' right to choose the packing way for his produccts from many recent effective packing ways;
Benzyl bromide Basic information Product Name: Benzyl bromide Synonyms: (bromomethyl)-benzen;1-Bromotoluene;ai3-15300;alpha-bromo-toluen;Bromophenylmethane;-Bromotoluene;Bromotoluene, alpha;bromotoluene,alpha CAS: 100-39-0 MF: C7H7Br MW: 171.0
Cas:100-39-0
Min.Order:1 Kilogram
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inquiryMinimum Order Qty. 10 Gram Supply Ability 500 Kilograms/Month Storage store in cool, dry, ventilated place 20℃ Delivery Time 3 business days after payment Payment Term TT,western union,Paypal,MoneyGram Package 10g,20g,50g,100g,500g,1KGS,
Cas:100-39-0
Min.Order:10 Gram
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inquiryHigh qualityHangzhou Keying Chem Co., Ltd. Is a comprehensive enterprise, dedicated to the development, production and marketing of chemicals. As a technology innovative and service professional enterprise, Our company mainly engages in global phar
Cas:100-39-0
Min.Order:1 Gram
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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
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:100-39-0
Min.Order:10 Gram
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inquirySuperior quality Appearance:Clear light amber liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Used as Pharmaceutical Intermediates Transpor
Product Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
Cas:100-39-0
Min.Order:1 Kilogram
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inquiryWe are leading fine chemicals supplier in China with ISO certificate, Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED
Cas:100-39-0
Min.Order:1 Gram
FOB Price: $3.0
Type:Lab/Research institutions
inquirySupply good price100-39-0 Benzyl bromide with high quality guarenteed Located in Hangzhou National Hi-Tech Industrial Development Zone, zhongqichem is a technical company mainly focus on the Custom synthesis, manufacturing, sales of chemicals to
Cas:100-39-0
Min.Order:1 Gram
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Type:Other
inquiryHangzhou 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
Appearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
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
high purity,in stock Package:25kg/drum,or as per customers'demand Application:API,or Intermediates,fine chemicals Transportation:air,sea,courier
Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
Best service,high quality and cheap price. Storage:Keep away from heat,sparks and flames. Package:25kg/50kg/200kg drum or Customer demand Application:Used as pharmaceutical intermediates Transportation:BY sea/air or by courier
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Hangzhou ZeErRui Chemical Co., Ltd. located in Lingang industrial areas, our plant covers an area of 6000 square meters.ZeErRui dedicated to the development, production and marketing of chemicals. We have earned ourselves a good reputation at home
Cas:100-39-0
Min.Order:0 Metric Ton
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Type:Lab/Research institutions
inquiryProduct Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:100-39-0
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
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Conditions | Yield |
---|---|
With bromine In tetrachloromethane for 1.5h; Ambient temperature; | 100% |
With manganese(IV) oxide; bromine In dichloromethane at 0℃; for 1h; Product distribution; Further Variations:; Solvents; Temperatures; reaction time; | 100% |
With bromine; sodium t-butanolate In cyclohexane Heating; | 100% |
Conditions | Yield |
---|---|
With 1,1,1,2,2,2-hexamethyldisilane; pyridinium hydrobromide perbromide In chloroform at 25℃; for 0.5h; | 100% |
With phosphorus tribromide In benzene at 20℃; | 100% |
Stage #1: benzyl alcohol With 1,2,3-Benzotriazole; thionyl chloride In dichloromethane for 0.0833333h; Stage #2: With potassium bromide In dichloromethane; N,N-dimethyl-formamide for 0.5h; | 99% |
benzyl bromide
Conditions | Yield |
---|---|
With bromine In acetonitrile one-electron oxidn. of cis-Co complex by Br2 at 298 K; monitored by (1)H-NMR; | 100% |
C13H25N3PS(1+)
benzyl bromide
Conditions | Yield |
---|---|
With bromide In N,N-dimethyl-formamide | 98% |
Conditions | Yield |
---|---|
With Dichloromethylsilane; phosphorus tribromide; iron(III) chloride In acetonitrile for 4h; Heating; | 97% |
With polymethylhydrosiloxane; dimethylbromosulphonium bromide In chloroform at 20℃; for 5h; | 96% |
With chloro-trimethyl-silane; 1,1,3,3-Tetramethyldisiloxane; lithium bromide In acetonitrile at 80℃; for 30h; | 94% |
Conditions | Yield |
---|---|
With bismuth(III) bromide In 1,2-dichloro-ethane at 25℃; for 2.25h; | 97% |
With pyridine; tributyltin bromide at 50℃; Thermodynamic data; Equilibrium constant; other temperatures, Δ G; | 26 % Spectr. |
Conditions | Yield |
---|---|
With triethylsilane; Acetyl bromide; tin(II) bromide In dichloromethane for 3h; Ambient temperature; | 96% |
Conditions | Yield |
---|---|
With 4-aminophenyl diphenylphosphinite; N-Bromosuccinimide In dichloromethane at 20℃; for 2h; | 95% |
With boron trifluoride diethyl etherate; lithium bromide In acetonitrile for 24h; Ambient temperature; | 89% |
With 1-(2-OPPh2-propyl)-3-methylimidazolium hexafluorophosphate; bromine at 80℃; for 2h; | 89% |
Conditions | Yield |
---|---|
With hydrogen bromide at 130℃; for 1h; | 95% |
Multi-step reaction with 2 steps 1: 12 N HCl / 105 °C 2: 93 percent / 47percent aq. HBr / 1 h / 130 °C View Scheme |
benzyloxy-trimethylsilane
benzyl bromide
Conditions | Yield |
---|---|
With 4-aminophenyl diphenylphosphinite; bromine In dichloromethane at 20℃; | 95% |
With 1-(2-OPPh2-propyl)-3-methylimidazolium hexafluorophosphate; bromine at 80℃; for 1h; | 87% |
With Tri-n-butylfluorphosphoniumbromid In benzene at 20℃; for 24h; | 81% |
benzyl mesylate
benzyl bromide
Conditions | Yield |
---|---|
With 1-n-butyl-3-methylimidazolim bromide at 50℃; for 1h; Inert atmosphere; Green chemistry; | 95% |
With lithium bromide In tetrahydrofuran at 20℃; for 2h; Inert atmosphere; | 89% |
With calcium bromide In dimethyl sulfoxide for 3h; Ambient temperature; | 79% |
3,5-dimethoxy-4-methylphenylmethyl alcohol
A
5-(bromomethyl)-1,3-dimethoxy-2-methylbenzene
B
benzyl bromide
Conditions | Yield |
---|---|
With phosphorus tribromide | A n/a B 95% |
Conditions | Yield |
---|---|
With water; boron tribromide In chloroform-d1 at 20℃; Solvent; | A 95% B 88% |
Conditions | Yield |
---|---|
With calcium bromide; tetrahexylammonium bromide at 110℃; for 24h; | 94% |
With hydrogen bromide at 130℃; for 1h; | 93% |
With 1-bromo-butane; Mg6Al2(OH)16Cl2*4H2O In N,N-dimethyl-formamide at 69.9℃; for 20h; | 90% |
Conditions | Yield |
---|---|
With Silphos; bromine In acetonitrile for 0.166667h; Heating; | 92% |
With N-Bromosuccinimide; triphenylphosphine In dichloromethane at 20℃; for 5h; | 72% |
Conditions | Yield |
---|---|
With triethylsilane; Acetyl bromide; tin(II) bromide In dichloromethane for 3h; Ambient temperature; | 91% |
(benzyloxy)(tert-butyl)dimethylsilane
benzyl bromide
Conditions | Yield |
---|---|
With boron tribromide In dichloromethane for 0.166667h; Ambient temperature; | 90% |
Conditions | Yield |
---|---|
With tetrabutylammomium bromide; hydrogen bromide; potassium bromide In water at 20℃; Irradiation; Green chemistry; | A 90% B n/a |
With N-hydroxyphthalimide; carbon tetrabromide; trichloroisocyanuric acid; cobalt(II) diacetate tetrahydrate In dichloromethane at 25℃; for 20h; |
Conditions | Yield |
---|---|
With tetra-N-butylammonium tribromide; dibromoisocyanuric acid In dichloromethane at 20℃; for 2h; UV-irradiation; | 90% |
Conditions | Yield |
---|---|
With triethylsilane; Acetyl bromide; tin(II) bromide In dichloromethane for 3h; Ambient temperature; | 89% |
ammonium acetate
benzyl alcohol
A
Benzyl acetate
B
benzyl bromide
Conditions | Yield |
---|---|
With N-Bromosuccinimide; triphenylphosphine In acetonitrile at 20℃; for 2h; Cooling with ice; | A 87% B 3% |
With bromine; triphenylphosphine In acetonitrile at 20℃; for 0.7h; | A 40% B 53% |
Conditions | Yield |
---|---|
With bromine In dichloromethane for 2h; Ambient temperature; Irradiation; | A 11% B 86% |
With hydrogen bromide; dihydrogen peroxide In water at 20℃; for 10h; Irradiation; | A 4% B 81% |
With hydrogen bromide; dihydrogen peroxide In water at 27℃; for 24h; Irradiation; | A 7% B 81% |
benzyl bromide
Conditions | Yield |
---|---|
Stage #1: 4-[(3,5-bis-trifluoromethyl-benzyl)-methoxycarbonyl-amino]-2-ethyl-piperidine-1-carboxylic acid tert-butyl ester With hydrogenchloride In ethyl acetate for 4.08333h; Stage #2: With water; sodium hydrogencarbonate In ethyl acetate | 84% |
Conditions | Yield |
---|---|
With N-Bromosuccinimide In dichloromethane; benzene Irradiation (UV/VIS); nitrogen atmosphere; mercurial and NBS (2.5 equiv)/CH2Cl2 in deoxygenated solvent irradiated (250-W sunlamp, 40 °C, 6h);; filtration; solvent removed (vacuum); PhCH2CH2Ph and PhCH2Br analysed by (1)H NMR, GLC and GCMS;; | A 84% B 4% |
With N-Bromosuccinimide In dichloromethane; benzene Irradiation (UV/VIS); nitrogen atmosphere; mercurial and NBS (2.5 equiv)/CH2Cl2 in deoxygenated solvent irradiated (250-W sunlamp, 40 °C, 4h) in the presence of 20 mol% (t-Bu)2NO (radical);; filtration; solvent removed (vacuum); PhCH2CH2Ph and PhCH2Br analysed by (1)H NMR, GLC and GCMS;; | A 46% B 2% |
acetic acid
toluene
A
benzyl bromide
B
acetophenone
C
benzoic acid
Conditions | Yield |
---|---|
With hydrogen bromide; oxygen; bromide; cobalt(II) acetate; manganese(II) acetate at 75℃; Kinetics; Product distribution; atmospheric pressure; | A n/a B n/a C 83% |
{(η5-C5Me5)Os(CO)(PMe2Ph)CH2Ph}
bromine
A
{(η5-C5Me5)Os(CO)(PMe2Ph)Br}
B
benzyl bromide
Conditions | Yield |
---|---|
In dichloromethane-d2 (N2); electrophilic cleavage reaction by addn. of bromine to a soln. of Cp*Os(CO)(PMe2Ph)CH2Ph in CD2Cl2;; not isolated, detected by NMR;; | A 77% B 83% |
[(ethoxymethoxy)methyl]benzene
benzyl bromide
Conditions | Yield |
---|---|
With tetrabutylammomium bromide; 1-(n-butyl)-3-methylimidazolium tetrachloroindate at 135 - 140℃; for 0.075h; Microwave irradiation; Neat (no solvent); chemoselective reaction; | 83% |
diethyl 2,6-dimethyl-4-benzyl-1,4-dihydropyridine-3,5-dicarboxylate
benzyl bromide
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; tris(2,2′-bipyridyl)dichlororuthenium(II) hexahydrate; sodium bromide In water; acetonitrile at 20℃; for 24h; Sealed tube; Inert atmosphere; Irradiation; regioselective reaction; | 83% |
Conditions | Yield |
---|---|
100% | |
In acetone; benzene at 20℃; for 24h; | 100% |
In dichloromethane at 20℃; for 12h; | 100% |
1-methyl-1H-imidazole
benzyl bromide
3-benzyl-1-methylimidazolium bromide
Conditions | Yield |
---|---|
at 100℃; for 2h; | 100% |
In 1,4-dioxane at 100℃; for 12h; | 98% |
In ethanol; acetonitrile at 80℃; for 12h; | 98% |
Conditions | Yield |
---|---|
In methanol for 336000h; Heating; | 100% |
In acetone; benzene at 20℃; for 24h; | 100% |
In methanol for 336h; Heating; | 100% |
nicotinamide
benzyl bromide
3-(aminocarbonyl)-1-benzylpyridinium bromide
Conditions | Yield |
---|---|
In acetone for 12h; Reflux; | 100% |
In acetonitrile | 93% |
In acetonitrile at 140℃; for 1.5h; Sealed tube; Microwave irradiation; | 89% |
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide In acetone Heating; | 100% |
With caesium carbonate In acetonitrile at 50℃; | 98% |
With caesium carbonate In acetonitrile at 50℃; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile for 6h; | 100% |
Stage #1: 4-bromo-phenol With sodium hydride In N,N-dimethyl-formamide at 5℃; for 0.333333h; Inert atmosphere; Stage #2: benzyl bromide In N,N-dimethyl-formamide at 20℃; for 2h; Inert atmosphere; | 99% |
With potassium phosphate; tetrabutylammomium bromide In water at 20℃; for 2h; Sealed tube; Green chemistry; | 99% |
Conditions | Yield |
---|---|
In toluene at 95℃; for 4h; | 100% |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 3h; | 100% |
With caesium carbonate In N,N-dimethyl-formamide at 20℃; for 3h; | 87% |
With potassium carbonate In N,N-dimethyl-formamide at 60℃; for 12h; Inert atmosphere; | 48.6% |
3-methyl-2-nitrophenol
benzyl bromide
1-(benzyloxy)-3-methyl-2-nitrobenzene
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile Heating / reflux; | 100% |
With potassium carbonate In acetonitrile at 40 - 75℃; for 7.75h; | 99% |
With potassium carbonate; acetone |
methyl 4-hydroxycinnamate
benzyl bromide
(E)-methyl 3-(4-(benzyloxy)phenyl)acrylate
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 23℃; for 4h; Reflux; Inert atmosphere; | 100% |
With sodium hydride In N,N-dimethyl-formamide at 20℃; for 14h; Etherification; | 87% |
With sodium hydroxide In ethanol | 82% |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 60℃; for 1.16667h; | 100% |
With potassium carbonate In N,N-dimethyl-formamide at 60℃; | 100% |
With potassium carbonate In acetonitrile for 3h; | 100% |
Conditions | Yield |
---|---|
In xylene for 0.00833333h; Heating; microwave irradiation; | 100% |
In toluene for 12h; Reflux; | 100% |
at 100℃; for 0.0333333h; Irradiation; | 99% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone Heating; | 100% |
With caesium carbonate In acetone at 20℃; | 100% |
With potassium carbonate In acetonitrile at 20℃; Reflux; | 98% |
Conditions | Yield |
---|---|
Stage #1: 2,4-Dihydroxybenzaldehyde With sodium hydrogencarbonate In acetonitrile at 20℃; for 0.75h; Inert atmosphere; Stage #2: benzyl bromide In acetonitrile Inert atmosphere; Reflux; | 100% |
With potassium hydrogencarbonate In acetonitrile for 15h; Reflux; | 85% |
With sodium hydrogencarbonate In acetonitrile for 15h; Reflux; | 85% |
Conditions | Yield |
---|---|
With TiCl2*2THF In tetrahydrofuran for 24h; Heating; | 100% |
With Wilkinson's catalyst; dimethyl zinc(II) In tetrahydrofuran; hexane at 20℃; for 1h; | 100% |
With hafnium(II) chloride In tetrahydrofuran for 12h; Heating; | 99% |
Conditions | Yield |
---|---|
With sodium iodide In acetone at 20℃; for 24h; | 100% |
With sodium iodide In acetone at 20℃; for 24h; Inert atmosphere; Darkness; | 100% |
With hydrogen iodide; cetyltributylphosphonium bromide at 60℃; for 0.0833333h; | 99% |
Conditions | Yield |
---|---|
In neat (no solvent) at 75℃; | 100% |
Inert atmosphere; Neat (no solvent); | 99% |
for 5h; Reflux; | 93% |
5-bromo-4-hydroxy-3-methoxybenzaldehyde
benzyl bromide
4-(benzyloxy)-3-bromo-5-methoxybenzaldehyde
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; Inert atmosphere; | 100% |
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 4h; | 97% |
With potassium carbonate In N,N-dimethyl-formamide at 50℃; | 94% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone Reflux; | 100% |
With potassium carbonate In acetone for 8h; Heating; | 97% |
With potassium carbonate In acetone for 8h; Heating / reflux; | 97% |
Conditions | Yield |
---|---|
Stage #1: isopropyl alcohol With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0℃; for 0.5h; Inert atmosphere; Stage #2: benzyl bromide In N,N-dimethyl-formamide; mineral oil at 0 - 20℃; for 5h; Inert atmosphere; | 100% |
With iron(II) sulfate at 75℃; for 12h; | 92% |
With silver(II) oxide Heating; | 90% |
With potassium hydroxide; tetrafluoroboric acid; mercury(II) oxide In dichloromethane 1.) room temp., 1 h; | 60% |
(i) Ag2O, (ii) Py, PhCOCl; Multistep reaction; |
Conditions | Yield |
---|---|
With potassium carbonate; tetrabutylammomium bromide for 96h; Ambient temperature; | 100% |
With 1,8-diazabicyclo[5.4.0]undec-7-ene In N,N-dimethyl-formamide at 80℃; for 2h; | 91% |
With 1-butyl-3-methylimidazolium hydroxide at 100℃; under 51.7148 Torr; for 0.0833333h; microwave irradiation; | 82% |
Conditions | Yield |
---|---|
With tetra-(n-butyl)ammonium iodide; sodium hydride In trichlorophosphate Heating; | 100% |
With tetra-(n-butyl)ammonium iodide; sodium hydride In tetrahydrofuran at 23℃; for 5.5h; | 100% |
With tetra-(n-butyl)ammonium iodide; sodium hydride In tetrahydrofuran; mineral oil at 0 - 23℃; for 18h; Inert atmosphere; Sealed tube; | 100% |
benzyl bromide
benzyl nitrate
Conditions | Yield |
---|---|
With silver nitrate In acetonitrile at 70℃; for 5h; Darkness; | 100% |
With silver nitrate In acetonitrile at 20℃; Nitration; | 97% |
With silver nitrate In acetonitrile at 20℃; for 24h; | 82% |
Conditions | Yield |
---|---|
Stage #1: 1H-imidazole With sodium hydride In N,N-dimethyl-formamide at 0 - 20℃; for 2h; Stage #2: benzyl bromide In N,N-dimethyl-formamide at 20℃; for 4h; | 100% |
Stage #1: 1H-imidazole With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0℃; for 0.25h; Stage #2: benzyl bromide In N,N-dimethyl-formamide; mineral oil at 25℃; for 3h; | 97% |
With caesium carbonate at 100℃; for 0.416667h; Microwave irradiation; | 90% |
Conditions | Yield |
---|---|
100% | |
In acetone Reflux; | 100% |
In toluene for 14h; Inert atmosphere; Reflux; | 72% |
Conditions | Yield |
---|---|
100% | |
In acetonitrile at 45℃; for 3h; | 99% |
In acetonitrile at 100℃; for 12h; | 98.71% |
Conditions | Yield |
---|---|
100% | |
at 0 - 20℃; | 99.6% |
at 0 - 20℃; | 99.6% |
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran for 4h; 0 deg C to 25 deg C; | 100% |
Stage #1: caprolactam With sodium hydride In tetrahydrofuran at 0℃; for 0.5h; Inert atmosphere; Stage #2: benzyl bromide In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 98% |
With sodium hydride In tetrahydrofuran; paraffin 1.) 0 deg C to room temperature, 2 h, 2.) room temperature, 2 h; | 96% |
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