Items Standard Result Appearance Colorless liquid Complies Assay 99.8%min 99.99
Cas:75-09-2
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Cas:75-09-2
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inquiryChemical name:Dichloromethane Molecular formula: CH2Cl2 Structural formula: Molecular weight: 84.93 CAS No.: 75-09-2 Physicochemical property: With pungent smell similar to ether; vapor pressure: 30.55kPa(10℃); melting point: -95.1℃; solubili
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
Cas:75-09-2
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inquiryTIANFUCHEM-- 75-09-2--High purity Dichloromethane 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
Cas:75-09-2
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inquiryProduct Description Product website: http://www.finerchem.com Product Name Dichloromethane CAS No. 75-09-2
Cas:75-09-2
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inquiryProduct Name Methylene chloride / MC Appearance Colorless, volatile liquid with a moderately sweet aroma is widely used as a solvent CAS NO.
Cas:75-09-2
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inquiryOur 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 present
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inquiryAdvantage : LIDE PHARMACEUTICALS LTD. is a mid-small manufacturing-type enterprise, engaged in pharmaceutical intermediates of R&D, custom-made and production, and also involving trading chemicals for export. We have established the R&
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inquiryCompany information: Hebei Mojin Biotechnology Co., Ltd, Our company is a professional in carbomer,carbopol,lead acetate,meglumine diphenyl ethylamine and other chemical raw materials and chemical reagents research and development production ente
Cas:75-09-2
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inquiryProduct Name: Dichloromethane Synonyms: Dichloromethane, Guaranteed Reagent Grade;Aerothene MM;CH2Cl2;Chlorure de methylene;chloruredemethylene;chloruredemethylene(french);Dichlormethan;dichloro-methan CAS: 75-09-2 MF: CH2Cl2 MW: 84.93 EI
Cas:75-09-2
Min.Order:1 Kilogram
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inquiryOur Services 1. New Molecules R&D 2. Own test center HPLC NMR GC LC-MS 3. API and Intermediates from China reputed manufacturers 4. Documents support COA MOA MSDS DMF open part Our advantages 1. Government awarded company. Top 100 enter
Cas:75-09-2
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inquiryA substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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
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:75-09-2
Min.Order:10 Gram
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inquiryProduct 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:75-09-2
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Cas:75-09-2
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inquiryProduct name: Dichloromethane CAS No.: 75-09-2 Molecule Formula:CH2Cl2 Molecule Weight:84.93 Purity: 99.0% Package: 200kg/drum Description: Colorless transparent liquid Manufacture Standards:Enterprise Standard TES
Cas:75-09-2
Min.Order:1 Kilogram
Negotiable
Type:Trading Company
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
Hangzhou Fanda Chemical Co.,Ltd (FandaChem) , a China-based chemical company, specialize in exporting Dichloromethane CAS:75-09-2;Please contact us by email freely. We are leading exporter in China. If you really need this c
Cas:75-09-2
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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
best quality best price best service Appearance:Clear and colorless liquid Package:ISO TANK CONTAINER Application:DCM is a widely used solvent Also is the raw material for the production of fungicides, nitrile bacterazole and imidazole Used
Cas:75-09-2
Min.Order:0 Metric Ton
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Type:Trading Company
inquirySuperior quality, moderate price & quick delivery. Appearance:colorless liquid Storage:Keep containers tightly closed. Keep in original container. Keep away from heat Package:250 kg net weight/ 200L export standard drum Application:serves for c
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
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Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:75-09-2
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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Conditions | Yield |
---|---|
With chloroform In toluene under Ar; stirred at 20°C for 5 h; stored overnight at 0-5°C; evaporated, extracted (THF); elem. anal.; | A 57% B 88% |
1,2-Dichloroethylene
A
dichloromethane
B
1,2-bis(trichlorosilyl)ethane
C
1,2-bis(trichlorosilyl)ethene
D
1,1,1,3,3,3-hexachloro-1,3-disilapropane
Conditions | Yield |
---|---|
With hexachlorodisilane at 550℃; for 0.00833333h; | A n/a B n/a C 83% D n/a |
Conditions | Yield |
---|---|
With KOH In water; butan-1-ol heating of (CH3)2(CHCl2)SiOSi(CH3)2(CHCl2) and 10% KOH in n-butanol/H2O at 45°C under reduced pressure;; | 78% |
With KOH In potassium hydroxide aq. KOH; (CH3)2(CHCl2)SiOSi(CH3)2(CHCl2) and 40% aq. KOH;; | |
With potassium hydroxide In potassium hydroxide (CH3)2(CHCl2)SiOSi(CH3)2(CHCl2) and 40% aq. KOH;; |
Conditions | Yield |
---|---|
With chloroform In toluene under Ar; excess of CHCl3 added to suspension of Cp3ZrH in PhMe; stirred at about 20°C for 5 h; stored overnight at 0-5°C; evaporated, extracted (THF), filtered; filtrate evapd.; elem. anal.; | A 70% B 42% |
Conditions | Yield |
---|---|
With sulfur dioxide; chlorine at 25℃; under 2250.23 Torr; for 1h; Concentration; Wavelength; Irradiation; | A n/a B 69% |
Conditions | Yield |
---|---|
With chloroform In toluene under Ar; elem. anal.; | A 67% B 43% |
methane
A
tetrachloromethane
B
methylene chloride
C
dichloromethane
D
chloroform
E
methanesulfonyl chloride
Conditions | Yield |
---|---|
With hydrogenchloride; sulfur dioxide; chlorine at 63 - 67℃; under 6750.68 Torr; Photolysis; | A n/a B n/a C n/a D n/a E 55% |
methane
A
dichloromethane
B
chloroform
C
methanesulfonyl chloride
Conditions | Yield |
---|---|
With sulfur dioxide; chlorine at 65℃; under 2250.23 Torr; for 1h; Temperature; Irradiation; | A n/a B n/a C 54.9% |
Conditions | Yield |
---|---|
With tetra-n-butylphosphonium formate In water at -20 - 22℃; for 1.33333h; Reagent/catalyst; | A 26% B 52% |
With [RuCl(1-butyl-3-methyl-imidazole)(1,3,5-triaza-7-phosphatricyclo[3.3.1.1]3,7decane)(η6-p-cymene)]Cl; hydrogen; sodium formate In water at 80℃; under 7500.75 Torr; for 2h; Schlenk technique; Sealed tube; | A 12.9% B 29% |
With isopropyl alcohol; dimanganese decacarbonyl at 120℃; Product distribution; catalyst and temperature effects; |
Conditions | Yield |
---|---|
With iodine trichloride Product distribution; further iodoalkanes; | A 34% B 50% |
Dichlorofluoromethane
benzene-d6
Triethylgerman
A
R32
B
dichloromethane
C
bis-pentadeuteriophenyl-methane
D
triethylchlorogermane
Conditions | Yield |
---|---|
With ACF. Et3GeH In benzene-d6 at 70℃; for 216h; Schlenk technique; Inert atmosphere; | A 50% B 11% C 39% D n/a |
chloro-trimethyl-silane
chloroform
A
dichloromethane
B
trichloromethyltrimethylsilane
Conditions | Yield |
---|---|
With hexaethylphosphoric triamide In acetonitrile at 20℃; for 144h; | A n/a B 47% |
chloroform
A
dichloromethane
B
(dichlorosilylmethyl)trichlorosilane
C
1,1,1,3,3,3-hexachloro-1,3-disilapropane
Conditions | Yield |
---|---|
With trichlorosilane at 100℃; for 8h; | A 42% B 5% C 42% |
Chlorodifluoromethane
Triethylgerman
A
methylene chloride
B
dichloromethane
C
trifluoromethan
D
triethylchlorogermane
Conditions | Yield |
---|---|
With ACF. Et3GeH at 25℃; for 72h; Schlenk technique; Inert atmosphere; | A 41% B 32% C 27% D n/a |
chloroform
aniline
A
dichloromethane
B
phenyl isocyanate
C
Azobenzene
D
N-phenylphenylene-1,4-diamine
E
N-phenyl-1,2-benzenediamine
F
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
at 15℃; for 24h; Product distribution; Mechanism; Irradiation; | A n/a B 30.2% C 12.5% D 10.5% E 18.4% F n/a |
chloroform
Triethylgerman
A
methylene chloride
B
dichloromethane
C
triethylchlorogermane
Conditions | Yield |
---|---|
With ACF. Et3GeH at 70℃; Schlenk technique; Glovebox; | A 22% B n/a C n/a |
Dichlorofluoromethane
Triethylgerman
A
Difluoromethane
B
dichloromethane
C
trifluoromethan
D
Chlorodifluoromethane
E
triethylchlorogermane
Conditions | Yield |
---|---|
With ACF. Et3GeH at 25℃; for 72h; Schlenk technique; Inert atmosphere; | A n/a B n/a C 22% D 16% E n/a |
methylenesulfurtetrafluoride
A
dichloromethane
B
Methylschwefelpentafluorid
C
cis-Methylschwefelchloridtetrafluorid
D
cis-(Chlormethyl)schwefelchloridtetrafluorid
Conditions | Yield |
---|---|
With chlorine In trichlorofluoromethane at -78℃; | A n/a B n/a C n/a D 20% E n/a |
chloroform
benzene-d6
Triethylgerman
A
dichloromethane
B
bis-pentadeuteriophenyl-methane
C
triethylchlorogermane
Conditions | Yield |
---|---|
With ACF. Et3GeH at 70℃; Schlenk technique; Glovebox; | A n/a B 18% C n/a |
methane
A
tetrachloromethane
B
methylene chloride
C
dichloromethane
D
chloroform
Conditions | Yield |
---|---|
With chlorine for 4h; Product distribution; Ambient temperature; var. catalysts and times; | A 4.8% B 6.5% C 15% D 14% |
With molybdenum(V) chloride at 699.9℃; Product distribution; Mechanism; var. time, temp., and transition-metal chlorides; var. methane and argon flow rates; | |
With copper dichloride In melt at 449.9℃; Kinetics; Product distribution; further temperatures and concentrations; |
tetrachloromethane
Triethylgerman
A
dichloromethane
B
chloroform
C
triethylchlorogermane
Conditions | Yield |
---|---|
With ACF. Et3GeH at 70℃; Schlenk technique; Glovebox; | A 8% B n/a C n/a |
tetrachloromethane
benzene-d6
Triethylgerman
A
dichloromethane
B
chloroform
C
bis-pentadeuteriophenyl-methane
D
triethylchlorogermane
Conditions | Yield |
---|---|
With ACF. Et3GeH at 70℃; Schlenk technique; Glovebox; | A 7% B n/a C 6% D n/a |
pentacarbonyl(methoxyphenylmethylene)tungsten(0)
A
1,1,2,2-tetrachloroethylene
B
methylene chloride
C
dichloromethane
D
chloroform
Conditions | Yield |
---|---|
In tetrachloromethane byproducts: HCl, Cl2; further products; N2; stirred; gas-chromy., MAS; elem. anal.; | A 6.8% B 2% C 0.2% D 3.6% |
Conditions | Yield |
---|---|
With isopropyl alcohol In acetonitrile at 20℃; Reagent/catalyst; | |
With sodium hydroxide; iron(II) sulfate |
Conditions | Yield |
---|---|
With potassium hydroxide; tetrabutylammomium bromide for 13h; Ambient temperature; | 100% |
With sodium hydroxide; phase transfer catalysis by tetraethylammonium bromide for 16h; Ambient temperature; | 96% |
With tetrabutylammomium bromide; sodium hydroxide Inert atmosphere; Reflux; | 87% |
acetophenone oxime
dichloromethane
1-Phenyl-ethanone O-[1-phenyl-eth-(E)-ylideneaminooxymethyl]-oxime
Conditions | Yield |
---|---|
With 18-crown-6 ether; potassium carbonate | 100% |
With 1-butyl-3-methylimidazolium Tetrafluoroborate; sodium hydroxide at 20℃; for 0.5h; | 96% |
With sodium hydroxide In water for 17.5h; | 95% |
With sodium hydroxide; trialkyl-methyl-ammonium chloride |
3-benzoylpyrrole
dichloromethane
[1-(2-Benzoyl-pyrrol-1-ylmethyl)-1H-pyrrol-2-yl]-phenyl-methanone
Conditions | Yield |
---|---|
With sodium hydroxide; tetra-(n-butyl)ammonium iodide In dichloromethane for 4h; | 100% |
Conditions | Yield |
---|---|
With potassium hydroxide; benzyltrimethylammonium chloride In water at 40℃; for 72h; | 100% |
With potassium hydroxide; benzyltrimethylammonium chloride In dichloromethane at 40℃; for 72h; | 100% |
Stage #1: 4-chloro-phenol With sodium hydride In 1-methyl-pyrrolidin-2-one Stage #2: dichloromethane In 1-methyl-pyrrolidin-2-one at 40℃; for 9h; | 98% |
With 1-methyl-pyrrolidin-2-one; sodium hydride at 40℃; for 9h; | 98% |
With sodium hydroxide; Amberlite IRA-400 (Cl-) 2.) reflux, 15 h; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
With potassium hydroxide; octopus-type calixarene at 40℃; for 24h; Product distribution; also with substituted phenols; effect of catalysts poly(ethylene glycol)diethyl ether, poly(ethylene glycol), benzyltrimethylammonium chloride, none; also with water solvent; | 100% |
With potassium hydroxide; octopus-type calixarene at 40℃; for 24h; | 100% |
With potassium hydroxide; 5,11,17,23,29,35-Hexa-p-tert-butyl-37,38,39,40,41,42-hexakis-(3,6,9-trioxadecyloxy)calix<6>arene In dichloromethane at 40℃; for 24h; | 100% |
dichloromethane
(2R,3R)-3-(methylamino)-3-phenyl-1,2-propanediol
Conditions | Yield |
---|---|
at 100℃; for 28h; Cyclization; | 100% |
Conditions | Yield |
---|---|
at 55℃; | 100% |
dichloromethane
diethylamine
2,2-dimethyl-2H-1-benzopyran-6-sulfonyl chloride
N,N-diethyl-2,2-dimethyl-2H-1-benzopyran-6-sulfonamide
Conditions | Yield |
---|---|
In water | 100% |
dichloromethane
1-(bromomethyl)-4-methyl-2-(phenylmethoxy)benzene
<4-methyl-2-(phenylmethoxy)phenyl>acetonitrile
Conditions | Yield |
---|---|
With NaCN; tetrabutylammomium bromide In water | 100% |
dichloromethane
2-fluorobenzonitrile
(2S)-2-amino-5-(2-cyanophenylamino)pentanoic acid
Conditions | Yield |
---|---|
With hydrogenchloride; sodium hydroxide; acetic acid In ethanol; water | 100% |
dichloromethane
5-Chlorovaleroyl chloride
1,4-dihydro-4-(3-aminophenyl)-2,6-dimethyl-3,5-pyridinedicarboxylic acid,dimethyl ester
Conditions | Yield |
---|---|
In tetrahydrofuran; water; ethyl acetate | 100% |
In tetrahydrofuran; water; ethyl acetate | 100% |
In tetrahydrofuran; water; ethyl acetate | 100% |
dichloromethane
2-bromo-5-methoxy-1-(phenylmethyl)-1H-indole-3-acetic acid phenylmethyl ester
2-bromo-5-methoxy-1-(phenylmethyl)-1H-indole-3-acetamide
Conditions | Yield |
---|---|
With hydrogenchloride; aluminium In benzene | 100% |
2-carboxy-4-chloroquinoline
dichloromethane
water
Methyl-4-chloroquinaldate
Conditions | Yield |
---|---|
With NaH In N,N-dimethyl-formamide | 100% |
dichloromethane
tert-butylamine
3,4-diethoxy-3-cyclobuten-1,2-dione
3-(1,1-dimethylethylamino)-4-ethoxy-3-cyclobutene-1,2-dione
Conditions | Yield |
---|---|
In tetrahydrofuran; methanol | 100% |
dichloromethane
di-tert-butyl dicarbonate
Conditions | Yield |
---|---|
100% |
5-METHOXY-2-((3,5-DIMETHYL-4-NITRO-2-PYRIDINYL-N-OXIDE)-METHYLTHIO)-1H-BENZIMIDAZOLE
dichloromethane
5-methoxy-2-[[(4-methoxy-3,5-dimethylpyridin-2-yl-1-oxide)methyl]sulfanyl]-1H-benzimidazole
Conditions | Yield |
---|---|
With N-benzyl-N,N,N-triethylammonium chloride; sodium methylate In methanol; water | 100% |
diazomethane
methyl α-tert-butoxycarbonylamino-p-carboxymethylphenylacetate
dichloromethane
Methyl α-tert-butoxycarbonylamino-p-methoxycarbonylmethylphenylacetate
Conditions | Yield |
---|---|
100% |
Conditions | Yield |
---|---|
In ethanol (under Ar, Schlenk); Rh-complex added to refluxing soln. of Sb(C6H5)3 inEtOH; ppt. filtered, washed with CH2Cl2/hexane, dried in vacuo; elem. anal.; | 100% |
Conditions | Yield |
---|---|
In acetone byproducts: AgCl; soln. of palladium complex treated with AgClO4 in absence of light; 30 min stirred at room temp.; added to soln. of p-nitroaniline; soln. stirred at room temp. for 30 min; solvent evapd.; oil treated with Et2O; solid pptd.; elem. anal.; | 100% |
dichloromethane
Conditions | Yield |
---|---|
In dichloromethane soln. of Pt complex in CH2Cl2 stored at room temp. for 10 d; solvent evapd.; washed with hexane; elem. anal.; | 100% |
Conditions | Yield |
---|---|
In not given Atherton, M. J.; Fawcett, J.; Holloway, J. H.; Hope, E. G.; Karacar, A.;Russell, D. R.; Saunders, G. C. J. Chem. Soc., Dalton Trans. 1996, 321 5; elem. anal.; | 100% |
dichloro( 1,5-cyclooctadiene)platinum(ll)
dichloromethane
(bromodifluoromethyl)diphenylphosphine
Conditions | Yield |
---|---|
In dichloromethane by a react. of Ph2PCF2Br with Pt-contg. compd. at 20°C for 0.2 h; elem. anal.; | 100% |
tetrakis(actonitrile)copper(I) hexafluorophosphate
dichloromethane
n-butyl isonitrile
3,5-bis[bis-(4,5-diphenyl-1-methylimidazol-2-yl)methoxymethyl]pyrazole
Conditions | Yield |
---|---|
With KOC(CH3)3 In tetrahydrofuran; acetonitrile (N2, glove box) a soln. of Cu-complex in CH3CN was added to a soln. of pyrazole-compound and KOC(CH3)3 in THF, stirred for 15 min, n-butylisocyanide was added, stirred for 20 min; the solvent was removed in vac., the solid was dissolved in CH2Cl2 and filtered; elem. anal.; | 100% |
trichlorotris(tetrahydrofuran)chromium(III)
dichloromethane
2,6-bis(1-methylimidazol-2-ylidene)pyridine
Conditions | Yield |
---|---|
In tetrahydrofuran (N2); std. Schlenk technique; soln. of carbene in THF was slowly added to soln. of Cr complex in THF; stirred for 1 h; filtered; washed (THF, CH2Cl2); dried (vac.); elem. anal.; | 100% |
Conditions | Yield |
---|---|
at 25℃; Kinetics; | 100% |
Conditions | Yield |
---|---|
In dichloromethane (N2, Schlenk) a soln. of complex in CH2Cl2 allowed to stand for 2 h; volatiles were removed under vac.; elem. anal.; | 100% |
[ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2
dichloromethane
Conditions | Yield |
---|---|
In dichloromethane (under N2, Schlenk); soln. of Ru-complex in CH2Cl2 added dropwise to soln. of ligand in CH2Cl2, stirred for 1 h; concd., hexane added; elem. anal.; | 100% |
Conditions | Yield |
---|---|
In chloroform at 60℃; under 14251400 Torr; for 24h; Kinetics; Pressure; Temperature; Menshutkin Reaction; High pressure; Autoclave; | 100% |
for 0.25h; Microwave irradiation; Reflux; | 48% |
at 75℃; for 24h; | 42.6% |
Conditions | Yield |
---|---|
With [D]-sodium hydroxide; sodium acetate In water-d2 for 2h; pD >11; | 100% |
Conditions | Yield |
---|---|
In acetonitrile inert atmosphere, Schlenk technique; soln. of Pd-complex in CH3CN treated at -40 °C with (H3C)3OBF4, stirred at -40 °C for 60 min,warmed to room temp., solvent removed (vac.), recrystd. from petroleum ether/CH2Cl2; elem. anal.; | 100% |
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