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Cas:10226-30-9
Min.Order:1 Kilogram
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Type:Lab/Research institutions
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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Type:Manufacturers
inquiry6-Chloro-2-hexanone Basic information Product Name: 6-Chloro-2-hexanone Synonyms: 1-CHLORO-5-HEXANONE;1-CHLOROHEXAN-5-ONE;4-CHLOROBUTYL METHYL KETONE;6-CHLOROHEXAN-2-ONE;6-CHLORO-2-H
Cas:10226-30-9
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryOur Advantage Rich Experience Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. Quality service Company cooperates with research institutes. We strictly con
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Min.Order:1 Kilogram
FOB Price: $139.0 / 210.0
Type:Trading Company
inquiryProduct Name: 6-Chloro-2-hexanone Synonyms: 1-CHLORO-5-HEXANONE;1-CHLOROHEXAN-5-ONE;4-CHLOROBUTYL METHYL KETONE;6-CHLOROHEXAN-2-ONE;6-CHLORO-2-HEXANONE;1-Chlorohexane-5-one;Chlorohexanone;6-CHLORO-2-HEXANON
Appearance:Clear yellow to brown liquid Storage:room temperature Package:200kg/drum Application:Chemicals Transportation:Express/Sea/Air Port:Shanghai
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryAdvantages: Hubei XinRunde Chemical Co., Ltd is a renowned pharmaceutical manufacturer. We can offer high quality products at competitive price in quick delivery with 100% custom pass guaranteed. Never stop striving to offer our best s
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Min.Order:10 Gram
Negotiable
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Min.Order:1 Kilogram
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inquiry6-Chloro-2-hexanone CAS:10226-30-9 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic inter
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Min.Order:1 Gram
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
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Min.Order:1 Kilogram
Negotiable
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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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Min.Order:1 Kilogram
Negotiable
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inquiry1. Timely and efficient service to ensure communication with customers 2. Produce products of different specifications and sizes according to your requirements. 3. Quality procedures and standards recognized by SGS. Advanced plant equipment ensures s
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
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
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
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Min.Order:1 Kilogram
FOB Price: $10.0
Type:Trading Company
inquiryZibo 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
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Min.Order:10 Gram
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Type:Lab/Research institutions
inquirySuperior quality, moderate price & quick delivery. Appearance:colorless oil liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:10g/bag,or as your request Application:For medicine , pesticide intermedi
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,
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Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryOur Advantages A. International Top level TechnologyOur company owned biomedicine experts are famous at home and abroad with rich experience in research and development in the field of efficient chiral functional molecules research and development an
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factory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
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Min.Order:1 Kilogram
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Type:Trading Company
inquiryShandong Mopai Biotechnology 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 chemicals. W
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Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiry1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
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Min.Order:1 Metric Ton
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Type:Trading Company
inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
High quality,stable supply chain.Appearance:white/off-white or light yellow Storage:Store in cool and dry place, keep away from strong light and heat. Package:aluminum bottle,glass bottle,PTFE bottle,cardboard drum Application:This product can be use
GOLDEN PHARMA CO.,LIMITED.is a professional pharmaceutical company,our team have more than 20years expereince in pharmaceutical production and sales. we are a professional technical enterprise specializing in the R & D, production,QA regulation
We are a Union of chemistry in China, consists of chemists,engineers, laboratories,factories in China. We organize surplus capacity of R&D and production as well as custom synthesis for chemical products and chemical business project. We are supp
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Type:Trading Company
inquiry1-methylcyclopentanol
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; iron(II) sulfate In tetrachloromethane Ambient temperature; in the dark; | 100% |
With lead(IV) acetate; lithium chloride at 20 - 35℃; for 4h; Oxidation; oxidative decyclization; mechanical activation; | 51% |
(i) aq. NaOCl, (ii) AgNO3, NaOH, aq. NH3; Multistep reaction; |
6-chlorohexene
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With copper(l) iodide; oxygen; palladium dichloride In water; N,N-dimethyl-formamide for 48h; | 99% |
1-chloro-5-hexyne
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With (cyclohexylisocyanide)gold(I) chloride; water; potassium tetrakis(pentafluorophenyl)borate In methanol at 20℃; for 24h; Reagent/catalyst; | 99% |
With methanol; [Co((dimethylglyoximate)BF2)2•2H2O] at 65℃; for 2.5h; Sealed tube; Neutral conditions; regioselective reaction; | 98% |
With silver hexafluoroantimonate; SPGS-550-M; NOK; C35H47O3P*Au(1+)*Cl(1-); trifluoroacetic acid In water; toluene at 20℃; for 24h; Green chemistry; | 90% |
2-methyl-5,6-dihydro-4H-pyran-3-carboxylic acid methyl ester
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With hydrogenchloride at 50℃; for 3h; | 93% |
1-methylcyclopentyl hypochlorite
6-chloro-2-hexanone
Conditions | Yield |
---|---|
In tetrachloromethane at 70℃; for 6h; Irradiation; | 90% |
at 40℃; |
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With hydrogenchloride In tetrahydrofuran for 0.5h; Heating; | 85% |
N'-[5-Chloro-1-methyl-pent-(Z)-ylidene]-N,N-dimethyl-hydrazine
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With water; copper dichloride In tetrahydrofuran; phosphoric acid | 84% |
With boron trifluoride diethyl etherate In water; acetone | 64% |
5-(1-Amino-5-chloro-pentylidene)-2,2-dimethyl-[1,3]dioxane-4,6-dione
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With hydrogenchloride Heating; | 73% |
Conditions | Yield |
---|---|
With pyridine; lead(IV) acetate; lithium chloride In benzene at 80℃; for 5h; | A 15% B 70% |
Methyltriphenylphosphonium bromide
4-Chloro-N,O-dimethylbutyric acid amide
6-chloro-2-hexanone
Conditions | Yield |
---|---|
Stage #1: Methyltriphenylphosphonium bromide With n-butyllithium In tetrahydrofuran; hexane at -15℃; Stage #2: 4-Chloro-N,O-dimethylbutyric acid amide In tetrahydrofuran; hexane at -78 - 20℃; Wittig reaction; Stage #3: With hydrogenchloride In tetrahydrofuran; diethyl ether; hexane at 20℃; | 68% |
6-chloro-2-hexanol
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With C44H66O8P4Pd2; methyl vinyl ketone In water; toluene at 105℃; for 16h; Inert atmosphere; chemoselective reaction; | 65% |
With pyridinium chlorochromate |
Conditions | Yield |
---|---|
With dichloro bis(acetonitrile) palladium(II); oxygen; 2-Methyl-1,4-benzoquinone; copper(l) chloride; tert-butyl alcohol at 40℃; under 760.051 Torr; for 3h; | A 8 %Spectr. B 60% |
Conditions | Yield |
---|---|
With dichloro bis(acetonitrile) palladium(II); 1-hydroxytetraphenyl-cyclopentadienyl(tetraphenyl-2,4-cyclopentadien-1-one)-μ-hydrotetracarbonyldiruthenium(II); water; p-benzoquinone In methanol; isopropyl alcohol at 85℃; for 48h; Inert atmosphere; Glovebox; regioselective reaction; | A 40% B 9 %Spectr. |
6-hydroxy-2-hexanone
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With hydrogenchloride; water |
1-methyl-cyclopentyl hydroperoxide
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With hydrogenchloride; iron(II) sulfate In water |
N-isopropyliden-cyclohexyl amine
1,3-chlorobromopropane
6-chloro-2-hexanone
Conditions | Yield |
---|---|
(i) LiNEt2, THF, (ii) /BRN= 605278/, (iii) aq. HCl; Multistep reaction; | |
With n-butyllithium 1.) THF; Yield given. Multistep reaction; |
1,3-Dioxolan-2-buttersaeure-ethylester
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With hydrogenchloride; lithium aluminium tetrahydride 1) ether, 4 h, room temp.; 30 min., reflux; 2) 2 h, reflux; Yield given. Multistep reaction; |
5-chloro-2-(1-methylethenyl)pentanoic acid
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With pyridine; dimethylsulfide; ozone 1.) dichloromethane, -70 deg C, 2.) dichloromethane, room temperature, 15 h; Yield given. Multistep reaction; |
5-chloro-2-(1-methylethenyl)pentanoic acid
A
6-chloro-2-hexanone
B
6-chloro-3-methylene-2-hexanone
Conditions | Yield |
---|---|
With ozone; triethylamine 1.) dichloromethane, -70 deg C, 2.) dichloromethane, room temperature; Yield given. Multistep reaction. Yields of byproduct given; |
6-chloro-2-(1-methylethenyl)hexanoic acid
A
6-chloro-2-hexanone
B
7-chloroheptan-2-one
Conditions | Yield |
---|---|
With pyridine; dimethylsulfide; ozone 1.) dichloromethane, -70 deg C, 2.) dichloromethane, room temperature, 15 h; Yield given. Multistep reaction. Yields of byproduct given; |
A
6-chloro-2-hexanone
B
8-chloro-octan-2-one
Conditions | Yield |
---|---|
With pyridine; dimethylsulfide; ozone 1.) dichloromethane, -70 deg C, 2.) dichloromethane, room temperature, 15 h; Yield given. Multistep reaction. Yields of byproduct given; |
5-Chlorovaleroyl chloride
6-chloro-2-hexanone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: 70 percent / tetrahydrofuran / -78 °C 2.1: n-BuLi / tetrahydrofuran; hexane / -15 °C 2.2: tetrahydrofuran; hexane / -78 - 20 °C 2.3: 68 percent / aq. HCl / tetrahydrofuran; hexane; diethyl ether / 20 °C View Scheme |
5-chloro-pentanal
6-chloro-2-hexanone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: pyridinium chlorochromate View Scheme |
Conditions | Yield |
---|---|
Stage #1: propylamine; 6-chloro-2-hexanone; calcium carbide With copper(l) iodide; triethylamine In water; acetonitrile at 60℃; for 24h; Stage #2: In water; acetonitrile for 2h; Reagent/catalyst; Solvent; | 99% |
6-chloro-2-hexanone
1-iodo-5-hexanone
Conditions | Yield |
---|---|
With sodium iodide In acetone at 60℃; for 12h; Sealed tube; | 97% |
With sodium iodide In acetone at 60℃; | 87% |
With sodium iodide In acetone | |
With sodium iodide In acetone Heating; |
N-Methylpyrrole
6-chloro-2-hexanone
3-(5-chloro-1-methylpentyl)-1-methyl-1H-pyrrole
Conditions | Yield |
---|---|
With triethylsilane; indium(III) tris[bis(trifluoromethanesulfonyl)amide] In 1,4-dioxane at 85℃; for 5h; Schlenk technique; Inert atmosphere; regioselective reaction; | 97% |
With triethylsilane; bis(trifluoromethanesulfonyl)amide In 1,4-dioxane at 100℃; for 10h; Schlenk technique; Inert atmosphere; regioselective reaction; | 86% |
Conditions | Yield |
---|---|
Stage #1: 6-chloro-2-hexanone; calcium carbide; phenethylamine With copper(l) iodide; triethylamine In water; acetonitrile at 60℃; for 24h; Stage #2: In water; acetonitrile for 2h; Reagent/catalyst; | 96% |
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With iodine; 1-n-butyl-3-methylimidazolim bromide at 80℃; for 15h; Reagent/catalyst; Temperature; Ionic liquid; Green chemistry; chemoselective reaction; | 93% |
6-chloro-2-hexanone
6-azido-2-hexanone
Conditions | Yield |
---|---|
With sodium azide; sodium iodide In dimethyl sulfoxide at 55℃; for 18h; | 92% |
With sodium azide; sodium iodide In N,N-dimethyl-formamide at 80℃; for 5h; Inert atmosphere; | 81% |
With sodium azide; sodium iodide In N,N-dimethyl-formamide at 80℃; | 67% |
With sodium azide; sodium iodide In N,N-dimethyl-formamide at 80℃; for 2h; Inert atmosphere; | 59% |
Conditions | Yield |
---|---|
With acetic acid for 4h; Reflux; | 92% |
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With iodine; 1-n-butyl-3-methylimidazolim bromide at 80℃; for 14h; Ionic liquid; Green chemistry; chemoselective reaction; | 92% |
6-chloro-2-hexanone
7-Ethyl-3,8-dimethyl-3,7-dihydro-purine-2,6-dione
Conditions | Yield |
---|---|
With sodium ethanolate In N,N-dimethyl-formamide at 125℃; for 4h; | 91% |
phthalimide
6-chloro-2-hexanone
2-(5-oxohexyl)-1H-isoindole-1,3(2H)-dione
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 100℃; for 12h; | 91% |
With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 100℃; for 18h; | 73.2% |
6-chloro-2-hexanone
2-amino-N'-phenylbenzohydrazide
Conditions | Yield |
---|---|
With iodine; 1-n-butyl-3-methylimidazolim bromide at 80℃; for 15h; Ionic liquid; Green chemistry; chemoselective reaction; | 91% |
6-chloro-2-hexanone
C13H12ClN3O
Conditions | Yield |
---|---|
With iodine; 1-n-butyl-3-methylimidazolim bromide at 80℃; for 13h; Ionic liquid; Green chemistry; chemoselective reaction; | 91% |
Conditions | Yield |
---|---|
With manganese; TiCpCl2 In tetrahydrofuran at 20℃; for 2h; Inert atmosphere; | 91% |
6-chloro-2-hexanone
7-benzyl-3-methylxanthine
Conditions | Yield |
---|---|
90.4% |
6-chloro-2-hexanone
2-amino-N-(4-methoxyphenyl)benzamide
Conditions | Yield |
---|---|
With iodine at 80℃; for 8h; Ionic liquid; | 90% |
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With iodine; 1-n-butyl-3-methylimidazolim bromide at 80℃; for 11h; Ionic liquid; Green chemistry; chemoselective reaction; | 90% |
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With iodine at 80℃; for 9h; Ionic liquid; | 90% |
6-chloro-2-hexanone
3-Ethyl-7,8-dimethyl-3,7-dihydro-purine-2,6-dione
Conditions | Yield |
---|---|
With sodium ethanolate In N,N-dimethyl-formamide at 125℃; for 4h; | 89% |
6-chloro-2-hexanone
2-amino-N-(p-methoxybenzyl)benzamide
Conditions | Yield |
---|---|
With iodine at 80℃; for 8h; Ionic liquid; | 89% |
6-chloro-2-hexanone
2-Amino-5-chlor-N2-phenyl-benzoesaeure-hydrazid
Conditions | Yield |
---|---|
With iodine; 1-n-butyl-3-methylimidazolim bromide at 80℃; for 11h; Ionic liquid; Green chemistry; chemoselective reaction; | 89% |
6-chloro-2-hexanone
2-(aminophenyl)benzimidazole
Conditions | Yield |
---|---|
With iodine at 80℃; for 11h; Ionic liquid; | 89% |
Conditions | Yield |
---|---|
With copper(I) oxide In acetonitrile at 90℃; for 24h; Inert atmosphere; | 88% |
6-chloro-2-hexanone
2-amino-N-[2-(4-methoxyphenyl)ethyl]benzamide
Conditions | Yield |
---|---|
With iodine at 80℃; for 8h; Ionic liquid; | 87% |
2-methyl-1H-indole
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With indium(III) tris[bis(trifluoromethanesulfonyl)amide]; methyldiphenylsilane In 1,4-dioxane at 50℃; for 24h; Inert atmosphere; Schlenk technique; | 87% |
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With iodine; 1-n-butyl-3-methylimidazolim bromide at 80℃; for 10h; Ionic liquid; Green chemistry; chemoselective reaction; | 87% |
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