CAS No.105-39-5,Ethyl chloroacetate Suppliers,MSDS download

Jinan Finer Chemical Co., Ltd

Product description: Product name Ethyl chloroacetate CAS number 105-39-5 Assay ≥99.5% Appearance Colorless transparent liquid Capacity 500mt/year Application Pharmaceuticals

Ethyl chloroacetate

Cas:105-39-5

Min.Order:100 Gram

FOB Price: $12.0

Type:Lab/Research institutions

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Suzhou Sinosun Imp.&Exp. Corporation

Chroma(Pt-Co):10Max; Moisture:0.2%Max; Acidity:0.2%Max; Ethyl Dichloroacetate:0.2%Max;Appearance:colorless Liquid

Ethyl chloracetate

Cas:105-39-5

Min.Order:0

Negotiable

Type:Trading Company

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QINGDAO ON-BILLION INDUSTRAIL CO.,LTD

Ethyl chloroacetate is an important intermediate in the synthesis of pharmaceuticals, pesticides and perfumes, and it also be used as industrial solvents. 1. Colorless liquid. 2. The mature Technical support an professional logistic support 3

Ethyl chloracetate

Cas:105-39-5

Min.Order:0 Metric Ton

Negotiable

Type:Trading Company

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Pure Chemistry Scientific Inc.

Ethyl chloroacetate Application:810753

Ethyl chloroacetate

Cas:105-39-5

Min.Order:1 Gram

FOB Price: $500.0

Type:Trading Company

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Synthetic route

: 64-17-5
ethanol

: 79-11-8
chloroacetic acid

: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
With Candida antarctica lipase B at 20℃; for 36h; Enzymatic reaction;	97%
at 105℃; for 3h; Temperature; Molecular sieve;	97.4%
F-4SK (H form) In tetrachloromethane at 80℃; for 5h;	95%

: 79-11-8
chloroacetic acid

: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
With thionyl chloride In ethanol; dichloromethane for 0.583333h; Cooling with ice;	83%

: 623-33-6
glycine ethyl ester hydrochloride

: 79-04-9
chloroacetyl chloride

: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
With sodium hydrogencarbonate In water; toluene at 20℃; for 13h; Cooling with ice;	80%

: 623-73-4
diazoacetic acid ethyl ester

: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
With tertiary butyl chloride; [HB(3,5-(CF3)2Pz)3]Ag(THF)	73%
With hydrogenchloride
With hydrogenchloride; diethyl ether

: 623-81-4
diethyl sulphite

: 79-11-8
chloroacetic acid

: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
sulfuric acid In ethanol Heating;	66%

: 141-97-9
ethyl acetoacetate

: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
With potassium bromate; hydrogenchloride In N,N-dimethyl-formamide at 20℃; for 12h;	63%

: 623-73-4
diazoacetic acid ethyl ester

A: 105-39-5
chloroacetic acid ethyl ester

B: 1520-50-9
but-2-enedioic acid diethyl ester

Conditions

Conditions	Yield
With tertiary butyl chloride; bis(μ2-2,2,2',2'-tetramethyl-1,3-benzene-di(propanoato-O,O'))rhodium-bismuth at 39.84℃; for 2h; Inert atmosphere;	A 46% B n/a

: 623-73-4
diazoacetic acid ethyl ester

: 140-29-4
phenylacetonitrile

A: 74185-57-2
2-benzyl-5-ethoxy-1,3-oxazole

B: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
aluminium trichloride In neat (no solvent) at 25℃;	A 31% B n/a

...Expand

: 7064-36-0
4-chloro-5-methyl-isoxazole

: 64-17-5
ethanol

A: 141-78-6
ethyl acetate

B: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
With pyridine for 5h; Heating;	A n/a B 25%

...Expand

: 623-73-4
diazoacetic acid ethyl ester

: 507-20-0
tertiary butyl chloride

A: 98551-46-3
2-chloro-3,3-dimethyl-butyric acid ethyl ester

B: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
Photolysis;
Irradiation.mit UV-Licht;

...Expand

: 623-73-4
diazoacetic acid ethyl ester

A: 26697-96-1
bis-(ethoxycarbonyl-chloro-chloromercurio-methyl)-mercury

B: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
With mercury dichloride at 0℃;

: 67-56-1
methanol

: 42345-82-4
(E)-1,2-dichloro-1-ethoxy-ethene

A: 96-34-4
methyl chloroacetate

B: 105-39-5
chloroacetic acid ethyl ester

...Expand

: 620-73-5
phenyl chloroacetate

: 64-17-5
ethanol

: 105-39-5
chloroacetic acid ethyl ester

: 620-73-5
phenyl chloroacetate

: 141-52-6
sodium ethanolate

: 105-39-5
chloroacetic acid ethyl ester

: 56-23-5
tetrachloromethane

: 128-09-6
N-chloro-succinimide

: 2678-54-8
ketene diethyl acetal

A: 74-85-1
ethene

B: 105-39-5
chloroacetic acid ethyl ester

...Expand

: 60-29-7
diethyl ether

: 191340-22-4
chloro-acetyl iodide

A: 75-03-6
ethyl iodide

B: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
at 25℃;
at 25℃; bei mehrtaegiger Einw. unter Lichtausschuss; reagiert analog mit Methylbutylaether;

...Expand

: 60-29-7
diethyl ether

: 191340-22-4
chloro-acetyl iodide

: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
at 25℃; unter Ausschluss von Licht;

: 64-17-5
ethanol

: 80944-05-4
1-ethoxy-2,2-dichloro-ethanol

: 151-50-8
potassium cyanide

: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
at 20℃;

...Expand

: 42345-82-4
(E)-1,2-dichloro-1-ethoxy-ethene

: 64-17-5
ethanol

: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
zweckmaessig in Gegenwart von Katalysatoren;

: 64-17-5
ethanol

: 17368-73-9
N-acetyl-2-chloroacetamide

A: 141-78-6
ethyl acetate

B: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
Product distribution; im Verhaeltnis 99:1;

...Expand

: 64-17-5
ethanol

: 15322-68-6
chloroacetyl-propionyl-amine

A: 105-37-3
Ethyl propionate

B: 105-39-5
chloroacetic acid ethyl ester

...Expand

: 64-17-5
ethanol

: 4960-82-1
dichlorodiacetamide

A: 105-39-5
chloroacetic acid ethyl ester

B: 79-07-2
Chloroacetamide

...Expand

: 64-17-5
ethanol

: 7218-27-1
N-(2-chloroethanoyl)benzamide

A: 93-89-0
benzoic acid ethyl ester

B: 105-39-5
chloroacetic acid ethyl ester

...Expand

: 64-17-5
ethanol

: 79628-75-4
3-(2-amino-4-methyl-anilino)-2-chloro-crotonic acid ethyl ester

A: 1792-41-2
2,5-dimethylbenzimidazole

B: 105-39-5
chloroacetic acid ethyl ester

...Expand

: 42345-82-4
(E)-1,2-dichloro-1-ethoxy-ethene

: 123-51-3
i-Amyl alcohol

A: 5326-92-1
3-methylbutyl chloroacetate

B: 105-39-5
chloroacetic acid ethyl ester

...Expand

: 42345-82-4
(E)-1,2-dichloro-1-ethoxy-ethene

: 111-70-6
n-heptan1ol

A: 34589-22-5
heptyl 2-chloroacetate

B: 105-39-5
chloroacetic acid ethyl ester

...Expand

: 80944-05-4
1-ethoxy-2,2-dichloro-ethanol

: 151-50-8
potassium cyanide

: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
With ethanol at 20℃;

: 42345-82-4
(E)-1,2-dichloro-1-ethoxy-ethene

: 110-15-6
succinic acid

A: 108-30-5
succinic acid anhydride

B: 105-39-5
chloroacetic acid ethyl ester

...Expand

: 42345-82-4
(E)-1,2-dichloro-1-ethoxy-ethene

: 89-78-1
menthol

A: 106916-72-7
2-isopropyl-5-methylcyclohexyl chloroethanoate

B: 105-39-5
chloroacetic acid ethyl ester

...Expand

: 42345-82-4
(E)-1,2-dichloro-1-ethoxy-ethene

: 105-39-5
chloroacetic acid ethyl ester

Conditions

Conditions	Yield
With alcohols
With mono-basic organic acids
With oxalic acid

: 95-77-2
3,4-dichlorophenol

: 105-39-5
chloroacetic acid ethyl ester

: 62855-72-5
ethyl 2-(3,4-dichlorophenoxy)acetate

Conditions

Conditions	Yield
With potassium carbonate In acetone at 80℃; for 18h;	100%
With ethanol; sodium ethanolate

: 105-39-5
chloroacetic acid ethyl ester

: 109-94-4
formic acid ethyl ester

: 33142-21-1
ethyl 2-chloro-3-oxopropanoate

Conditions

Conditions	Yield
With sodium ethanolate In tert-butyl methyl ether at 0 - 20℃; Inert atmosphere; Large scale;	100%
With sodium ethanolate In tert-butyl methyl ether at 0 - 20℃; Inert atmosphere; Large scale;	100%
With potassium tert-butylate In tetrahydrofuran at 0 - 20℃; for 16h; Inert atmosphere;	95%

: 105-39-5
chloroacetic acid ethyl ester

: 89124-45-8
acetic acid ethylester sulfonic acid

Conditions

Conditions	Yield
With sodium sulfate In ethanol; water	100%
With potassium sulfite; ethanol

: 1666-13-3
diphenyl diselenide

: 105-39-5
chloroacetic acid ethyl ester

: 51364-94-4
ethyl 2-(phenylselanyl)acetate

Conditions

Conditions	Yield
Stage #1: diphenyl diselenide With sodium tetrahydroborate In ethanol at 0℃; for 0.166667h; Inert atmosphere; Stage #2: chloroacetic acid ethyl ester In ethanol for 1h; Inert atmosphere;	100%
Stage #1: diphenyl diselenide With sodium tetrahydroborate; ethanol at 0 - 25℃; for 1h; Stage #2: chloroacetic acid ethyl ester at 25℃; for 2h;	98%
Stage #1: diphenyl diselenide With sodium tetrahydroborate In ethanol for 0.166667h; Stage #2: chloroacetic acid ethyl ester In ethanol at 50 - 55℃; for 0.75h;	94%

: 105-39-5
chloroacetic acid ethyl ester

: 85666-09-7
E-3-m-hydroxystyrylpyridine

: 79131-36-5
1-Ethoxycarbonylmethyl-4-[(E)-2-(3-hydroxy-phenyl)-vinyl]-pyridinium; chloride

Conditions

Conditions	Yield
In ethanol for 10h; Heating;	100%

: 105-39-5
chloroacetic acid ethyl ester

: 76799-30-9
1-<2,6-bis(benzyloxy)-4-hydroxyphenyl>-3-<3-(benzyloxy)-4-methoxyphenyl>propane

: 76820-12-7
1-<2,6-bis(benzyloxy)-4-(carbethoxymethoxy)phenyl>-3-(3-hydroxy-4-methoxyphenyl)propane

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 40℃; for 22h;	100%

: 105-39-5
chloroacetic acid ethyl ester

: 63240-52-8
2,3',6-tris(benzyloxy)-4-hydroxy-4'-methoxydihydrochalcone

: 76799-27-4
2,3',6-tris(benzyloxy)-4-(carbethoxymethoxy)-4'-methoxydihydrochalcone

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 40 - 65℃; for 19h;	100%

: 105-39-5
chloroacetic acid ethyl ester

: 588679-10-1
ethyl 2-(4-bromo-2-chlorophenoxy)acetate

Conditions

Conditions	Yield
Stage #1: 4-bromo-2-chlorophenol With potassium carbonate In N,N-dimethyl-formamide at 60℃; for 1h; Stage #2: chloroacetic acid ethyl ester In N,N-dimethyl-formamide at 20℃;	100%

: 29799-07-3
4-adamantylphenol

: 105-39-5
chloroacetic acid ethyl ester

: 52804-25-8
(4-adamantyl-1-yl-phenoxy) acetic acid ethyl ester

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide	100%
With potassium carbonate In N,N-dimethyl-formamide at 20℃;	94.6%
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 12h; Inert atmosphere;	94.6%

: 372-20-3
3-fluorophenol

: 105-39-5
chloroacetic acid ethyl ester

: 777-70-8
(3-fluoro-phenoxy)-acetic acid ethyl ester

Conditions

Conditions	Yield
With potassium carbonate In acetone for 24h; Heating / reflux;	100%
With potassium carbonate In acetone for 8h; Reflux;	70%
With potassium carbonate In acetonitrile for 2h; Reflux;

: 105-39-5
chloroacetic acid ethyl ester

: 119-36-8
methyl salicylate

: 22511-42-8
methyl 2-(2-ethoxy-2-oxoethoxy)benzoate

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 30 - 65℃; for 18h;	100%
With potassium carbonate In acetone for 11h; Reflux;	94%
With potassium iodide; potassium carbonate In acetonitrile
With potassium carbonate In N,N-dimethyl-formamide at 65 - 75℃;

: 394-32-1
1-(5-fluoro-2-hydroxyphenyl)ethan-1-one

: 105-39-5
chloroacetic acid ethyl ester

: 34849-57-5
(2-acetyl-4-fluorophenoxy)acetic acid ethyl ester

Conditions

Conditions	Yield
With potassium carbonate In acetone for 16h; Reflux; Inert atmosphere;	100%

: 3964-56-5
4-bromo-2-chlorophenol

: 105-39-5
chloroacetic acid ethyl ester

: 588679-10-1
ethyl 2-(4-bromo-2-chlorophenoxy)acetate

Conditions

Conditions	Yield
Stage #1: 4-bromo-2-chlorophenol; chloroacetic acid ethyl ester With potassium carbonate In N,N-dimethyl-formamide at 60℃; for 1h; Inert atmosphere; Stage #2: chloroacetic acid ethyl ester In N,N-dimethyl-formamide at 20℃;	100%

: 21392-48-3
7-hydroxy-8-methyl-4-phenyl-chromen-2-one

: 105-39-5
chloroacetic acid ethyl ester

: 307547-31-5
ethyl (8-methyl-4-phenyl-2H-1-benzopyran-2-on-7-yloxy)-acetate

Conditions

Conditions	Yield
With potassium carbonate In acetone for 24h; Reflux;	100%
With potassium carbonate In acetone for 6h; Reflux;	96.94%

: 1245623-59-9
5-(5-chloro-2-thienyl)-4-(2-methoxyethyl)-2,4-dihydro-3H-1,2,4-triazol-3-one

: 105-39-5
chloroacetic acid ethyl ester

: 1245623-60-2
ethyl [3-(5-chloro-2-thienyl)-4-(2-methoxyethyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]acetate

Conditions

Conditions	Yield
With potassium carbonate In acetonitrile at 80℃; for 6.5h;	100%
With potassium carbonate In acetonitrile at 80℃; for 6.5h;	100%
With potassium carbonate In acetonitrile at 80℃; for 6.5h;	100%

: 7480-35-5, 13286-59-4, 74165-73-4, 126456-43-7, 136030-00-7, 140632-19-5, 140632-20-8
(1S,2R)-1-amino-2-indanol

: 105-39-5
chloroacetic acid ethyl ester

: 862095-79-2
indeno[2,1-b]-1,4-oxazin-3(2H)-one,4,4a,9,9a-tetrahydro-,(4aR,9aS)-

Conditions

Conditions	Yield
Stage #1: (1S,2R)-1-amino-2-indanol With sodium hydride In tetrahydrofuran at 0 - 70℃; for 0.666667h; Stage #2: chloroacetic acid ethyl ester In tetrahydrofuran for 2.5h; Heating / reflux;	100%
With sodium hydride In tetrahydrofuran	85%

: 1539-42-0
bis[(2-pyridyl)methyl]amine

: 105-39-5
chloroacetic acid ethyl ester

: ethyl 2-(bis(pyridin-2-ylmethyl)amino)acetate

Conditions

Conditions	Yield
With sodium carbonate In acetonitrile for 18h; Reflux;	100%
Stage #1: bis[(2-pyridyl)methyl]amine With sodium hydrogencarbonate In acetonitrile for 0.166667h; Stage #2: chloroacetic acid ethyl ester In acetonitrile for 5h; Reflux; Inert atmosphere;
With triethylamine In ethanol for 12h; Reflux;

: 105-39-5
chloroacetic acid ethyl ester

: 38663-85-3
2-methoxyethyl isothiocyanate

: 589-16-2
4-aminoethylbenzene

: (Z)-2-((4-ethylphenyl)imino)-3-(2-methoxyethyl)thiazolidin-4-one

Conditions

Conditions	Yield
Stage #1: 2-methoxyethyl isothiocyanate; 4-aminoethylbenzene In ethanol at 78℃; for 12h; Knoevenagel Condensation; Stage #2: chloroacetic acid ethyl ester With sodium acetate In ethanol at 78℃; for 5h; regioselective reaction;	100%

...Expand

: 621-36-3
m-methylphenylacetic acid

: 105-39-5
chloroacetic acid ethyl ester

: C13H16O4

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran for 16h; Reflux; Inert atmosphere;	100%

: 28668-95-3
3-mercapto-5H-1,2,4-triazino[5,6-b]indole

: 105-39-5
chloroacetic acid ethyl ester

: 189325-51-7
ethyl ester of (1,2,4-triazino[5,6-b]indolyl-3-thio)acetic acid

Conditions

Conditions	Yield
With sodium In methanol; N,N-dimethyl-formamide at 60 - 100℃; for 15h; Alkylation;	99.5%
Stage #1: 3-mercapto-5H-1,2,4-triazino[5,6-b]indole With potassium carbonate microwave irradiation; Stage #2: chloroacetic acid ethyl ester for 0.0416667h; microwave irradiation;	89%

: 106-41-2
4-bromo-phenol

: 105-39-5
chloroacetic acid ethyl ester

: 6964-29-0
ethyl 2-(4-bromophenoxy)acetate

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 80℃;	99.3%
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 4h;	99%
With potassium carbonate In acetone Reflux;	87%

: 75-21-8
oxirane

: [4-(diethylamino)phenyl]dichlorophosphine

: 105-39-5
chloroacetic acid ethyl ester

: ethyl [4-(diethylamino)phenyl](2-chloroethoxy)phosphoryl acetate

Conditions

Conditions	Yield
at -5 - 20℃; for 2h; Inert atmosphere;	99.3%

...Expand

: 540-38-5
4-Iodophenol

: 105-39-5
chloroacetic acid ethyl ester

: 90794-33-5
4-iodophenoxyacetic acid ethyl ester

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 20℃; Inert atmosphere; Schlenk technique;	99%
With potassium carbonate In N,N-dimethyl-formamide for 16h;	98%
With potassium carbonate In N,N-dimethyl-formamide at 20℃;	96%
With potassium carbonate In N,N-dimethyl-formamide at 20℃;
With potassium carbonate In N,N-dimethyl-formamide at 20℃;

: 52542-59-3, 192520-17-5
bis(triphenylphosphineiminium) pentacarbonylmanganate(1-)

: 105-39-5
chloroacetic acid ethyl ester

A: 10170-69-1
dimanganese decacarbonyl

B: 14100-30-2
pentacarbonylchloromanganese(I)

C: η1-(CH2COOEt) manganese pentacarbonyl

Conditions

Conditions	Yield
In tetrahydrofuran (N2 or Ar); 25°C, rapid mixing; determination by NMR;	A 1% B 0% C 99%
In chloroform-d1 (N2 or Ar); 25°C, rapid mixing; determination by NMR;	A 1% B 0% C 99%

...Expand

: 66129-30-4
6-phenyl-[1,2,4]triazolo[4,3-b]pyridazine-3(2H)-thione

: 105-39-5
chloroacetic acid ethyl ester

: 1033038-23-1
ethyl-2-(6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylsulfanyl)acetate

Conditions

Conditions	Yield
With sodium hydroxide In ethanol at 20℃; for 3h;	99%

: 946415-03-8
C19H20N2

: 105-39-5
chloroacetic acid ethyl ester

: 1255528-61-0
C23H27N2O2(1+)*I(1-)

Conditions

Conditions	Yield
With sodium iodide In acetone at 20℃; for 18h;	99%

: 16714-25-3
2-azidobenzaldehyde

: 105-39-5
chloroacetic acid ethyl ester

: C11H11N3O3

Conditions

Conditions	Yield
With sodium In ethanol at 20℃; for 4h;	99%

: 40064-34-4
piperidine-4,4-diol hydrochloride

: 105-39-5
chloroacetic acid ethyl ester

: ethyl 2-(4-oxopiperidin-1-yl)acetate

Conditions

Conditions	Yield
With potassium carbonate In acetonitrile at 75℃;	99%

: 103027-41-4
1-(tert-butyldimethylsilyl)-4-(4',4',5',5'-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indol-5-ol

: 105-39-5
chloroacetic acid ethyl ester

: C14H13IO3

Conditions

Conditions	Yield
With potassium carbonate In acetone at 115℃; for 2h;	99%

: 5150-42-5
2,3-dimethoxyphenol

: 105-39-5
chloroacetic acid ethyl ester

: 861085-96-3
ethyl (2,3-dimethoxyphenoxy)acetate

Conditions

Conditions	Yield
Stage #1: 2,3-dimethoxyphenol With sodium hydride In tetrahydrofuran; dimethyl sulfoxide at 0℃; for 0.5h; Inert atmosphere; Stage #2: chloroacetic acid ethyl ester In tetrahydrofuran; dimethyl sulfoxide at 20℃; for 15h; Inert atmosphere;	98.8%