good factory price and good quality methanol is an important organic solvent with better solubility than ethanol and can be used to modulate paint. Some inorganic salts such as sodium iodide, calcium chloride, ammonium nitrate, copper sulfate
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Cas:67-56-1
Min.Order:1 Metric Ton
Negotiable
Type:Manufacturers
inquiryHebei yanxi chemical co. LTD. has expanded a compositive entity from initially only as a small manufacturer. The company dedicated to the development, production and marketing of chemicals. After many years of efforts, we have established stable
high 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
Methyl alcohol Alias:Methyl alcohol Appearance and property:colorless and clear liquid,A pungent odor. Slight alcohol-like odor, volatile, mobile, smokeless blue flame combustion, with water, alcohols, ethers and o
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 advantage:Our company was built in 2009 with an ISO certificate.In the past 5 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 Scientif
Cas:67-56-1
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryProduct name Methanol MF CH3OH Color Colorless liquid Purity 99.7% Application Industrial grade Appearance: Colorless Tra
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Cas:67-56-1
Min.Order:100 Kilogram
Negotiable
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
Appearance:Colorless liquid Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:from MeSH Methanol is used as a ... Transportation:Common products:Sea/Air/Courier Dan
Cas:67-56-1
Min.Order:100 Metric Ton
Negotiable
Type:Lab/Research institutions
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:67-56-1
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryHangzhou 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
A 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:67-56-1
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquiryMethanolAppearance:Colorless liquid Storage:Keep away of light, cool place Package:according to customers' requirements Application:Pharmaceutical intermediates Transportation:By air(EMS or EUB or FedEx or TNT ect...) or by sea(FOB or CIF or CNF ect.
Superior quality, moderate price & quick delivery. Appearance:COLOURLESS LIQUID Storage:Well-sealed and put in dry and cool conditions. Protected from direct sunlight or high temperature. Package:as per your request Application:Suitable f
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:67-56-1
Min.Order:1 Metric Ton
Negotiable
Type:Lab/Research institutions
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
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Cas:67-56-1
Min.Order:100 Gram
Negotiable
Type:Lab/Research institutions
inquiryhigh purity, manufacturer Application:Intermediate
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:67-56-1
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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Methanol CAS. NO. 67-56-1 Application:Methanol CAS. NO. 67-56-1
Conditions | Yield |
---|---|
With water In aq. phosphate buffer at 20℃; for 1h; pH=7.4; Catalytic behavior; Reagent/catalyst; Electrolysis; Inert atmosphere; Enzymatic reaction; | 100% |
With cobalt(III) acetylacetonate; hydrogen; bis(trifluoromethanesulfonyl)amide; [2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine] In tetrahydrofuran; ethanol at 100℃; under 52505.3 Torr; for 24h; Autoclave; Inert atmosphere; | 59% |
With C36H54IrN2P2(1+)*C24H20B(1-); hydrogen; sodium hydride In ethanol; toluene at 180℃; under 7500.75 - 45004.5 Torr; for 18h; Autoclave; | 31% |
benzoic acid methyl ester
2-Ethylhexyl alcohol
A
methanol
B
Velate 368
Conditions | Yield |
---|---|
With phosphorus pentoxide; potassium carbonate; Aliquat 336 In neat (no solvent) under 20 Torr; for 8h; Product distribution; Ambient temperature; | A n/a B 100% |
With phosphorus pentoxide; potassium carbonate; Aliquat 336 In neat (no solvent) under 20 Torr; for 8h; Ambient temperature; | A n/a B 100% |
1,4-benzenedicarboxylic acid dimethyl ester
2-Ethylhexyl alcohol
A
methanol
B
2-ethylhexyl methyl terephthalate
Conditions | Yield |
---|---|
With phosphorus pentoxide; potassium carbonate; Aliquat 336 In neat (no solvent) under 20 Torr; for 24h; Product distribution; Ambient temperature; | A n/a B 100% |
With phosphorus pentoxide; potassium carbonate; Aliquat 336 In neat (no solvent) under 20 Torr; for 24h; Ambient temperature; | A n/a B 100% |
Conditions | Yield |
---|---|
With D-glucose; NADH In aq. buffer for 2h; pH=6.85; Catalytic behavior; Solvent; Concentration; pH-value; Ionic liquid; Enzymatic reaction; | 100% |
With carbon monoxide; water; hydrogen at 35 - 250℃; under 825.083 - 75007.5 Torr; Temperature; Pressure; Large scale; | 99.99% |
With dimethylsulfide borane complex; C24H18BO2P In benzene-d6 at 70℃; under 1520.1 Torr; for 1h; Reagent/catalyst; Inert atmosphere; | 95% |
dimethyl(p-nitrophenyl)sulfonium perchlorate
A
methanol
B
1-methylthio-4-nitro-benzene
Conditions | Yield |
---|---|
With water at 80℃; Rate constant; other temp.; | A n/a B 100% |
Conditions | Yield |
---|---|
With Methyltrichlorosilane; sodium iodide In acetonitrile at 25℃; for 6h; | A n/a B 100% |
1-(2-Adamantylidene)-1-methoxy-1-phenylmethane
A
methanol
B
adamantan-2-yl(phenyl)methanone
Conditions | Yield |
---|---|
With tris-p-bromophenyl ammoniumyl hexachloroantimonate In dichloromethane for 3h; | A n/a B 100% |
A
methanol
Conditions | Yield |
---|---|
With trifluoroacetic acid In benzene for 0.5h; pinacol rearrangement; | A n/a B 100% |
Conditions | Yield |
---|---|
With trifluoroacetic acid In benzene at 25℃; for 0.5h; pinacol rearrangement; | A n/a B 100% |
benzoic acid methyl ester
3-Phenylpropenol
A
methanol
B
cinnamyl benzoate
Conditions | Yield |
---|---|
2[{Cl(C6F13CH2CH2)2SnOSn(CH2CH2C6F13)2Cl}2] In various solvent(s) at 150℃; for 16h; | A n/a B 100% |
ethanol
3-phenylpropanoic acid methyl ester
A
methanol
B
ethyl dihydrocinnamate
Conditions | Yield |
---|---|
2[{Cl(C6F13CH2CH2)2SnOSn(CH2CH2C6F13)2Cl}2] In various solvent(s) at 150℃; for 16h; | A n/a B 100% |
3-Phenylpropenol
3-phenylpropanoic acid methyl ester
A
methanol
B
3-phenyl-2-propenyl benzenepropanoate
Conditions | Yield |
---|---|
2[{Cl(C6F13CH2CH2)2SnOSn(CH2CH2C6F13)2Cl}2] In various solvent(s) at 150℃; for 16h; | A n/a B 100% |
3-phenylpropanoic acid methyl ester
8-(tert-butyldimethylsiloxy)octan-1-ol
A
methanol
Conditions | Yield |
---|---|
2[{Cl(C6F13CH2CH2)2SnOSn(CH2CH2C6F13)2Cl}2] In various solvent(s) at 150℃; for 16h; | A n/a B 100% |
Conditions | Yield |
---|---|
With zeolite beads at 120 - 385℃; Product distribution / selectivity; | 100% |
A
methanol
Conditions | Yield |
---|---|
tetrabutyl ammonium fluoride In n-heptane at 100 - 114℃; Conversion of starting material; | A 100% B 100% |
tetrabutoxytitanium In n-heptane at 100 - 120℃; Conversion of starting material; | A 100% B 100% |
lithium hydroxide In n-heptane at 100 - 120℃; Conversion of starting material; | A 100% B 100% |
lithium stearate In n-heptane at 100 - 120℃; Conversion of starting material; | A 100% B 100% |
2-benzoyloxyacetaldehyde dimethyl acetal
2-hydroxyethanethiol
A
methanol
B
2-[(phenylcarbonyloxy)methyl]-1,3-oxathiolane
Conditions | Yield |
---|---|
toluene-4-sulfonic acid In toluene Heating; | A n/a B 100% |
tris(methyloxycarbonylmethyl)methane
4-methoxy-benzylamine
A
methanol
B
tris(methyloxycarbonylmethyl)methane
Conditions | Yield |
---|---|
at 120℃; for 24h; | A n/a B 100% |
2,6-di-tert-butyl-4-methylpyridine
methyltriphenylbismuthonium tetrafluoroborate
A
methanol
B
Dimethyl ether
C
2,6-di-tert-butyl-4-methylpyridinium tetrafluoroborate
D
triphenylbismuthane
Conditions | Yield |
---|---|
With H2O In chloroform-d1 water was added to mixt. (Ph3BiMe)(BF4) and 2,6-di-tert-butyl-4-methylpyridine in CDCl3 and mixt. was allowed to stand at room temp. for 33 h; detn. by NMR; | A 30% B 16% C 100% D 100% |
sodium tetramethoxyborate
methanol
Conditions | Yield |
---|---|
With Glauber's salt for 0.166667h; Ball milling; neat (no solvent); | 100% |
Conditions | Yield |
---|---|
With hydrogen; 10%Ru/C In water at 100℃; under 15001.5 Torr; for 2h; Product distribution / selectivity; Autoclave; | 100% |
With magnesium oxide In water at 250℃; for 3h; Inert atmosphere; | |
With magnesium oxide In water for 3h; Reagent/catalyst; Inert atmosphere; | |
With Ag/CaO-SiO2 Reagent/catalyst; Inert atmosphere; |
1,3-bis(4-hydroxybutyl)tetramethyldisiloxane
dimethoxy(methyl)phenylsilane
A
methanol
Conditions | Yield |
---|---|
With hydrogenchloride In water for 4.5h; Heating / reflux; | A n/a B 100% |
Conditions | Yield |
---|---|
With 1,1′-(pyridine-2,6-diylbis(methylene))bis(3-butylimidazolium) dibromide; carbonylchlorohydridobis(tricyclohexylphosphine)ruthenium(II); potassium tert-butylate; hydrogen In 1,4-dioxane at 130℃; under 37503.8 Torr; for 12h; Catalytic behavior; Reagent/catalyst; Temperature; Pressure; Autoclave; | A 39% B 100% |
With hydrogen In 1,4-dioxane at 250℃; under 30003 Torr; for 4h; Temperature; Solvent; Reagent/catalyst; Flow reactor; | A 93% B 99% |
With C24H38Cl2N3PRu; hydrogen; sodium methylate In tetrahydrofuran at 25℃; under 38002.6 Torr; for 16h; Autoclave; | A 99 %Chromat. B 95% |
N,N-dimethyl-formamide
methanol
Conditions | Yield |
---|---|
With potassium phosphate; carbonylhydrido(tetrahydroborato)[bis(2-diphenylphosphinoethyl)amino]ruthenium(II); hydrogen In tetrahydrofuran at 155℃; under 37503.8 Torr; for 18h; Catalytic behavior; Inert atmosphere; Sealed tube; | 100% |
With potassium phosphate; C29H55FeNOP2; hydrogen In tetrahydrofuran at 130℃; under 37503.8 Torr; for 3h; Catalytic behavior; Temperature; Pressure; | > 99 %Spectr. |
With C24H38Cl2N3PRu; potassium tert-butylate; hydrogen In isopropyl alcohol at 110℃; under 30402 Torr; for 30h; Temperature; Autoclave; Glovebox; |
9-methoxy-9-BBN
methanol
Conditions | Yield |
---|---|
With water at 20℃; for 0.5h; | 100% |
With water In tetrahydrofuran at 20℃; for 1h; | 96% |
Methyl formate
dimethyl amine
A
methanol
B
N,N-dimethyl-formamide
Conditions | Yield |
---|---|
under 2327.23 Torr; Industry scale; | A n/a B 99.97% |
methane
dinitrogen monoxide
A
methanol
B
formaldehyd
C
carbon dioxide
D
carbon monoxide
E
nitrogen
Conditions | Yield |
---|---|
In neat (no solvent) Kinetics; Oxidation of CH4 by N2O in presence of catalyst (773 K): deposited Cu(2+) on carbon;; | A 0.2% B 0.3% C 99.5% D 0% E n/a |
In neat (no solvent) Kinetics; byproducts: C2H5OH (small quantity); oxidation of CH4 by N2O in presence of catalyst (773 K): deposited Ti(4+) on carbon;; | A 13.8% B 0% C 86.2% D 0% E n/a |
In neat (no solvent) Kinetics; Oxidation of CH4 by N2O in presence of catalyst (773 K): deposited Co(2+) on carbon;; | A 0% B 0% C 75% D 25% E n/a |
Conditions | Yield |
---|---|
With C21H37N2OPRu; hydrogen In 1,4-dioxane at 145℃; under 6840.46 Torr; for 36h; | 99% |
dodecacarbonyl-triangulo-triruthenium; P(C4H9)3 In pyridine at 180℃; for 8h; | 40% |
dodecacarbonyl-triangulo-triruthenium; P(C4H9)3 In pyridine at 180℃; for 8h; Product distribution; catalytic decarbonylation of some alkyl formates.; | 40% |
Conditions | Yield |
---|---|
With sodium thiophenolate; thiophenol In acetonitrile for 2h; Product distribution; Further Variations:; Solvents; Substitution; elimination; | A 98% B 1.7% C 99% |
Conditions | Yield |
---|---|
chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium (II) at 100℃; | 100% |
With [RhCl2(p-cymene)]2; bis[2-(diphenylphosphino)phenyl] ether In toluene at 250℃; under 37503.8 Torr; Flow reactor; | 93% |
With Cu1-Mo1/TiO2 In neat liquid at 20℃; for 21h; Catalytic behavior; Inert atmosphere; UV-irradiation; | 82% |
Conditions | Yield |
---|---|
With aluminium(III) triflate at 100℃; for 1h; regioselective reaction; | 100% |
Stage #1: epoxybutene; methanol at 0℃; for 0.5h; Stage #2: With sulfuric acid at 0 - 20℃; for 3h; | 25% |
With boron trifluoride diethyl etherate |
Conditions | Yield |
---|---|
With thionyl chloride at 0 - 20℃; | 100% |
Stage #1: 2,2'-oxybis-acetic acid With thionyl chloride at 20℃; for 8h; Stage #2: methanol | 98% |
With sulfuric acid for 24h; Heating; | 90% |
4-chlorophenylacetic Acid
methanol
(4-chloro-phenyl)-acetic acid methyl ester
Conditions | Yield |
---|---|
With hydrogenchloride for 1h; Heating; | 100% |
With monoammonium 12-tungstophosphate for 12h; Heating; | 98% |
With sulfuric acid at 0 - 5℃; for 4.16667h; Reflux; | 98% |
Conditions | Yield |
---|---|
at 20℃; | 100% |
at 64 - 68℃; for 3.8h; | 98.5% |
at 70℃; for 2h; | 98% |
Conditions | Yield |
---|---|
With hydrogenchloride at 80℃; for 20h; Inert atmosphere; | 100% |
With hydrogenchloride In water at 0℃; Reflux; | 83% |
With hydrogenchloride at 0 - 20℃; Reflux; | 83% |
Conditions | Yield |
---|---|
With boron trifluoride at 65℃; for 0.333333h; | 100% |
With ethenetetracarbonitrile for 48h; Ambient temperature; | 99% |
polyaniline hydrocloride at 70℃; for 24h; | 99% |
Conditions | Yield |
---|---|
With hydrogenchloride for 1h; Heating; | 100% |
With sulfuric acid for 4h; Reflux; | 100% |
With sulfuric acid Heating; | 99% |
Conditions | Yield |
---|---|
With chloro-trimethyl-silane at 20℃; | 100% |
With chloro-trimethyl-silane at 0 - 20℃; | 100% |
With chloro-trimethyl-silane for 16h; Reflux; | 97% |
Conditions | Yield |
---|---|
With boron trifluoride at 65℃; for 0.333333h; | 100% |
With sulfuric acid In dichloromethane Dean-Stark; Heating; | 95% |
With sulfuric acid | 80% |
Conditions | Yield |
---|---|
With hydrogenchloride for 1h; Heating; | 100% |
With ammonium cerium(IV) nitrate at 20℃; for 12h; | 99% |
sulfuric acid for 16h; Heating / reflux; | 97.5% |
methanol
(3,4-Dimethoxyphenyl)acetic acid
methyl (3,4-dimethoxyphenyl)acetate
Conditions | Yield |
---|---|
With sulfuric acid Heating; | 100% |
With thionyl chloride for 18h; | 99% |
With sulfuric acid for 0.5h; Reflux; | 99% |
Conditions | Yield |
---|---|
With boron trifluoride at 65℃; for 0.333333h; | 100% |
With phosphorus trichloride Cooling; | 92% |
With hydrogenchloride |
Conditions | Yield |
---|---|
With boron trifluoride at 65℃; for 0.333333h; | 100% |
at 130℃; for 4h; Temperature; | 99.81% |
With aluminum(III) sulphate octadecahydrate at 110℃; for 0.166667h; Sealed tube; Microwave irradiation; | 97.7% |
Conditions | Yield |
---|---|
With boron trifluoride at 65℃; for 0.333333h; | 100% |
With sulfuric acid Heating; | 98% |
With toluene-4-sulfonic acid for 7h; Reflux; Large scale; | 98.08% |
Conditions | Yield |
---|---|
With boron trifluoride at 65℃; for 0.333333h; | 100% |
With modification of hypercrosslinked supermicroporous polymer (HMP-1) via sulfonation (HMP-1-SO3H) at 24.84℃; for 12h; Green chemistry; | 97% |
With Fe3O4 immobilized thiol functionalized mesoporous silica at 24.84℃; for 20h; | 96% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid for 3h; Heating; | 100% |
With sulfuric acid rt. then reflux; | 73.8% |
With sulfuric acid for 24h; Heating; | 70% |
Conditions | Yield |
---|---|
In dichloromethane for 1h; | 100% |
In dichloromethane at 0℃; for 0.25h; | 100% |
In benzene | 99% |
Conditions | Yield |
---|---|
With hydrogenchloride Heating; | 100% |
With sulfuric acid for 24h; Heating; | 90% |
With acetyl chloride at 40℃; for 3.5h; | 53% |
Conditions | Yield |
---|---|
iron(III) chloride | 100% |
With sulfuric acid In 1,2-dichloro-ethane Fisher esterification; | 100% |
With sulfuric acid In 1,2-dichloro-ethane for 12h; Heating; | 100% |
Conditions | Yield |
---|---|
With hydrogenchloride In water for 5h; Temperature; Time; Reflux; chemoselective reaction; | 100% |
With sulfuric acid for 16h; Kinetics; Reflux; | 97% |
With sulfuric acid for 2h; Reflux; | 97% |
Conditions | Yield |
---|---|
With sulfuric acid Heating; | 100% |
With sulfuric acid for 8h; Heating; | 100% |
With sulfuric acid | 100% |
Conditions | Yield |
---|---|
With thionyl chloride Heating; | 100% |
With sulfuric acid for 8h; Reflux; | 100% |
With sulfuric acid under 760.051 Torr; Reflux; | 100% |
Conditions | Yield |
---|---|
With Dowex 50 W x 8200-400 Heating; | 100% |
With thionyl chloride Ambient temperature; | 100% |
With sulfuric acid at 0℃; for 12h; Darkness; Reflux; | 99% |
Conditions | Yield |
---|---|
With thionyl chloride at 20℃; for 48h; Reflux; | 100% |
Stage #1: methanol With thionyl chloride at 0℃; for 0.166667h; Stage #2: L-alanin at 20℃; for 12h; | 97% |
With thionyl chloride at 8 - 10℃; Reflux; | 96.68% |
Conditions | Yield |
---|---|
With thionyl chloride at 0 - 20℃; for 17h; Inert atmosphere; | 100% |
With thionyl chloride at -20 - 20℃; for 17h; Inert atmosphere; | 100% |
With chloro-trimethyl-silane at 20℃; for 12h; | 97% |
Conditions | Yield |
---|---|
With thionyl chloride at 0 - 20℃; | 100% |
With thionyl chloride at 20℃; Cooling with ice; Inert atmosphere; | 100% |
Stage #1: L-valine With thionyl chloride at 0℃; for 4.16667h; Reflux; Stage #2: methanol | 100% |
Conditions | Yield |
---|---|
With thionyl chloride | 100% |
With thionyl chloride | 100% |
With thionyl chloride at 0 - 20℃; | 94% |
Conditions | Yield |
---|---|
With thionyl chloride for 3h; Heating; | 100% |
Stage #1: methanol; LEUCINE With hydrogenchloride at 20℃; Reflux; Stage #2: With sodium hydrogencarbonate In water pH=7; | 96% |
With hydrogenchloride leucine DL-methyl ester; |
Conditions | Yield |
---|---|
Stage #1: methanol With thionyl chloride at -15 - 0℃; for 1h; Stage #2: L-isoleucine for 3h; Reflux; | 100% |
With hydrogenchloride | 96% |
With thionyl chloride at 0℃; for 12h; Reflux; | 95% |
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