hebei yanxi chemical co., LTD who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do research and developm
Cas:71-43-2
Min.Order:1 Metric Ton
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Type:Manufacturers
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
TIANFUCHEM--71-43-2--High purity Benzene factory price 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 rela
Cas:71-43-2
Min.Order:1 Metric Ton
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Type:Lab/Research institutions
inquiryEnglish Name: Benzene English synonyms: Benzene in dimethyl sulfoxide;Residual Solvent Class 1 - Benzene CAS: 71-43-2
Our company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At presen
Cas:71-43-2
Min.Order:1 Kilogram
FOB Price: $40.0 / 60.0
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
Hangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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:71-43-2
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquirySuperior quality, moderate price & quick delivery. Appearance:colourless liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum, or as per your request. Application:Used as Pharmaceutical Intermediat
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,
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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High purity, high success rate, short cycle and moderate priceAppearance:White powder solid Storage:Negative 20 degrees Celsius Package:5mg, 10mg 100mg, 1gram Application:Applied to various scientific research
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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
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:71-43-2
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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Benzene supplier in China CAS NO.71-43-2 Application:Benzene supplier in China CAS NO.71-43-2
1,we produce and sell good chemicals around the world. 2,our success rate is about 95%. this means, if customer order is accepted, the probability that the customer will obtain the ordered substances, is 95%. 3,our staff consists of highl
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Cas:71-43-2
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Min.Order:10 Milligram
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Type:Lab/Research institutions
inquiryBenzene Basic information Product Name: Benzene Synonyms: AKOS BBS-00004227;BENZENE;BENZENE 5000;BENZENE 300;BENZOL;CYCLOHEXATRIENE;PHENE;PHENYL HYDRIDE
Changzhou Xuanming Chemical Co., Ltd. is dedicated to the technology development, manufacturing, import and export chemicals, which are specialized in pharmaceutical intermediates, pesticide intermediate, industry of fine chemicals and custom synt
Product Description Product Name Benzene CAS 71-43-2 Function Pharmaceutical Intermediates
Cas:71-43-2
Min.Order:1 Metric Ton
FOB Price: $10.0
Type:Trading Company
inquiryConditions | Yield |
---|---|
With sodium hydroxide; ethanol; hydrogen; PdCl2-poly(N-vinyl-2-pyrrolidone); palladium dichloride at 65℃; under 760 Torr; for 2h; | 100% |
With 9-borabicyclo[3.3.1]nonane dimer; triphenylstannane In toluene at 0℃; | 100% |
With TiCpCl2; diisobutylaluminium hydride In 1,4-dioxane at 80℃; for 4h; Product distribution; further reagents(Zr, Hf complexes), solvents, and temperatures; further halobenzenes, alkyl, alkenyl and cyclopropyl halides; | 100% |
Conditions | Yield |
---|---|
With tetrabutoxytitanium; diisobutylaluminium hydride In diethyl ether for 6h; Heating; | 100% |
With sodium hydroxide; ethanol; PdCl2-poly(N-vinyl-2-pyrrolidone); palladium dichloride at 65℃; under 760 Torr; for 1h; | 100% |
With potassium tert-butylate; benzaldehyde In N,N-dimethyl-formamide at 90℃; for 1h; Schlenk technique; Inert atmosphere; | 99% |
cyclohexa-1,4-diene
benzene
Conditions | Yield |
---|---|
With [Mn(IV)(O)(BQCN)(H2O)](2+) In water; acetonitrile at 0℃; Kinetics; Concentration; Inert atmosphere; | 100% |
With Fe2(OH)0.6(2,5-dioxido-1,4-benzenedicarboxylate) at 24℃; | 100% |
With oxygen; 2,3-dicyano-5,6-dichloro-p-benzoquinone; sodium nitrite In toluene at 120℃; under 9750.98 Torr; for 8h; | 99% |
cyclohexa-1,3-diene
benzene
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide; polystyrene-bound phenylselenic acid In tetrachloromethane for 12h; Product distribution; Heating; var. aromatic species; var. reaction times; | 100% |
With iron(III) trifluoromethanesulfonate; C65H77N5O4S2 In 1,2-dichloro-ethane at 75℃; under 760.051 Torr; for 8h; Inert atmosphere; | 78% |
With [[HC-(CMeNC6H3(iPr)2)2]NiIII(O2)CuIII(N(indane)(2-pyridyl(ethylamine))2)](OTf) In dichloromethane at -60℃; Kinetics; Reagent/catalyst; Inert atmosphere; | 49% |
Conditions | Yield |
---|---|
With sodium hydroxide; ethanol; hydrogen; PdCl2-poly(N-vinyl-2-pyrrolidone); palladium dichloride at 65℃; under 760 Torr; for 2h; Product distribution; effect of bases and solvents on the hydrodechlorination; | 100% |
With potassium hydroxide; hydrogen; palladium on activated charcoal; Aliquat 336 In 2,2,4-trimethylpentane at 50℃; for 4.5h; | 100% |
With sodium hydroxide; ethanol; hydrogen; PdCl2-poly(N-vinyl-2-pyrrolidone); palladium dichloride at 65℃; under 760 Torr; for 2h; | 100% |
Conditions | Yield |
---|---|
With potassium hydroxide; hydrogen; palladium on activated charcoal; Aliquat 336 In water at 50℃; for 0.833333h; | 100% |
With di-tert-butyl peroxide; caesium carbonate; isopropyl alcohol at 120℃; for 3h; Inert atmosphere; | 93 %Chromat. |
With ammonium formate In methanol at 20℃; for 16h; |
5-cyclopentylidene-2,2-dimethyl-1,3-dioxane-4,6-dione
A
butatriene
B
ethene
C
carbon dioxide
D
cyclohexa-1,3-diene
E
acetone
F
benzene
Conditions | Yield |
---|---|
With variation of temp. at 550℃; Product distribution; | A 4% B 11.9% C 100% D 39.2% E 101.9 % F 3.3% |
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In water at 50℃; for 0.25h; | 100% |
With sodium hydroxide; ethanol; hydrogen; PdCl2-poly(N-vinyl-2-pyrrolidone); palladium dichloride at 65℃; under 760 Torr; for 6h; | 100% |
With Ni[1,10-phenanthroline]2(PF6)2; water; zinc at 70℃; for 7h; Ionic liquid; | 51.2% |
1,1-dicyano-2,2-bis(trifluoromethyl)ethene
A
2,2-Bis(trifluoromethyl)ethane-1,1-dicarbonitrile
B
benzene
Conditions | Yield |
---|---|
With cyclohexa-1,4-diene In chloroform-d1 Mechanism; Ambient temperature; or 1,3-cyclohexadiene, 2,5-dihydrofuran; | A 100% B 97% |
With cyclohexa-1,4-diene In chloroform-d1 Ambient temperature; also with 1,3-cyclohexadiene, 2,5-dihydrofuran; | A 100% B 97% |
C22H17ClN6O
A
4-Chloro-1-(4-methoxy-phenyl)-[1,2,4]triazolo[4,3-a]quinoxaline
B
benzene
Conditions | Yield |
---|---|
In chloroform-d1 at 60℃; for 0.0333333h; Product distribution; Thermodynamic data; Rate constant; other temperature, time; | A 100% B 80% |
5-(2-Chloro-phenoxy)-1-phenyl-1H-tetrazole
A
1-phenyl-5-hydroxytetrazole
B
benzene
Conditions | Yield |
---|---|
With cyclohexene; palladium on activated charcoal In ethanol; water; benzene for 4.16667h; Heating; | A n/a B 100% |
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal; Aliquat 336 In water at 50℃; for 0.25h; | 100% |
With cyclohexane; CeCl3/C; palladium dichloride at 300℃; Product distribution; Further Variations:; Reagents; Temperatures; | 99.9% |
With Ni[1,10-phenanthroline]2(PF6)2; water; zinc at 70℃; for 7h; Ionic liquid; | 58.2% |
Conditions | Yield |
---|---|
With sodium hydroxide; ethanol; hydrogen; PdCl2-poly(N-vinyl-2-pyrrolidone); palladium dichloride at 65℃; under 760 Torr; for 2h; | 100% |
With Ni[1,10-phenanthroline]2(PF6)2; water; zinc at 70℃; for 7h; Ionic liquid; | 46% |
With Ni-Al clusters In tetrahydrofuran for 1.5h; Dehalogenation; reduction; hydrogenolysis; dechlorination; Heating; |
Conditions | Yield |
---|---|
In (2)H8-toluene at 120℃; for 30h; | A 100% B n/a |
diphenyliodonium bromide
A
iodobenzene
B
biphenyl
D
bromo(phenyl)mercury
E
benzene
Conditions | Yield |
---|---|
In acetonitrile Kinetics; byproducts: C6H5Br; at different temp. between 20-70°C; UV; yields for 45°C; | A 100% B 6-7 C n/a D n/a E 1.4% |
diphenyliodonium chloride
A
iodobenzene
C
biphenyl
D
phenylmercury(II) chloride
E
benzene
Conditions | Yield |
---|---|
In acetonitrile Kinetics; at different temp. between 20-70°C; UV; yields for 45°C; | A 100% B 10-11 C 4-5 D 89-92 E 1.4% |
copper
A
fluorobenzene
B
iodobenzene
C
biphenyl
D
copper(I) tetrafluoroborate
E
benzene
Conditions | Yield |
---|---|
In acetonitrile Kinetics; stirred at 20-70°C; GLC; | A <1 B 100% C 95% D 99% E 5% |
Conditions | Yield |
---|---|
In chlorobenzene byproducts: benzene; stirring soln. under Ar for 48 h at 110°C; distn. of solvent, G.C.anal. of benzene; | A 100% B 100% |
(PPh3)3CoH(N2)
2,2,2-trifluoroethyl benzoate
A
(trifluoroethoxo)tris(triphenylphosphine)cobalt(I)
B
benzoic acid benzyl ester
C
nitrogen
D
hydrogen
E
benzene
Conditions | Yield |
---|---|
In toluene PhCOOCH2CF3 added to toluene soln. of CoH(N2)(PPh3)3, evacuated, stirred at 20°C for 2 days; | A n/a B 28% C 100% D 17% E 32% |
Conditions | Yield |
---|---|
With isopropyl alcohol at 150℃; under 7500.75 Torr; for 12h; Inert atmosphere; Autoclave; | A 25.1% B 100% C 74.9% |
With isopropyl alcohol at 160℃; for 15h; Autoclave; Inert atmosphere; | |
With isopropyl alcohol at 150℃; for 10h; Catalytic behavior; Reagent/catalyst; Temperature; Sealed tube; | A 24.6 %Chromat. B 47.8 %Chromat. C 24.3 %Chromat. |
With isopropyl alcohol at 150℃; for 6h; Temperature; Sealed tube; | A 15.2 %Chromat. B 17.7 %Chromat. C 5.8 %Chromat. |
phenyl(p-carboran-2-yl)iodonium tetrafluoroborate
A
iodobenzene
B
2-iodo-closo-1,12-dodecaborane
C
2-fluoro-p-caborane
D
benzene
Conditions | Yield |
---|---|
In dichloromethane; water 25°C, 0.6 h; | A 99% B 0% C 99.5% D <0.5 |
methane
benzene
Conditions | Yield |
---|---|
With hydrogen; molybdenum and barium-containing crystalline metallosilicate catalyst [Mo-B] at 200 - 700℃; Product distribution / selectivity; | 99% |
chromium(VI) oxide; HZHM (pentasil); platinum at 750℃; Product distribution; | 14% |
molybdenum for 2h; Product distribution / selectivity; Inert atmosphere; | 12.4% |
Conditions | Yield |
---|---|
at 930℃; under 0.1 Torr; Product distribution; Mechanism; detected by 13C nmr; | A 99% B 1% |
phenyl(p-carboran-2-yl)iodonium tetrafluoroborate
A
iodobenzene
B
2-iodo-closo-1,12-dodecaborane
C
2-fluoro-p-caborane
D
benzene
Conditions | Yield |
---|---|
In dichloromethane; water at 25°C, 0.5 h; | A 95% B <1 C 99% D <0.5 |
A
biphenyl
B
diphenyl sulfide
C
triphenylantimony
D
diphenyldisulfane
E
benzene
Conditions | Yield |
---|---|
In neat (no solvent) thermal decompn. of Sb compd. in a sealed tube on heating to 140°C for 3 h; not isolated, detected by GLC and TLC; | A 21% B 69% C 99% D 30% E 6% |
Conditions | Yield |
---|---|
With sodium hydroxide at 24.84℃; under 760.051 Torr; for 12h; Inert atmosphere; UV-irradiation; Sealed tube; | 99% |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In 1,2-dimethoxyethane at 35℃; for 4h; ultrasonic acceleration of reduction; | A 98% B n/a |
With lithium aluminium tetrahydride; Tridecane In diethyl ether at 0℃; for 0.25h; Irradiation; Title compound not separated from byproducts; | A 77 % Chromat. B 18 % Chromat. |
With Amberlite IRA-400; borohydride form; nickel diacetate In methanol at 20℃; for 3h; Reduction; | A 56 % Chromat. B 19 % Chromat. |
Conditions | Yield |
---|---|
With potassium hydroxide; PEG-6000 at 150℃; for 6h; | A 98% B n/a |
Conditions | Yield |
---|---|
With sodium methylate; bis-triphenylphosphine-palladium(II) chloride In dichloromethane at 40℃; under 11250.9 Torr; for 4h; | A 98% B 1% |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In 1,2-dimethoxyethane at 35℃; for 4h; ultrasonic acceleration of reduction; | A 98% B n/a |
Conditions | Yield |
---|---|
With aluminium trichloride for 19.5h; Heating; | 100% |
Friedel-Crafts reaction; | 90% |
iron(III) chloride at 109℃; for 0.458333h; Product distribution / selectivity; Irradiation; | 83% |
Conditions | Yield |
---|---|
With Nafion-H at 150℃; for 0.5h; Microwave irradiation; | 100% |
With boron trifluoride monohydrate at 50℃; for 2h; Sealed tube; | 98% |
With trifluorormethanesulfonic acid at 50℃; for 0.583333h; | 96% |
Conditions | Yield |
---|---|
With Anthyllis vulneraria/Noccaea caerulescens extracts supported in montmorillonite K10 at 25℃; for 3h; Friedel Crafts alkylation; regioselective reaction; | 100% |
lithium tetrakis(pentafluorophenyl)borate for 8h; Friedel-Crafts benzylation; Heating; | 96% |
With carbon monoxide at 130℃; under 7600.51 Torr; for 10h; Friedel-Crafts alkylation; | 95% |
Conditions | Yield |
---|---|
lithium tetrakis(pentafluorophenyl)borate for 8h; Friedel-Crafts benzylation; Heating; | 100% |
With phosphonic Acid at 150℃; for 36h; Inert atmosphere; | 56% |
aluminium trichloride In nitromethane at 20℃; Rate constant; | |
With aluminium trichloride |
Conditions | Yield |
---|---|
With zinc(II) chloride In dichloromethane at 20℃; for 24h; | 100% |
With aluminium trichloride | 58% |
With aluminum (III) chloride at 50 - 60℃; for 2h; | 50% |
Conditions | Yield |
---|---|
With aluminum (III) chloride In dichloromethane at 0 - 20℃; Friedel-Crafts Acylation; Inert atmosphere; | 100% |
With iron(III) oxide at 20℃; for 0.166667h; Friedel Crafts acylation; regioselective reaction; | 98% |
With zinc at 60 - 62℃; for 0.00833333h; Friedel-Crafts acylation; microwave irradiation; | 95% |
Conditions | Yield |
---|---|
With aluminum (III) chloride In dichloromethane at 0 - 20℃; Inert atmosphere; | 100% |
aluminium trichloride; nitromethane In carbon disulfide for 2h; Product distribution; Mechanism; Ambient temperature; further Friedel-Crafts catalysts, further arenes, further haloacid chlorides; variation of temperature and time; | 88% |
aluminium trichloride; nitromethane In carbon disulfide for 2h; Ambient temperature; | 88% |
Conditions | Yield |
---|---|
With aluminium trichloride In dichloromethane at 20 - 40℃; for 2.5h; | 100% |
With aluminum (III) chloride at 20 - 30℃; for 3h; Friedel-Crafts Acylation; | 90.1% |
With carbon disulfide; aluminium trichloride | |
With aluminium trichloride |
Conditions | Yield |
---|---|
With carbon dioxide; bromine at 40℃; under 187519 Torr; for 2h; Supercritical conditions; Green chemistry; | 100% |
With lead(II,IV) oxide; trifluoroacetic acid; potassium bromide at 20℃; Product distribution; reagents ratio; | 96% |
With gold(III) chloride; N-Bromosuccinimide In 1,2-dichloro-ethane at 80℃; for 24h; Inert atmosphere; regioselective reaction; | 94% |
Conditions | Yield |
---|---|
With cobalt(III) acetate; trifluoroacetic acid; potassium iodide In water at 25℃; for 0.00333333h; Mn(OAc)3 or (NH4)2Ce(SO4)3 instead Co(OAc)3; object of study: oxidative iodination promoted by Co(III), Ni(III) or Ce(IV); | 100% |
With cobalt(III) acetate; trifluoroacetic acid In water at 25℃; for 0.00333333h; | 100% |
With iodine; silver trifluoromethanesulfonate In dichloromethane at 20℃; | 100% |
Conditions | Yield |
---|---|
With hydrogen; [(norbornadiene)rhodium(I)chloride]2; polydiacetylene In n-heptane at 30℃; under 60800 Torr; for 0.9h; Product distribution; various aromatic compounds and other catalyst also investigated; | 100% |
With hydrogen; Ni-Tc on γ-Al2O3 at 175 - 250℃; under 760 Torr; Product distribution; dependence of catalytic activity on the reduction temperature; enhanced activity of bimetallic catalysts; | 100% |
With hydrogen; decacarbonyldirhenium(0) at 230℃; under 75005.9 Torr; for 0.25h; | 100% |
Conditions | Yield |
---|---|
With water-d2; [Ru(2,6-bis((di-t-Bu-phosphino)methyl)pyridine)(η2-H2)H2] In cyclohexane at 50℃; for 72h; | 100% |
With CD5(1+) In gas at 57.9℃; Rate constant; experiment conditions: NBS pulsed ion cyclotron resonance; | |
With C(2)H3CN(2)H(1+) In gas at 57.9℃; Rate constant; Mechanism; Thermodynamic data; experiment conditions: NBS pulsed ion cyclotron resonance; probability of a reactive H/D exchange encounter for the deuteronated ion as a function of the Gibbs free-energy change of the (endoergic) deuteron transfer reaction; further reagents; |
benzene
1,2,3,4,5,6-hexachlorocyclohexane
Conditions | Yield |
---|---|
With chlorine for 48h; Irradiation; | 100% |
With chlorine Rate constant; Irradiation; | |
With chlorine im Sonnenlicht; α-benzene hexachloride; |
Conditions | Yield |
---|---|
With tris-(2-chloro-ethyl)-amine; trifluorormethanesulfonic acid; trifluoroacetic acid In chloroform at 40℃; for 12h; Product distribution; Mechanism; various acids, various substrates; | 100% |
With trifluorormethanesulfonic acid; trimethylsilylazide at 55℃; for 0.833333h; Product distribution; Mechanism; other arenes or substituted arenes; var. temperatures and time; | 95% |
With trifluorormethanesulfonic acid; trimethylsilylazide In chloroform at 90℃; under 5250.53 Torr; for 0.0466667h; Flow reactor; | 86% |
Conditions | Yield |
---|---|
rhodium(II) trifluoroacetate dimer at 22℃; for 2h; Product distribution; other aromatic reaction partners, other diazo esters; | 100% |
rhodium(II) trifluoroacetate dimer at 22℃; for 2h; Product distribution; var. rhodium(II) salt; | 100% |
rhodium(II) trifluoroacetate dimer at 22℃; for 2h; | 100% |
Heating; |
diazoacetic acid ethyl ester
benzene
ethyl cyclohepta-2,4,6-trienecarboxylate
Conditions | Yield |
---|---|
With Ag3(μ2-(3,5-(CF3)2PyrPy))3 In dichloromethane; benzene at 25℃; for 2h; Catalytic behavior; Time; Solvent; Buchner Ring Enlargement; Darkness; | 100% |
rhodium(II) trifluoroacetate dimer at 22℃; for 2h; | 98% |
With C28H6Au2Cu2F24N2 In cyclohexane for 12h; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid at 20℃; for 3h; | 100% |
With aluminium trichloride at 60℃; for 2h; Yield given; |
Conditions | Yield |
---|---|
for 1h; Irradiation; | 100% |
In acetonitrile for 1h; Irradiation; | 98% |
at 20℃; Quantum yield; Irradiation; | |
With benzophenone at 20℃; Quantum yield; Further Variations:; Reagents; Irradiation; |
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