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Cas:108-43-0
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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:108-43-0
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LIDE PHARMACEUTICALS LIMITED is a professional chemicals and APIs leading manufacturer in China. Our core business line covers APIs, Intermediates, Herb extract, etc.
Cas:108-43-0
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inquiryAppearance:white powder Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Organics;Phenol&Thiophenol&Mercaptan;P. Transportation:Common products:Sea/Air/Courier Dan
Cas:108-43-0
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inquirysuperior quality Appearance:White to light yellow crystal. 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:3-Chlorophenol is a halophenol with ant
Minimum 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:108-43-0
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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
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Massive Chemical is certified with ISO9001 and ISO14001 manufacturer for this product. We will offer all documents as requirement for the materials which includes, Certificate of Analysis, Material Safety Data Sheet, and Method of Analysis and
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:108-43-0
Min.Order:10 Gram
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inquiry3-ChlorophenolAppearance:White fine powder Storage:Kept in a cool,dry and ventilated place Package:according to customers' requirements Application:Meets the requirements Transportation:By air(EMS or EUB or FedEx or TNT ect...) or by sea(FOB or CIF o
We are leading fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...)
Cas:108-43-0
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inquiryWe supply high purity 3-chlorophenol CAS#108-43-0 at best price in China, Our 3-chlorophenol CAS#108-43-0 has been exported to many countries and regions. If you are looking for 3-chlorophenol CAS#108-43-0 sppliers in China, Sinosun is your best ch
Cas:108-43-0
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inquiryCAS:108-43-0 EINECS:203-582-6 MW:128.56 MF:C6H5ClO Melting point:31-34 °C(lit.) Boiling point:214 °C(lit.) Appearance:White needle crystals Package:25kg/drum Transportation:by sea/air/courier Port:Shanghai
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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Our company is engaged in customizing the benzene ring and pyridine derivative organic intermediates, and the quantity is flexible according to customer's needs. It mainly provides high-quality intermediates for domestic and foreign pharmaceutical an
Cas:108-43-0
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inquiryhigh 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
R & D enterprises have their own stock in stockAppearance:To be subject to the object Package:Customized Application:pharmaceutical intermediates Transportation:Air Port:Shanghai;Guangzhou
high purity,in stock Package:25kg/drum,or as per customers'demand Application:API,Pharmaceutical intermediates Transportation:air,sea,courier
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:108-43-0
Min.Order:1 Kilogram
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inquiry108-43-0Appearance:white powder Storage:room temperature Application:industry use
Ansciep 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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3-Chlorophenol CAS NO.108-43-0 Application:3-Chlorophenol CAS NO.108-43-0
3-Chlorophenol CAS NO.108-43-0Appearance:White to light yellow crystal Storage:Dry and ventilated Package:Standard or as customer's require Application:Organic Chemicals Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amoun
Cas:108-43-0
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inquiry1-tert-butoxy-3-chlorobenzene
3-monochlorophenol
Conditions | Yield |
---|---|
With sodium iodide; cerium(III) chloride In acetonitrile at 40℃; for 3.5h; | 100% |
1-(benzyloxy)-3-chlorobenzene
3-monochlorophenol
Conditions | Yield |
---|---|
With 1-n-butyl-3-methylimidazolim bromide at 200 - 220℃; for 0.0833333h; Microwave irradiation; Inert atmosphere; | 99% |
With triethylsilane; triethylamine; palladium diacetate In dichloromethane at 23℃; for 12h; Hydrogenolysis; |
Conditions | Yield |
---|---|
With 9,10-dihydroanthracene; water at 356.85℃; for 3h; Kinetics; | A 99% B 0.3% |
Conditions | Yield |
---|---|
With potassium hydroxide; tris-(dibenzylideneacetone)dipalladium(0); tert-butyl XPhos In 1,4-dioxane; water at 100℃; for 1h; | 99% |
Multi-step reaction with 2 steps 1: copper dichloride; potassium carbonate / 20 h / 130 °C / Inert atmosphere; Schlenk technique 2: potassium hydroxide / dimethyl sulfoxide / 3 h / 100 °C / Schlenk technique View Scheme | |
Multi-step reaction with 2 steps 1: fac-tris(2-phenylpyridinato-N,C2')iridium(III); tributyl-amine; water / acetonitrile / 36 h / 25 °C / Schlenk technique; Inert atmosphere; Sealed tube; Irradiation 2: air / 16 h / 25 °C / Inert atmosphere View Scheme | |
With copper(l) iodide; C20H20N4O4; caesium carbonate; Benzaldoxime In dimethyl sulfoxide at 80℃; for 18h; Inert atmosphere; Glovebox; |
3-chlorophenylboronic acid
3-monochlorophenol
Conditions | Yield |
---|---|
With water In tetrahydrofuran at 100℃; for 12h; | 99% |
With copper(I) oxide; potassium hydroxide In water at 20℃; for 24h; Green chemistry; | 98% |
With copper(II) ferrite; water; sodium hydroxide at 40℃; for 24h; Green chemistry; | 96% |
Conditions | Yield |
---|---|
With 1-n-butyl-3-methylimidazolim bromide at 200 - 220℃; for 0.666667h; Microwave irradiation; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With potassium hydroxide In dimethyl sulfoxide at 100℃; for 3h; Schlenk technique; | 99% |
Conditions | Yield |
---|---|
With glycolic Acid; copper hydroxide; sodium hydroxide In water; dimethyl sulfoxide at 120℃; for 6h; Inert atmosphere; Schlenk technique; | 98% |
With copper acetylacetonate; N1-(4-hydroxy-2,6-dimethylphenyl)-N2-(4-hydroxy-3,5-dimethylphenyl)oxalamide; potassium hydroxide In water; dimethyl sulfoxide at 60℃; for 24h; Schlenk technique; Inert atmosphere; chemoselective reaction; | 95% |
With copper(I) oxide; 2-(N,N-dimethylamino)ethanol; water; potassium hydroxide In dimethyl sulfoxide at 110℃; for 24h; Inert atmosphere; | 91% |
Conditions | Yield |
---|---|
With ammonium bicarbonate In water at 20℃; for 2h; Schlenk technique; | 97% |
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; (1,2-dimethoxyethane)dichloronickel(II); water; bis(pinacol)diborane; lithium tert-butoxide In methanol; N,N-dimethyl acetamide at 30℃; for 24h; Schlenk technique; | 92% |
With 6,6'-dimethyl-2,2'-bipyridine; (1,2-dimethoxyethane)dichloronickel(II); bis(pinacol)diborane; lithium tert-butoxide In methanol; N,N-dimethyl acetamide; water at 30℃; for 24h; Inert atmosphere; Glovebox; Sealed tube; | 92% |
3-monochlorophenol
Conditions | Yield |
---|---|
With tert.-butyl lithium In tetrahydrofuran; pentane at -78℃; for 0.5h; | 91% |
(1S,2S)-3-Chloro-cyclohexa-3,5-diene-1,2-diol
A
3-monochlorophenol
B
2-monochlorophenol
Conditions | Yield |
---|---|
With sodium hydroxide In water at 25℃; Kinetics; Concentration; Solvent; | A 89% B n/a |
3-chlorophenyl N,N-diethylcarbamate
3-monochlorophenol
Conditions | Yield |
---|---|
With zirconocene dichloride In tetrahydrofuran at 20℃; Inert atmosphere; | 88% |
Conditions | Yield |
---|---|
85% |
Conditions | Yield |
---|---|
With [Ni(N,N-bis(4-methoxy-3,5-dimethylpyridin-2-ylmethyl)-N',N'-dimethylpropane-1,3-diamine)(CH3CN)2](Ph4B)2; dihydrogen peroxide; triethylamine In water; acetonitrile at 60℃; for 5h; | A 16% B 84% |
With C25H29N7O*Fe(2+)*2CF3O3S(1-); dihydrogen peroxide | |
With dihydrogen peroxide; C23H37ClCuN4O6(1+)*ClO4(1-); triethylamine In acetonitrile at 60℃; for 5h; |
Conditions | Yield |
---|---|
Stage #1: m-Chlorobenzaldehyde With 3-chloro-benzenecarboperoxoic acid for 0.0833333h; Dakin oxidation; Stage #2: With sodium hydroxide for 0.0833333h; Further stages.; | 80% |
1-(but-3-enyloxy)-3-chlorobenzene
3-monochlorophenol
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; (1,2-dimethoxyethane)dichloronickel(II); water; bis(pinacol)diborane; lithium tert-butoxide In methanol; N,N-dimethyl acetamide at 30℃; for 24h; Schlenk technique; | 75% |
With 6,6'-dimethyl-2,2'-bipyridine; (1,2-dimethoxyethane)dichloronickel(II); bis(pinacol)diborane; lithium tert-butoxide In methanol; N,N-dimethyl acetamide; water at 30℃; for 24h; Inert atmosphere; Glovebox; Sealed tube; | 75% |
Conditions | Yield |
---|---|
Stage #1: 3-chloro-aniline With sodium nitrite In water at 20℃; Milling; Green chemistry; Stage #2: With water at 85℃; for 0.5h; Neutral conditions; Green chemistry; | 73% |
With uranyl nitrate hydrate; water; trifluoroacetic acid for 48h; Irradiation; | 56% |
diethyl phosphite potassium salt
3-chloro-1-trifluoromethanesulfonyloxybenzene
A
3-monochlorophenol
B
3-chlorophenyl diethyl phosphate
Conditions | Yield |
---|---|
In ammonia at -33℃; under 2.5 Torr; | A 30% B 67% |
Conditions | Yield |
---|---|
With 9,10-dihydroanthracene; water at 356.85℃; for 3h; Kinetics; | A 62% B 0.3% |
α-(3-Chlorophenoxy)acetophenone
A
3-monochlorophenol
B
2-oxo-2-phenyl-ethyl
C
2-(3-chlorophenyl)-1-phenylethanone
D
3-chlorophenoxyl radical
E
acetophenone
Conditions | Yield |
---|---|
thiophenol In benzene Product distribution; Quantum yield; Kinetics; Irradiation; | A 34.2% B n/a C 42.1% D n/a E 23.8% |
chlorobenzene
A
3-monochlorophenol
B
2-monochlorophenol
C
4-chloro-phenol
D
phenol
Conditions | Yield |
---|---|
With KCu(III)(biuret)2; water; trifluoroacetic acid for 2h; Product distribution; Heating; | A n/a B 6% C 7% D 33% |
With tert.-butylhydroperoxide; air In gas at 290℃; under 760 Torr; Product distribution; Mechanism; | |
In tert-butyl alcohol at 488 - 587℃; under 760 Torr; Mechanism; Slow combustion of dichlorobenzene has been studied at low degrees of conversion at low degrees of conversion, in athmospheric pressure, between 410-1053 K , in various solvents.; | |
cyclohexa-1,3-diene at 570 - 622℃; under 760 Torr; Mechanism; | |
With air at 686.85℃; Formation of xenobiotics; Further byproducts given. Title compound not separated from byproducts; |
3-chlorobenzenediazonium
3-monochlorophenol
Conditions | Yield |
---|---|
With sulfuric acid Diazotization.Behandlung der Diazoniumsalz-Loesung mit CuOH; |
Conditions | Yield |
---|---|
With sodium hydroxide at 260℃; | |
With sodium hydroxide at 200℃; | |
With methanol; sodium methylate at 180℃; | |
With sodium methylate; sodium thiomethoxide 1.) HMPA, 120 degC, 2h; 2.) 120 degC, 1h; Yield given. Multistep reaction; |
2,2,2-trifluoroethanol
A
3-monochlorophenol
B
(2,2,2-trifluoroethoxy)dimethylphenylsilane
Conditions | Yield |
---|---|
With potassium 2,2,2-trifluoroethoxide at 30℃; Rate constant; μ = 0.05 M with potassium trifluoroacetate; |
4-chloro-2-hydroxybenzophenone
A
3-monochlorophenol
B
3-chlorophenyl benzoate
Conditions | Yield |
---|---|
trifluorormethanesulfonic acid In 1,2-dichloro-ethane at 170℃; for 24h; Mechanism; Product distribution; in dependence on concentration of TFMS, time; | A 5.1 % Chromat. B 47.7 % Chromat. |
1-chloro-3-methylbenzene
A
3-monochlorophenol
B
m-chlorobenzyl alcohol
C
3-Chlorobenzaldehyde
D
3-chlorobenzoate
Conditions | Yield |
---|---|
With water; iron; trifluoroacetic acid In acetone for 1h; Rate constant; | |
With water; iron; trifluoroacetic acid In pyridine for 1h; Rate constant; | |
With water; copper; trifluoroacetic acid In pyridine for 1h; Rate constant; | |
With water; copper; trifluoroacetic acid In acetone for 1h; Rate constant; |
3-chlorophenyl acetate
3-monochlorophenol
Conditions | Yield |
---|---|
With N-butylamine; Tetraethylene glycol dimethyl ether In chlorobenzene at 25℃; Rate constant; efficacy of glyme catalysis, other glymes; | |
With potassium chloride; poly(ethyleneimine) In water at 25℃; Rate constant; Mechanism; Product distribution; various pH, aminolysis; |
3-monochlorophenol
(2E)-3-ethoxyprop-2-enoyl chloride
3-Ethoxyacrylsaeure-3-chlorphenylester
Conditions | Yield |
---|---|
In 1,2-dichloro-ethane for 14h; Heating; | 100% |
3-monochlorophenol
propargyl bromide
1-chloro-3-(prop-2-yn-1-yloxy)benzene
Conditions | Yield |
---|---|
With potassium carbonate In acetone Reflux; | 100% |
With potassium carbonate In N,N-dimethyl-formamide; toluene at 60℃; for 16h; Sealed tube; Inert atmosphere; | 95% |
With potassium carbonate In acetone at 56℃; | 93% |
3-monochlorophenol
N,N-diethylcarbamyl chloride
3-chlorophenyl N,N-diethylcarbamate
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 70℃; for 13.5h; | 100% |
Stage #1: 3-monochlorophenol With sodium hydride In tetrahydrofuran; mineral oil at 23℃; for 1h; Inert atmosphere; Stage #2: N,N-diethylcarbamyl chloride In tetrahydrofuran; mineral oil at 23℃; for 16h; Inert atmosphere; | 94% |
Stage #1: 3-monochlorophenol With sodium hydride In tetrahydrofuran for 1.16667h; Stage #2: N,N-diethylcarbamyl chloride In tetrahydrofuran at 20℃; for 14h; | 93% |
3-monochlorophenol
3-chloro-4-fluoronitrobenzene
2-chloro-1-(3-chlorophenoxy)-4-nitrobenzene
Conditions | Yield |
---|---|
Stage #1: 3-monochlorophenol; 3-chloro-4-fluoronitrobenzene With caesium carbonate In N,N-dimethyl-formamide; acetonitrile at 20℃; Stage #2: With water In N,N-dimethyl-formamide; acetonitrile | 100% |
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 2h; |
3-monochlorophenol
benzyl 3-[4-(5-methanesulfonyloxazolo[5,4-d]pyrimidin-2-yl)-2,6-dimethylphenoxy]cyclobutanecarboxylate
benzyl 3-{4-[5-(3-chlorophenoxy)oxazolo[5,4-d]pyrimidin-2-yl]-2,6-dimethylphenoxy}cyclobutanecarboxylate
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20 - 60℃; for 5.5h; | 100% |
3-monochlorophenol
4-Fluoronitrobenzene
1-chloro-3-(4-nitrophenoxy)benzene
Conditions | Yield |
---|---|
With cesium fluoride/clinoptilolite In dimethyl sulfoxide at 110℃; for 0.15h; Ullmann Condensation; | 100% |
With potassium carbonate In dimethyl sulfoxide at 70℃; | 92% |
With potassium carbonate In acetonitrile at 90℃; for 18h; |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 1.5h; Inert atmosphere; | 100% |
3-monochlorophenol
Conditions | Yield |
---|---|
With caesium carbonate In acetonitrile at 0 - 20℃; | 100% |
3-monochlorophenol
2-chloroethyl cyanomethyl ether
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl acetamide at 120℃; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With hydrogen; sodium hydroxide In water at 25℃; for 2h; | 99.9% |
With hydrogen; sodium hydroxide In water at 20℃; under 760.051 Torr; for 1h; | 99.9% |
With hydrogen; sodium hydroxide In water at 20℃; under 760.051 Torr; for 1.5h; | 99.8% |
3-monochlorophenol
2,4,6-tribromo-3-chlorophenol
Conditions | Yield |
---|---|
With benzyltrimethylammonium tribromide; calcium carbonate In methanol; dichloromethane | 99% |
With water; potassium bromide |
Conditions | Yield |
---|---|
With Zn(N4,N4'-di(pyridin-4-yl)biphenyl-4,4'-dicarboxamide)(5-aminoisophthalate) In dichloromethane at 20℃; for 14h; | 99% |
With sulfuric acid at 20℃; for 17h; | 99% |
With C36H30N4O4*2C3H7NO*2NO3(1-)*Zn(2+)*2C2H3N In dichloromethane at 20℃; for 11h; | 97% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 4h; Reflux; | 99% |
With potassium carbonate In acetone for 20h; Reflux; | 98% |
With hydrogenchloride; potassium carbonate In hexane; ethyl acetate; acetone | 58 g (87%) |
3-monochlorophenol
3-(diphenylphosphinyl)-3-methyl-1,2-butadiene
C22H20ClO2P
Conditions | Yield |
---|---|
With (R)-((4,4’-bi-1,3-benzodioxole)-5,5’-diyl)bis(bis(3,5-di-t-butyl-4-methoxyphenyl))phosphine; [Rh(OH)(cod)]2 In tert-butyl alcohol at 80℃; for 24h; Inert atmosphere; optical yield given as %ee; enantioselective reaction; | 99% |
N-(2-nitro-5-chlorophenyl)-N-methylcarbamic acid t-butyl ester
3-monochlorophenol
tert-butyl [5-(3-chlorophenoxy)-2-nitrophenyl]methylcarbamate
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl acetamide at 80℃; Cooling with ice; | 99% |
With sodium hydride In N,N-dimethyl-formamide at 80℃; for 10h; Inert atmosphere; | 99% |
3-monochlorophenol
Phenyl glycidyl ether
1-(3'-chlorophenoxy)-3-phenoxypropan-2-ol
Conditions | Yield |
---|---|
With 2-tert-butylimino-2-diethylamino-1,3-dimethylperhydro-1,3,2-diazaphosphorine supported on polystyrene (PS-BEMP; PS = 200-400 mesh polystyryl with 2percent of divinylbenzene) at 60℃; for 40h; Neat (no solvent); regioselective reaction; | 99% |
3-monochlorophenol
2-fluoro-4-methoxy-benzaldehyde
2-(3-chlorophenoxy)-4-methoxybenzaldehyde
Conditions | Yield |
---|---|
With potassium carbonate In dimethyl sulfoxide at 120℃; for 3h; Inert atmosphere; | 99% |
3-monochlorophenol
4-fluorobenzonitrile
4-(3-chlorophenoxy)benzoic acid
Conditions | Yield |
---|---|
Stage #1: 3-monochlorophenol; 4-fluorobenzonitrile With potassium hydroxide In N,N-dimethyl-formamide at 175℃; for 0.333333h; Sealed tube; Stage #2: With potassium hydroxide In water for 12h; Reflux; | 99% |
Stage #1: 3-monochlorophenol; 4-fluorobenzonitrile With potassium hydroxide In N,N-dimethyl-formamide at 175℃; for 0.333333h; Sealed tube; Stage #2: With water; potassium hydroxide for 12h; Reflux; | 99% |
3-monochlorophenol
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 100℃; for 18h; Temperature; | 99% |
3-monochlorophenol
3,5-dibromo-1-methyl-1H-1,2,4-triazole
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 100℃; for 15h; Sealed tube; | 99% |
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