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Cas:534-07-6
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiryConditions | Yield |
---|---|
With potassium chloride In water at 20 - 60℃; for 0.333333h; | 98% |
bromo-3-chloro-propanone
3-mercaptopropionitrile
B
1,3-Dichloroacetone
Conditions | Yield |
---|---|
A 94% B n/a |
Conditions | Yield |
---|---|
With periodic acid In acetonitrile at 20℃; for 3h; Reagent/catalyst; Solvent; Temperature; | 80% |
With chromic acid | |
With chromium(III) oxide; sulfuric acid |
Conditions | Yield |
---|---|
With methyllithium; lithium bromide In tetrahydrofuran; diethyl ether at -78℃; for 0.333333h; | 60% |
Yield given. Multistep reaction; |
2,4-Dichlor-3-aminocrotonsaeurenitril
1,3-Dichloroacetone
Conditions | Yield |
---|---|
With hydrogenchloride for 72h; | 58% |
(Z)-1,3-Dichlor-2,4,4-trimorpholino-1,3-butadien-1-carbonitril
1,3-Dichloroacetone
Conditions | Yield |
---|---|
With hydrogenchloride at 60 - 70℃; for 10h; 2) Et2O, heating; | 15% |
diazomethane
phosgene
diethyl ether
1,3-Dichloroacetone
Conditions | Yield |
---|---|
With diethyl ether |
Conditions | Yield |
---|---|
With hypochloric acid |
Conditions | Yield |
---|---|
beim partielle Disproportionierung; |
Conditions | Yield |
---|---|
With hypochloric acid |
Conditions | Yield |
---|---|
With chlorine at -20℃; im Licht; |
Conditions | Yield |
---|---|
With silver(I) chloride |
1-chloro-3-diazopropan-2-one
1,3-Dichloroacetone
Conditions | Yield |
---|---|
With hydrogenchloride | |
With hydrogenchloride In diethyl ether for 4h; Heating; Yield given; |
Conditions | Yield |
---|---|
With chlorine; nickel dichloride |
Conditions | Yield |
---|---|
With iron(III) chloride at 45℃; bei der Chlorierung; | |
With chlorine In tetrachloromethane Product distribution; 1.) below 40 deg C, 2.) room temperature, 0.5 h; | A 67 % Chromat. B 33 % Chromat. |
With chlorine; acetic acid | |
With hydrogenchloride; chlorine | |
With antimonypentachloride; chlorine |
Conditions | Yield |
---|---|
With disulfur dichloride beim Siedetemperatur; | |
With disulfur dichloride |
Conditions | Yield |
---|---|
In chlorobenzene Heating; |
1,2-propanediene
A
dichloride of 1-chloro-2-propene-2-phosphonic acid
B
dichloride of 2-chloro-2-propene-1-phosphonic acid
C
1,3-Dichloroacetone
Conditions | Yield |
---|---|
With oxygen; phosphorus trichloride Product distribution; |
Conditions | Yield |
---|---|
With ruthenium(IV) oxide; sodium chloride In water; ethyl acetate at 5℃; Product distribution; other organic solvents; | A 1 % Chromat. B 62 % Chromat. |
1,3-dichloro-2,2-propanediol
1,3-Dichloroacetone
Conditions | Yield |
---|---|
With dehydration at 25℃; Rate constant; Equilibrium constant; Thermodynamic data; ΔH(excit.), ΔS(excit.), ΔG(excit.); isotope effects; | |
With water In acetonitrile Equilibrium constant; various temperatures (15-46 deg C), isotope effect; |
Butane-1,4-diol
acetone
A
1,1-Dichloroacetone
C
2,2-Bis(chloromethyl)-1,3-dioxacycloheptane
D
2-dichloromethyl-2-methyl-1,3-dioxepane
E
chloroacetone
F
1,3-Dichloroacetone
Conditions | Yield |
---|---|
With chlorine Product distribution; 1.) 20-50 deg C, 2.) room temperature, 0.5 h; | A n/a B n/a C 28.3 % Chromat. D 13.8 % Chromat. E n/a F n/a |
Butane-1,4-diol
acetone
A
1,1-Dichloroacetone
B
2,2-Bis(chloromethyl)-1,3-dioxacycloheptane
C
2-dichloromethyl-2-methyl-1,3-dioxepane
D
1,3-Dichloroacetone
Conditions | Yield |
---|---|
With chlorine 1) 20-50 deg C; 2) room temp., 0.5 h; Further byproducts given. Yields of byproduct given; | A n/a B 28.3 % Chromat. C n/a D n/a |
acetone
A
1,1-Dichloroacetone
B
chloroacetone
C
1,3-Dichloroacetone
Conditions | Yield |
---|---|
With hydrogenchloride at 23 - 25℃; electrochemical; Yield given. Yields of byproduct given. Title compound not separated from byproducts; | |
With hydrogenchloride at 23 - 25℃; electrochemical; Yield given. Yields of byproduct given; | |
With hydrogenchloride at 22 - 25℃; Product distribution; function of current and concentration; |
1,3-Dichloroacetone
Conditions | Yield |
---|---|
With sulfuric acid |
1,3-Dichloroacetone
Conditions | Yield |
---|---|
With hydrogenchloride |
1,3-Dichloroacetone
hydrazinecarboxylic acid methyl ester
1,3-Dichloroacetone
methyl 2-[2-chloro-1-(chloromethyl)ethylidene]-1-hydrazinecarboxylate
Conditions | Yield |
---|---|
In diethyl ether for 15h; Ambient temperature; | 100% |
In methanol at 23℃; for 4h; | 54% |
for 3h; Ambient temperature; Yield given; | |
In methanol at 23℃; for 4h; |
1,3-Dichloroacetone
(E)-1,3-dichloroacetone O-(3-phenyl-2-propenyl)oxime
Conditions | Yield |
---|---|
In methanol at 40℃; for 2h; | 100% |
1,3-Dichloroacetone
bis-(2-morpholin-4-yl-thiazol-5-yl)-methanone
Conditions | Yield |
---|---|
Stage #1: 1,3-Dichloroacetone; 1-morpholino-3-(morpholinomethylene)thiourea In acetonitrile for 2h; Heating; Stage #2: With triethylamine In acetonitrile | 100% |
1,3-Dichloroacetone
1,3-diazido-propan-2-one
Conditions | Yield |
---|---|
With sodium azide In acetone at 20℃; | 100% |
With sodium azide In acetone at 20℃; for 12h; | 96% |
With sodium azide In acetone at 20℃; for 12h; | 96% |
2-N-piperidino-5-methyl-1,3-dithiolium-4-thiolate
1,3-Dichloroacetone
Conditions | Yield |
---|---|
In acetone | 100% |
Conditions | Yield |
---|---|
With sodium methylate In ethanol for 1.5h; Heating; | 100% |
Conditions | Yield |
---|---|
In acetone at 20℃; for 72h; | 100% |
Conditions | Yield |
---|---|
In ethanol for 3h; Heating / reflux; | 100% |
1,3-Dichloroacetone
4-(tert-butoxycarbonyl)piperazine-1-thiocarboxamide
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In ethyl acetate; 1,2-dichloro-ethane | 100% |
naphthalene-2-carbothioamide
1,3-Dichloroacetone
4-(chloromethyl)-2-(naphthalen-6-yl)thiazole
Conditions | Yield |
---|---|
In ethanol Heating; | 100% |
6-fluoronaphthalene-2-carbothioamide
1,3-Dichloroacetone
4-(chloromethyl)-2-(2-fluoronaphthalen-6-yl)thiazole
Conditions | Yield |
---|---|
In ethanol Heating; | 100% |
1,3-Dichloroacetone
triethyl phosphite
3-chloro-2-<(diethoxyphosphoryl)oxy>-1-propene
Conditions | Yield |
---|---|
at 100℃; | 99% |
In dichloromethane for 166h; Ambient temperature; | 98% |
at 60 - 100℃; for 3h; | 98.9% |
at 50℃; |
1,3-Dichloroacetone
1,3-dichloroacetone oxime
Conditions | Yield |
---|---|
With sulfuric acid; hydroxylamine hydrochloride In ethanol at 20℃; for 2h; Inert atmosphere; | 99% |
With hydroxylamine |
Conditions | Yield |
---|---|
In benzene for 48h; Heating; | 99% |
triethylsilane
1,3-Dichloroacetone
((1,3-dichloropropan-2-yl)oxy)triethylsilane
Conditions | Yield |
---|---|
Stage #1: 1,3-Dichloroacetone With C8H10BiCl2N; C4H6AgN2(1+)*C24H12BCl8(1-) In dichloromethane-d2 at 25℃; Stage #2: triethylsilane In dichloromethane at 25℃; | 99% |
With C24H36AlN2O2(1+)*C24H12BCl8(1-) In benzene-d6 for 15h; Inert atmosphere; Schlenk technique; Glovebox; | 98 %Spectr. |
Conditions | Yield |
---|---|
In acetonitrile at 80℃; Inert atmosphere; | 99% |
1,3-Dichloroacetone
benzenecarbothioamide
2-phenyl-4-chloromethylthiazole
Conditions | Yield |
---|---|
In ethanol for 4h; Reflux; | 98% |
In ethanol for 2h; Reflux; | 90% |
Stage #1: 1,3-Dichloroacetone; benzenecarbothioamide In acetone Inert atmosphere; Reflux; Stage #2: With sulfuric acid for 0.5h; Inert atmosphere; | 85% |
1,3-Dichloroacetone
triphenylphosphine
(3-chloro-2-oxopropyl)triphenylphosphonium chloride
Conditions | Yield |
---|---|
In tetrahydrofuran for 24h; Reflux; | 98% |
In benzene at 20℃; for 6h; | 98% |
In tetrahydrofuran at 70℃; for 5h; | 97% |
O-benzylhydoxylamine hydrochloride
1,3-Dichloroacetone
1,3-dichloro-2-propanone O-benzyloxime
Conditions | Yield |
---|---|
In ethanol Ambient temperature; | 98% |
In ethanol at 20℃; for 24h; | 2.32 g |
thioacetamide
1,3-Dichloroacetone
4-(chloromethyl)-2-methyl-1,3-thiazole
Conditions | Yield |
---|---|
In acetone | 97% |
at 20 - 50℃; for 20h; | 93% |
92.9% |
Potassium benzoate
1,3-Dichloroacetone
1,3-Dibenzoyl-1,3-dihydroxyacetone
Conditions | Yield |
---|---|
5,11,17,23,29,35-Hexa-p-tert-butyl-37,38,39,40,41,42-hexakis-(3,6,9-trioxadecyloxy)calix<6>arene In water; acetonitrile at 65℃; for 6h; | 97% |
With ethanol |
2,2-Dimethyl-1,3-propanediol
1,3-Dichloroacetone
2,2-bis-(chloromethyl)-5,5-dimethyl-1,3-dioxane
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene Heating; | 97% |
With toluene-4-sulfonic acid In benzene for 19h; Heating; | 97% |
With toluene-4-sulfonic acid In benzene for 18h; Heating; | 97% |
4-trifluoromethylbenzthioamide
1,3-Dichloroacetone
4-chloromethyl-2-[4-(trifluoromethyl)phenyl]thiazole
Conditions | Yield |
---|---|
In toluene Reflux; | 97% |
In toluene at 80℃; for 4h; | 62% |
With thionyl chloride; sodium hydrogencarbonate 1.) 1,2-dichloroethane; Multistep reaction; | |
In 1,2-dichloro-ethane at 130 - 140℃; for 5h; Sealed tube; |
1,3-Dichloroacetone
triphenylphosphine
1-chloro-3-(triphenylphosphoranylidene)acetone
Conditions | Yield |
---|---|
Stage #1: 1,3-Dichloroacetone; triphenylphosphine In tetrahydrofuran for 4h; Heating; Stage #2: With sodium carbonate In methanol at 20℃; for 0.5h; | 97% |
Stage #1: 1,3-Dichloroacetone; triphenylphosphine In tetrahydrofuran for 24h; Heating; Stage #2: With sodium hydrogencarbonate In water Further stages.; | 92% |
In tetrahydrofuran for 24h; Heating; | 91% |
Conditions | Yield |
---|---|
In acetone at 20 - 25℃; for 72h; | 97% |
1,3-Dichloroacetone
trimethyl orthoformate
1,3-dichloroacetone dimethyl acetal
Conditions | Yield |
---|---|
With Amberlyst 15 In dichloromethane | 96% |
1,3-Dichloroacetone
o-methoxycarbonyl-α-diazoacetophenone
Conditions | Yield |
---|---|
With copper acetylacetonate In benzene for 1h; Heating; | 96% |
ethyl 2-amino-2-thioxoacetate
1,3-Dichloroacetone
4-(chloromethyl)thiazole-2-carboxylic acid-ethyl ester
Conditions | Yield |
---|---|
In toluene at 110℃; for 2h; | 96% |
In ethanol Heating / reflux; | 37% |
In ethanol for 15h; Heating; | |
In toluene for 2h; Inert atmosphere; Reflux; | |
In toluene Reflux; |
phenyllithium
1,3-Dichloroacetone
1,3-dichloro-2-hydroxy-2-phenylpropane
Conditions | Yield |
---|---|
Stage #1: phenyllithium With cerium(III) chloride In tetrahydrofuran; diethyl ether; cyclohexane at -78℃; for 0.666667h; Stage #2: 1,3-Dichloroacetone In tetrahydrofuran; diethyl ether; cyclohexane at -78℃; for 0.166667h; | 96% |
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