CAS No.78-95-5,Chloroacetone Suppliers

Hunan Russell Chemicals Technology Co.,Ltd

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Chloroacetone, 95%, stabilized 78-95-5

Cas:78-95-5

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Pure Chemistry Scientific Inc.

78-95-5 Application:Chloroacetone

Chloroacetone

Cas:78-95-5

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Synthetic route

: 67-64-1
acetone

: 78-95-5
chloroacetone

Conditions

Conditions	Yield
With chlorine; calcium carbonate In water at 110℃; Reagent/catalyst; Temperature;	95.6%
With methanol; sulfuryl dichloride In dichloromethane	85%
With sulfuryl dichloride

: 35952-61-5
(C4H9)3SnOCH(CH2Cl)2

A: 1461-22-9
tributyltin chloride

B: 78-95-5
chloroacetone

C: 106-89-8
epichlorohydrin

Conditions

Conditions	Yield
63% decompn. at 210°C (1 h);	A n/a B 5% C 95%

...Expand

: 67-64-1
acetone

A: 513-88-2
1,1-Dichloroacetone

B: 78-95-5
chloroacetone

Conditions

Conditions	Yield
With trichloroisocyanuric acid; boron trifluoride diethyl etherate In acetic acid for 1h; Heating; Yields of byproduct given;	A n/a B 88%
With water; chlorine; calcium carbonate

: 4755-81-1
methyl 2-chloroacetoacetate

: 78-95-5
chloroacetone

Conditions

Conditions	Yield
With sulfuric acid for 3h; Heating;	85%

: 96-23-1
1,3-Dichloro-2-propanol

A: 78-95-5
chloroacetone

B: 106-89-8
epichlorohydrin

Conditions

Conditions	Yield
With HT4-c823 In water at 149.84℃; under 750.075 Torr; for 0.5h; Catalytic behavior; Reagent/catalyst; Temperature; Flow reactor; chemoselective reaction;	A 18.9% B 80.5%

: 2684-62-0
diazoacetone

A: 78-95-5
chloroacetone

B: 177084-70-7
2-diazo-3-oxobutanal

Conditions

Conditions	Yield
With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane for 1h; Ambient temperature;	A 50% B 14%

: 2684-62-0
diazoacetone

: 68-12-2, 33513-42-7
N,N-dimethyl-formamide

A: 78-95-5
chloroacetone

B: 177084-70-7
2-diazo-3-oxobutanal

Conditions

Conditions	Yield
With oxalyl dichloride In dichloromethane for 1h; Ambient temperature;	A 50% B 14%

...Expand

: 2684-62-0
diazoacetone

A: 4,5-dimethylfuran-3(2H)-one

B: 116-09-6
hydroxy-2-propanone

C: 78-95-5
chloroacetone

D: 76089-31-1
1,1'-oxydi(propan-2-one)

Conditions

Conditions	Yield
With hydrogenchloride; gallium(III) trichloride; water In dichloromethane at 20℃; for 0.0833333h;	A 34% B 8% C 20% D 31%

...Expand

: 173063-66-6
cis/trans-3,5-Bis-(chloromethyl)-3-fluoro-5-methyl-1,2,4-trioxolane

A: 78-95-5
chloroacetone

B: 79-04-9
chloroacetyl chloride

C: Chloro-acetic acid 1,2-dichloro-1-methyl-ethyl ester

Conditions

Conditions	Yield
With triphenylphosphine In chloroform-d1	A 28 % Spectr. B 23 % Spectr. C 33%

...Expand

: 115290-60-3
{Pd2(μ-H)(COCH3)2(μ-dppm)2}BPh4

: 98194-67-3
Pd2(CH3)2(Cl)2(μdppm)2

B: 75-07-0
acetaldehyde

C: 78-95-5
chloroacetone

Conditions

Conditions	Yield
In dichloromethane warming of {Pd2(μ-H)(COCH3)2(dppm)2}BPh4 in CH2Cl2 (23°C, 24 h);	A 32% B n/a C n/a

...Expand

: 674-82-8
4-methyleneoxetan-2-one

: 78-95-5
chloroacetone

Conditions

Conditions	Yield
With chlorine at 0 - 10℃; Kochen des Reaktionsprodukts mit Wasser;

: 78-88-6
2,3-Dichloroprop-1-ene

: 78-95-5
chloroacetone

Conditions

Conditions	Yield
With sulfuric acid Destillieren der Loesung mit Wasser;

: 2684-62-0
diazoacetone

: 78-95-5
chloroacetone

Conditions

Conditions	Yield
With hydrogenchloride; diethyl ether
Stage #1: diazoacetone With ethylaluminum dichloride In hexane; dichloromethane at 20℃; for 0.0166667h; Stage #2: With methanol In hexane; dichloromethane

: 463-49-0
1,2-propanediene

: 78-95-5
chloroacetone

Conditions

Conditions	Yield
With water; chlorine

: 67-66-3
chloroform

: 29843-58-1
1,4-dichloro-2-methyl-2-butene

A: 107-20-0
2-chloroethanal

B: 78-95-5
chloroacetone

Conditions

Conditions	Yield
beim Ozonisierung und Behandeln des Ozonids mit Wasser bei 75-80grad;

...Expand

: 52842-49-6
(E)-1,3-dichloro-2-methyl-2-butene

A: 64-19-7
acetic acid

B: 78-95-5
chloroacetone

Conditions

Conditions	Yield
bei der Ozonspaltung;

: 33401-05-7
β-chloro-α-hydroxy-isobutyronitrile

A: 74-90-8
hydrogen cyanide

B: 78-95-5
chloroacetone

Conditions

Conditions	Yield
beim Destillieren unter gewoehnlichem Druck;

: 624-85-1
ethyl hypochlorite

: 67-64-1
acetone

: 78-95-5
chloroacetone

: 106471-36-7
bis(2-chloroethyl)selenium dichloride

: 67-64-1
acetone

: 78-95-5
chloroacetone

: 116008-96-9
bis(2-bromoethyl)selenium dichloride

: 67-64-1
acetone

: 78-95-5
chloroacetone

: 3135-74-8
chlorourea

: 67-64-1
acetone

: 78-95-5
chloroacetone

Conditions

Conditions	Yield
With water

: 538-74-9
dibenzyl sulfide

: 67-64-1
acetone

: 1821-34-7
N-chlorobenzamide

A: N-benzoyl-S,S-dibenzyl-sulfimide

B: 78-95-5
chloroacetone

Conditions

Conditions	Yield
at -20℃;

...Expand

: 590-21-6
propenyl chloride

: 78-95-5
chloroacetone

Conditions

Conditions	Yield
With N-oxo-N-nitrosoamine at 280℃; under 367754 Torr;

: 127-00-4
1-Chloro-2-propanol

: 78-95-5
chloroacetone

Conditions

Conditions	Yield
With chromic acid
With ruthenium(IV) oxide; sodium chloride In water; ethyl acetate electrooxidation;
With sodium hydroxide; N-bromoacetamide In water at 24.9℃; Mechanism; Kinetics; Thermodynamic data; var. of temp. (Tab. VI); ΔH(excit.), ΔS(excit.), ΔF(excit.);

: 75-56-9, 16033-71-9
methyloxirane

: 78-95-5
chloroacetone

Conditions

Conditions	Yield
With chlorine at 0℃;

: 186581-53-3, 908094-01-9
diazomethane

: 75-36-5
acetyl chloride

: 78-95-5
chloroacetone

Conditions

Conditions	Yield
With hydrogenchloride 1.) ether, 2 h, -20 to 0 deg C, 2.) -20 deg C to room temp.; Multistep reaction;

: 5950-21-0
2-chloro-1,2-epoxypropane

: 78-95-5
chloroacetone

Conditions

Conditions	Yield
for 48h;

: 96-23-1
1,3-Dichloro-2-propanol

A: 616-23-9
2,3-Dichloro-1-propanol

B: 96-18-4
1,2,3-trichloropropane

C: 23916-48-5
1-chloro-3-(2-chloro-1-chloromethyl-ethoxy)-propan-2-ol

D: 78-95-5
chloroacetone

Conditions

Conditions	Yield
at 180℃; Product distribution; also in the presence of 1.5 percent HCl or 5percent epichlorhydrin;

...Expand

: 108-96-3
4-pyridone

: 78-95-5
chloroacetone

: 153075-85-5
1-(2-oxopropyl)-4-pyridone

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 60℃; for 4h;	100%

: 111-88-6
Octanethiol

: 78-95-5
chloroacetone

: 20233-08-3
3-Octylthiopropan-2-one

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran at 20℃; for 1h;	100%
With potassium carbonate In tetrahydrofuran

: 2687-43-6
O-benzylhydoxylamine hydrochloride

: 78-95-5
chloroacetone

: 83200-26-4
1-chloropropan-2-one O-benzyloxime

Conditions

Conditions	Yield
With sodium hydrogencarbonate In water at 20℃; for 5h;	100%
With sodium hydroxide In methanol 2.) room temp., 5 h;	91%

: 123979-29-3
2,6-dimethyl-1,5-dihydroxynaphthalene

: 78-95-5
chloroacetone

: 137517-19-2
2,6-Dimethyl-1,5-bis(2-oxopropoxy)naphthalene

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide Ambient temperature;	100%

: 137517-25-0
2,6-Dipropyl-1,5-naphthalenediol

: 78-95-5
chloroacetone

: 137517-22-7
2,6-Dipropyl-1,5-bis(2-oxopropoxy)naphthalene

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide Ambient temperature;	100%

: 132483-78-4
Diethyl 2-methyl-2-(4-thiocarbamoylphenyl)malonate

: 78-95-5
chloroacetone

: 138569-11-6
Diethyl 2-methyl-2-<4-(4-methylthiozol-2-yl)phenyl>malonate

Conditions

Conditions	Yield
In benzene for 3.25h; Heating;	100%

: 78-95-5
chloroacetone

: 18156-75-7
1-trimethylsilylpyrazole

: (chloro-1' trimethylsiloxy-2' isopropyl)-1 pyrazole

Conditions

Conditions	Yield
at 80℃; for 1h;	100%

: 78-95-5
chloroacetone

: 18293-54-4
1-trimethylsilyl-1,2,4-triazole

: (chloro-1' trimethylsiloxy-2' isopropyl)-1 triazole-1,2,4

Conditions

Conditions	Yield
at 100℃; for 1h;	100%

: 78-95-5
chloroacetone

: 43183-36-4
1-(trimethylsilyl)-1H-benzotriazole

: (chloro-1' trimethylsiloxy-2' isopropyl)-1 benzotriazole

Conditions

Conditions	Yield
at 100℃; for 1h;	100%

: 78-95-5
chloroacetone

: 15264-63-8
5-(4-pyridinyl)-1,3,4-oxadiazole-2-thiol

: 81555-96-6
1-(5-Pyridin-4-yl-[1,3,4]oxadiazol-2-ylsulfanyl)-propan-2-one

Conditions

Conditions	Yield
With sodium hydroxide for 12h; Ambient temperature;	100%

: 110766-90-0
8-Chloro-2-methyl-2,3-dihydro-5H-benzo[b][1,4]thiazepin-4-one

: 78-95-5
chloroacetone

: 8-Chloro-2-methyl-5-(2-oxo-propyl)-2,3-dihydro-5H-benzo[b][1,4]thiazepin-4-one

Conditions

Conditions	Yield
With potassium hydroxide; tetrabutylammomium bromide In tetrahydrofuran Ambient temperature;	100%

: 78-95-5
chloroacetone

: 216776-76-0
6-Fluoro-4-methyl-2-phenyl-thieno[2,3-d]pyrimidin-5-ylamine

: 115073-27-3
6-acetyl-5-amino-4-methyl-2-phenylthieno[2,3-d]pyrimidine

Conditions

Conditions	Yield
With potassium carbonate	100%

: 149-30-4
2-Mercaptobenzothiazole

: 78-95-5
chloroacetone

: 2-acetonylthiobenzimidazole hydrochloride

Conditions

Conditions	Yield
at 60℃; for 12h; Solid phase reaction; substitution;	100%

: 78-95-5
chloroacetone

: 239131-42-1
5-(2-chlorophenyl)-3-mercapto-2-cyclohexen-1-one

: 239131-43-2
5-(2-chlorophenyl)-3-[(2-oxopropyl)thio]-2-cyclohexen-1-one

Conditions

Conditions	Yield
With sodium ethanolate In ethanol at 20℃; for 5h;	100%
With sodium ethanolate In ethanol at 20℃; for 5h;

: 1898-85-7
dibenzo[b,f]thiepin-10(11H)-one

: 78-95-5
chloroacetone

: 1-(dibenzo[b,f]thiepin-10-yloxy)-propan-2-one

Conditions

Conditions	Yield
With sodium hydride In dimethyl sulfoxide	100%
With sodium hydride In dimethyl sulfoxide at 20℃;	23%

: 496-69-5
2-bromo-4-fluoro-phenol

: 78-95-5
chloroacetone

: 286836-12-2
1-(2-bromo-4-fluorophenoxy)propan-2-one

Conditions

Conditions	Yield
With potassium carbonate; potassium iodide In tetrahydrofuran for 4h; Heating / reflux;	100%
With potassium carbonate; potassium iodide In tetrahydrofuran for 4h; Heating / reflux;	100%
With potassium carbonate In N,N-dimethyl-formamide at 0 - 20℃;	59%
With potassium carbonate; potassium iodide In acetone at 55℃; for 2h;
With potassium iodide; potassium carbonate In tetrahydrofuran; ethyl acetate	2.7 gm (100%)

: 39835-11-5
2-hydroxy-4 methoxybenzonitrile

: 78-95-5
chloroacetone

: 869789-23-1
C11H11NO3

Conditions

Conditions	Yield
With potassium carbonate; potassium iodide In acetone at 0 - 20℃; for 1h; Heating / reflux;	100%

: 872707-11-4
N-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)pyridin-2-yl]thiourea

: 78-95-5
chloroacetone

: 872707-12-5
{2-[(4-methyl-1,3-thiazol-2-yl)amino]pyridin-4-yl}methanol

Conditions

Conditions	Yield
In ethanol for 16h; Heating / reflux;	100%
In ethanol for 16h; Heating / reflux;	100%
In ethanol for 16h; Heating / reflux; Under nitrogen;	100%

: 1059686-59-7
2-Cyclopropylamino-4,6-difluoro-benzoic acid

: 78-95-5
chloroacetone

: 1059686-60-0
2-Cyclopropylamino-4,6-difluoro-benzoic acid 2-oxo-propyl ester

Conditions

Conditions	Yield
Stage #1: 2-Cyclopropylamino-4,6-difluoro-benzoic acid With potassium carbonate In N,N-dimethyl-formamide at 90℃; for 1h; Stage #2: chloroacetone In N,N-dimethyl-formamide at 20 - 55℃; for 1.5h;	100%

: 953045-29-9
1-(5-bromo-3-(phenylthio)pyridin-2-yl)thiourea

: 78-95-5
chloroacetone

: 953040-73-8
N-(5-bromo-3-(phenylthio)pyridin-2-yl)-4-methylthiazol-2-amine

Conditions

Conditions	Yield
With triethylamine In ethanol at 70℃; for 6h;	100%

: 1189115-86-3
tert-butyl (S)-1-amino-3-(1H-indol-3-yl)-1-thioxopropan-2-yl carbamate

: 78-95-5
chloroacetone

: 1189115-87-4
tert-butyl [(S)-1-(4-hydroxy-4-methyl-4,5-dihydro-thiazol-2-yl)-2-(1H-indol-3-yl)-ethyl]-carbamate

Conditions

Conditions	Yield
With potassium hydrogencarbonate In 1,2-dimethoxyethane at 45 - 70℃;	100%

: 1186033-44-2
C9H9ClOS

: 78-95-5
chloroacetone

: 66490-34-4
1-(4-chloro-1H-benzo[b]thiophen-2-yl)ethanone

Conditions

Conditions	Yield
With calcium oxide In acetone at 59℃;	100%
With calcium oxide for 3h; Reflux;

: 53606-33-0
2-(ethylsulfanyl)benzenecarbaldehyde

: 78-95-5
chloroacetone

: 22720-75-8
2-acetyl benzo[b]thiophene

Conditions

Conditions	Yield
With calcium oxide In acetone at 59℃;	100%
With calcium oxide for 3h; Reflux;

: 288-88-0
1,2,4-Triazole

: 78-95-5
chloroacetone

: 64882-52-6
1-(1H-1,2,4-triazol-1-yl)propan-2-one

Conditions

Conditions	Yield
With potassium carbonate In acetone at 60℃; for 20h;	100%
With sodium hydrogencarbonate In toluene at 110 - 120℃; for 3h; Inert atmosphere;	22.2%

: coenzyme A disodium salt

: 78-95-5
chloroacetone

: 75179-85-0
acetonyl-CoA

Conditions

Conditions	Yield
With N,N-dimethyl-formamide In water at 0 - 5℃; Inert atmosphere;	100%

: 78-95-5
chloroacetone

: 188115-27-7
(S)-11-thioxo-2,3,11,11a-tetrahydro-1H-benzo[e]-pyrrolo[1,2-a][1,4]diazepin-5(10H)-one

: 1271450-06-6
C15H16N2O2S

Conditions

Conditions	Yield
Stage #1: (S)-11-thioxo-2,3,11,11a-tetrahydro-1H-benzo[e]-pyrrolo[1,2-a][1,4]diazepin-5(10H)-one With sodium hydride In dimethyl sulfoxide at 20℃; for 0.5h; Inert atmosphere; Stage #2: chloroacetone In dimethyl sulfoxide at 20℃; for 0.666667h; Inert atmosphere;	100%

: 1152617-24-7
2-amino-3-chloro-4-iodopyridine

: 78-95-5
chloroacetone

: 1416551-60-4
8-chloro-7-iodo-2-methylimidazo[1,2-a]pyridine

Conditions

Conditions	Yield
In ethanol at 65℃;	100%

: 576-23-8
2,3-dimethylbromobenzene

: 78-95-5
chloroacetone

: 42432-45-1
2-(2,3-dimethylphenyl)-2-methyloxirane

Conditions

Conditions	Yield
Stage #1: 2,3-dimethylbromobenzene With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.5h; Stage #2: chloroacetone In tetrahydrofuran; hexane; toluene at -78 - 20℃; for 1.33333h; Product distribution / selectivity;	100%
Stage #1: 2,3-dimethylbromobenzene With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.5h; Stage #2: chloroacetone In tetrahydrofuran; hexane; toluene at -78 - 20℃; Product distribution / selectivity;	100%

: 59108-90-6
1H-indole-3-carbothioamide

: 78-95-5
chloroacetone

: 93588-10-4
4-methyl-2-(3-indolyl)thiazole

Conditions

Conditions	Yield
In ethanol at 80℃; for 1.5h; Reflux;	100%

: C21H22N4O

: 78-95-5
chloroacetone

: C24H26N4O2

Conditions

Conditions	Yield
With potassium carbonate In dichloromethane; acetonitrile at 20℃; for 8h; Reflux;	100%
With potassium carbonate In dichloromethane; acetonitrile for 8h; Reflux;	100%
With potassium carbonate In dichloromethane; acetonitrile for 8h; Reflux;

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