Product name: 2,6-Dichlorophenol CAS No.: 87-65-0 Molecule Formula:C6H4OCl2 Molecule Weight:163.00 Purity: 99.0% Package: 50kg/drum Description:White acicular crystals powder Manufacture Standards:Enterprise Standard
Cas:87-65-0
Min.Order:1 Kilogram
Negotiable
Type:Trading Company
inquiryDayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:87-65-0
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
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Cas:87-65-0
Min.Order:1 Metric Ton
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inquiryInspection Item Standard Regulation Inspection Data 2,6-Dichlorophenol (%) ≥99.5 99.55
Cas:87-65-0
Min.Order:1 Gram
FOB Price: $100.0 / 500.0
Type:Manufacturers
inquiryProduct description: Product name 2,6-Dichlorophenol CAS number 87-65-0 Assay ≥99% Appearance White crystalline powder Capacity 2000mt/year Application Dye/pesticide/pharmace
Cas:87-65-0
Min.Order:10 Gram
FOB Price: $12.0
Type:Lab/Research institutions
inquiryHebei Yanxi Chemical Co., Ltd. is a professional research, development and production of lead acetate benzene acetamide enterprise backbone members by local well-known entrepreneurs and professional senior engineers in the party's "low car
Cas:87-65-0
Min.Order:1 Metric Ton
FOB Price: $1.0 / 2.0
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
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Cas:87-65-0
Min.Order:5 Kiloliter
FOB Price: $1.2 / 5.0
Type:Manufacturers
inquiryOur 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 Scientific and so on.O
2,6-Dichlorophenol Chinese alias:2,6-Dichlorfenol Molecular formula:C6H4Cl2O M
1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; Appearance:white or off-white powder Storage:Store in sealed containers
Cas:87-65-0
Min.Order:100 Gram
Negotiable
Type:Other
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
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Cas:87-65-0
Min.Order:1 Kilogram
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
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:87-65-0
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquirySuperior quality, moderate price & quick delivery. Appearance:colorless needle-like crystals Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum, or as per your request. Application:For medicine , pestic
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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SAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in custom synthe
Cas:87-65-0
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryCapability on chemical synthesis1. Beijing High-Tech Enterprises2. Strong R&D Team3. 8 years of experiences in R & D of high-tech Catalyst;4. 5000 production techniques, 69 items of national patents, and 360 kinds of products on sales;5. The producti
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,Pharmaceutical intermediates 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
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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:87-65-0
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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2,6-Dichlorophenol cas 87-65-0Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
tert-butyl (2,6-dichlorophenoxy)dimethylsilane
2,6-Dichlorophenol
Conditions | Yield |
---|---|
With lithium acetate In water; N,N-dimethyl-formamide at 70℃; for 3h; Inert atmosphere; | 94% |
Conditions | Yield |
---|---|
With 2,2,6,6-tetramethyl-piperidine; sulfuryl dichloride In toluene at 25℃; for 24h; Inert atmosphere; regioselective reaction; | 91% |
With 1,3-dichloro-5,5-dimethylhydantoin; diisopropylamine hydrochloride In toluene at 0℃; for 4h; Darkness; regioselective reaction; | 78% |
With tetrachloromethane; tert-butylhypochlorite |
Conditions | Yield |
---|---|
With copper(I) oxide In quinoline at 220℃; for 6h; Autoclave; | 86% |
With quinoline at 190℃; | |
With methyllithium; calcium carbonate |
Conditions | Yield |
---|---|
With selenium(IV) oxide; dihydrogen peroxide In tetrahydrofuran for 52h; Heating; | A 4 % Chromat. B 86% |
Conditions | Yield |
---|---|
With iron(III) chloride; diphenyl sulfide; boric acid at 40 - 80℃; | A 13.31% B 85.43% |
With chloroamine In water pH=9.0; Product distribution; Further Variations:; Reagents; pH-values; | A 23% B 77% |
With N-chlorobis(2-chloroethyl)amine; silica gel In tetrachloromethane at 25℃; Yield given. Yields of byproduct given; | |
With 2,3,4,4,5,6-hexachlorocyclohexa-2,5-dien-1-one In tetrachloromethane; N,N-dimethyl-formamide at 20℃; for 360h; other reagent; Yield given. Yields of byproduct given; | |
With aluminum (III) chloride; sulfuryl dichloride In neat (no solvent) at 25 - 55℃; for 3h; Reagent/catalyst; Temperature; regioselective reaction; | A 5.7 %Chromat. B 92.1 %Chromat. |
Conditions | Yield |
---|---|
With triethylamine In toluene at 80℃; for 2.5h; Reagent/catalyst; Solvent; Time; | 84.4% |
With triethylamine In N,N-dimethyl-formamide at 100℃; for 4h; Dehydrochlorination; | 30% |
Conditions | Yield |
---|---|
With 12-TPA/SBA 15 In 1,4-dioxane at 110℃; | 75% |
2,6-dichlorophenylboronic acid
2,6-Dichlorophenol
Conditions | Yield |
---|---|
With ozone In ethanol; water at 20 - 30℃; for 0.583333h; | 73% |
2,6-Dichlorophenol
Conditions | Yield |
---|---|
With 12-TPA/SBA 15 In 1,4-dioxane at 110℃; | 70% |
phenol
A
2,6-Dichlorophenol
B
4-chloro-phenol
C
2,4-dichlorophenol
Conditions | Yield |
---|---|
With hydrogenchloride; sodium chlorate In water; acetic acid at 20℃; for 72h; | A 4% B 16% C 65% |
phenol
A
2,6-Dichlorophenol
B
2-monochlorophenol
C
4-chloro-phenol
D
2,4-dichlorophenol
E
2,4,6-Trichlorophenol
Conditions | Yield |
---|---|
With aluminium trichloride; diphenyl sulfide; chlorine In neat (no solvent) at 35℃; for 1.5h; Product distribution; others 2-alkylphenols; var. chlorinating agent, temp., and time; | A 0.5% B 18.4% C 58.6% D 7.7% E 0.5% |
With N,N'-dichloropiperazine; silica gel In tetrachloromethane at 25℃; Product distribution; further reagents; | |
With tert-butylhypochlorite; tris(3-pyridiniumprop-1-yl)benzene-1,3,5-tricarboxylatetrichloride In acetonitrile Product distribution; Mechanism; other tentacle reagents and variations of concentration; | |
With tert-butylhypochlorite; cetylpyridinium chloride In water Product distribution; other reagents and solvent; | |
With sulfuryl dichloride; 2-aminopyridine In toluene at 70℃; for 1h; Product distribution; chlorination catalyzed by var. amines under var. conditions; | A n/a B 32.3 % Chromat. C 60.3 % Chromat. D n/a E n/a |
phenol
A
2,6-Dichlorophenol
B
2-monochlorophenol
C
4-chloro-phenol
D
2,4-dichlorophenol
Conditions | Yield |
---|---|
With chloroamine In water pH=9.0; Product distribution; Further Variations:; Reagents; pH-values; | A 9.6% B 50.5% C 23% D 16.3% |
With oxygen; silica gel; copper dichloride at 200℃; Formation of xenobiotics; | A 0.004% B 4.761% C 1.149% D 0.393% |
With oxygen; silica gel; copper dichloride at 225℃; Formation of xenobiotics; Further byproducts.; | A 0.008% B 3.892% C 0.998% D 0.394% |
2,6-dichlorophenyl dimethylcarbamate
2,6-Dichlorophenol
Conditions | Yield |
---|---|
With hydrazine hydrate at 60℃; for 2h; Sealed tube; regioselective reaction; | 50% |
Conditions | Yield |
---|---|
With hydrogenchloride; potassium permanganate In acetonitrile at 60℃; | A 44% B 44% |
With alkaline sodium hypochlorite solution | |
With chlorine |
Conditions | Yield |
---|---|
With sodium methylate In N,N,N,N,N,N-hexamethylphosphoric triamide at 120℃; | 33% |
1,2,3-trichlorobenzene
A
2,6-Dichlorophenol
B
2,3-dichloroanisole
C
2,6-dichloroanisole
Conditions | Yield |
---|---|
With potassium hydroxide; Tris(3,6-dioxaheptyl)amine at 135℃; for 2h; | A 23% B 756 g C 496 g |
2-nitropropane
2,6-dichloro-4-dimethylaminomethyl-phenol
A
2,6-Dichlorophenol
B
3,5-dichloro-4-hydroxybenzaldehyde
C
2,6-Dichlor-4-(2-methyl-2-nitropropyl)phenol
Conditions | Yield |
---|---|
potassium fluoride; tetrabutyl-ammonium chloride for 30h; Heating; | A n/a B n/a C 12% |
2-monochlorophenol
A
dioxin
B
2,6-Dichlorophenol
C
1-chlorodibenzo-p-dioxin
Conditions | Yield |
---|---|
With oxygen at 600℃; for 0.000555556h; Product distribution; Further Variations:; Temperatures; | A 1.32% B 0.59% C 0.92% D 9.43% |
2-monochlorophenol
A
dioxin
B
2,6-Dichlorophenol
C
1-chlorodibenzo-p-dioxin
D
2,4-dichlorophenol
Conditions | Yield |
---|---|
With oxygen; silica gel; copper dichloride at 400℃; Product distribution; Further Variations:; Temperatures; | A 0.6915% B 0.219% C 0.7511% D 0.238% |
With oxygen; silica gel; copper dichloride at 350℃; Formation of xenobiotics; Further byproducts.; | A 0.0672% B 0.229% C 0.3293% D 0.282% |
2-monochlorophenol
A
2,6-Dichlorophenol
B
2,4-dichlorophenol
C
2,4,6-Trichlorophenol
Conditions | Yield |
---|---|
With oxygen; silica gel; copper dichloride at 300℃; Formation of xenobiotics; | A 0.282% B 0.379% C 0.128% |
With N-chloro-succinimide at 80℃; for 10h; regioselective reaction; | A 8 %Chromat. B 55 %Chromat. C 18 %Chromat. |
2-monochlorophenol
A
2,6-Dichlorophenol
B
1-chlorodibenzo-p-dioxin
C
2,4-dichlorophenol
D
2,4,6-Trichlorophenol
Conditions | Yield |
---|---|
With oxygen; silica gel; copper dichloride at 325℃; Formation of xenobiotics; | A 0.257% B 0.0024% C 0.312% D 0.053% |
Conditions | Yield |
---|---|
at 190 - 200℃; | |
at 190℃; |
Conditions | Yield |
---|---|
With palladium on activated charcoal; sodium acetate; benzene Hydrogenation.Reagens 4: Cyclohexan; | |
With sodium sulfite In water at 130℃; Sealed tube; Microwave irradiation; Green chemistry; | 63 mg |
4-tert-butyl-2,6-dichloro-phenol
2,6-Dichlorophenol
Conditions | Yield |
---|---|
With aluminium trichloride; xylene |
Conditions | Yield |
---|---|
With sulfuric acid Diazotization.Kochen des Diazoniumsulfats mit Wasser und Soda; |
2,6-dichloro-4-tert-pentyl-phenol
2,6-Dichlorophenol
Conditions | Yield |
---|---|
With aluminium trichloride; xylene at 65 - 95℃; | |
With boron trifluoride; xylene at 60℃; |
3,5-dichloro-4-hydroxybenzoic acid
N,N-dimethyl-aniline
2,6-Dichlorophenol
Conditions | Yield |
---|---|
at 190℃; |
methanol
sodium methylate
1,2,3-trichlorobenzene
A
2,6-Dichlorophenol
B
2,3-dichloroanisole
C
2,3-dichlorophenol
Conditions | Yield |
---|---|
at 180℃; im Rohr; |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide for 2h; Heating; | 100% |
2,6-Dichlorophenol
trifluoromethylsulfonic anhydride
2,6-dichlorophenyl trifluoromethanesulphonate
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 0 - 20℃; | 100% |
Conditions | Yield |
---|---|
With palladium diacetate; dicyclohexylphenylphosphine In water; 1,2-dichloro-ethane at 40 - 70℃; for 3h; Reagent/catalyst; Solvent; Temperature; Concentration; Suzuki Coupling; Inert atmosphere; Sealed tube; | 99.3% |
With C28H44N2PPd; potassium carbonate In ethanol; water at 60℃; for 6h; Suzuki coupling; | 96% |
With reduced graphene oxide/Pd-Fe3O4(at)polypyrrole nanocomposite In water at 70℃; for 3h; Suzuki Coupling; Sonication; | 65% |
2,6-Dichlorophenol
4-(4-nitrophenyl)-1-piperazinecarbonyl chloride
C17H15Cl2N3O4
Conditions | Yield |
---|---|
Stage #1: 2,6-Dichlorophenol With sodium hydride In tetrahydrofuran for 0.25h; Molecular sieve; Stage #2: 4-(4-nitrophenyl)-1-piperazinecarbonyl chloride In tetrahydrofuran at 20℃; for 18.5h; Heating / reflux; | 99% |
Stage #1: 2,6-Dichlorophenol With sodium hydride In tetrahydrofuran for 0.25h; Stage #2: 4-(4-nitrophenyl)-1-piperazinecarbonyl chloride In tetrahydrofuran at 20℃; for 19h; Heating / reflux; | 99% |
Conditions | Yield |
---|---|
In [D3]acetonitrile at 20℃; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With Zn(NO3)2*2N2O4 In dichloromethane at 20℃; for 0.0833333h; | 98% |
With tetra(n-butyl)ammonium dichromate(VI); sodium nitrite In dichloromethane for 23h; Reflux; chemoselective reaction; | 98% |
With Tetraethylene glycol; silica gel; dinitrogen tetraoxide In dichloromethane at 20℃; for 0.0833333h; | 97% |
2,6-Dichlorophenol
A
2,6-Dichlorophenyl sulfate
Conditions | Yield |
---|---|
With sulfur trioxide In nitromethane-d3 at -30℃; for 0.0333333h; Product distribution; various solvents, times, temperatures, amounts of SO3; | A 98% B 2% |
Conditions | Yield |
---|---|
With 1-methyl-1H-imidazole; N,N,N,N,-tetramethylethylenediamine In acetonitrile at 0 - 5℃; for 1h; | 98% |
2,6-Dichlorophenol
3-chloro-1-(4-fluorophenyl)-1-propanol
1-(4-fluorophenyl)-1-(2,6-dichlorophenoxy)-3-chloropropane
Conditions | Yield |
---|---|
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran; toluene at 20℃; Inert atmosphere; | 98% |
2,6-Dichlorophenol
3-chloro-1-(p-tolyl)propan-1-ol
1-(4-methylphenyl)-1-(2,6-dichlorophenoxy)-3-chloropropane
Conditions | Yield |
---|---|
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran; toluene at 20℃; Inert atmosphere; | 98% |
2,6-Dichlorophenol
tert-butyldimethylsilyl chloride
tert-butyl (2,6-dichlorophenoxy)dimethylsilane
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide at 0 - 20℃; | 98% |
With 1H-imidazole In N,N-dimethyl-formamide at 0 - 20℃; | 98% |
2,6-Dichlorophenol
2,6-dichloro-4-iodophenol
Conditions | Yield |
---|---|
Stage #1: 2,6-Dichlorophenol With ethylenediamine; sodium iodide In ethanol; water for 0.25h; Stage #2: With iodine In ethanol; water at 20℃; | 97% |
With dihydrogen peroxide; iodine In water for 0.75h; Sonication; | 97% |
With dihydrogen peroxide; iodine In water at 50℃; for 24h; regioselective reaction; | 95% |
Conditions | Yield |
---|---|
With bromine In acetonitrile at 0℃; for 6h; | 97% |
With bromine In acetonitrile at 0℃; for 2h; | 95.5% |
With bromine In acetonitrile at 0℃; for 2h; | 94% |
Conditions | Yield |
---|---|
With N,N'-dimethylimidazolium-2-carboxylate In acetonitrile at 160℃; for 2h; Microwave irradiation; Green chemistry; | 97% |
Conditions | Yield |
---|---|
Stage #1: (2-benzoylamino-phenyl)-acetic acid methyl ester With thionyl chloride for 3h; Reflux; Stage #2: 2,6-Dichlorophenol With potassium carbonate In toluene for 3h; Reagent/catalyst; Cooling with ice; Reflux; | 97% |
2,6-Dichlorophenol
(R)-2-(4-hydroxybutan-2-yl)isoindoline-1,3-dione
(R)-2-(4-(2,6-dichlorophenoxy)butan-2-yl)isoindoline-1,3-dione
Conditions | Yield |
---|---|
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 0 - 20℃; | 96% |
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 0 - 20℃; for 17h; | 96% |
Conditions | Yield |
---|---|
With 1,4-diaza-bicyclo[2.2.2]octane In neat (no solvent) at 70 - 140℃; for 0.183333h; Microwave irradiation; | 96% |
Conditions | Yield |
---|---|
With tris(2,2'-bipyridyl)ruthenium dichloride In acetonitrile at 20℃; for 3h; Irradiation; | 96% |
Conditions | Yield |
---|---|
aluminium dodecatungsten phosphate at 20℃; for 0.25h; | 95% |
With o-benzenedisulfonimide at 20℃; for 4h; | 95% |
With pentaaminechlorocobalt(III) dichloride; phosphoric acid In neat (no solvent) at 75℃; for 0.166667h; Reagent/catalyst; Green chemistry; chemoselective reaction; | 90% |
In 1,4-dioxane; water at 25℃; Rate constant; Anion, pH 7.50; | |
With pyridine |
2,6-Dichlorophenol
[2-(2,6-dichloroanilino)phenyl]acetic acid
Conditions | Yield |
---|---|
With potassium hydroxide In dimethyl sulfoxide at 60 - 100℃; for 8h; Temperature; Reagent/catalyst; | 95% |
Conditions | Yield |
---|---|
With sodium hydroxide In neat (no solvent) at 90℃; for 5h; Green chemistry; | 95% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 2.5h; | 94.1% |
With triethylamine In dichloromethane at 0 - 20℃; for 2.5h; Inert atmosphere; | 94% |
With triethylamine In dichloromethane at 20℃; for 2.5h; | 94% |
Conditions | Yield |
---|---|
Stage #1: 2,6-Dichlorophenol With potassium carbonate In dimethyl sulfoxide at 20℃; Inert atmosphere; Stage #2: allyl bromide In dimethyl sulfoxide at 20℃; for 2h; Inert atmosphere; regioselective reaction; | 94% |
With potassium carbonate; butanone | |
With potassium carbonate |
2,6-Dichlorophenol
methyl 3,3,3-trifluoropyruvate
Conditions | Yield |
---|---|
With triethylamine In benzene for 6h; Ambient temperature; | 94% |
2,6-Dichlorophenol
2-chloro-N-(2-(3,4-dimethoxyphenyl)ethyl)acetamide
2-(2,6-dichloro-phenoxy)-N-[2-(3,4-dimethoxy-phenyl)-ethyl]-acetamide
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile for 6h; Heating; | 94% |
2,6-Dichlorophenol
2-(3-bromopropyl)isoindole-1,3-dione
2-(3-(2,6-dichlorophenoxy)propyl)isoindoline-1,3-dione
Conditions | Yield |
---|---|
With tetra-(n-butyl)ammonium iodide; caesium carbonate In tetrahydrofuran at 20 - 50℃; for 16h; | 94% |
With tetra-(n-butyl)ammonium iodide; caesium carbonate In tetrahydrofuran at 20 - 50℃; for 16h; | 94% |
With potassium carbonate In N,N-dimethyl-formamide at 100℃; for 4h; | |
With potassium carbonate In N,N-dimethyl-formamide at 100℃; |
2,6-Dichlorophenol
4,5-dichloro-2-chloromethyl-pyridazin-3(2H)-one
4-chloro-5-(2,6-dichlorophenoxy)-2-[(2,6-dichlorophenoxy)-methyl]pyridazin-3(2H)-one
Conditions | Yield |
---|---|
With potassium carbonate In methanol for 5h; Reflux; | 94% |
2,6-Dichlorophenol
pentaphenylantimony
2,6-dichlorophenoxytetraphenylstiborane
Conditions | Yield |
---|---|
In toluene room temperature; | 93% |
Conditions | Yield |
---|---|
With N,N-dimethyl-aniline In toluene Inert atmosphere; | 93% |
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