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539-74-2 Usage

Chemical Properties

clear colorless to pale yellow liquid

Uses

Ethyl 3-bromopropionate was used in the preparation of (3?,4?-dimethoxyphenyl)-5-oxopentanoic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 539-74-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 539-74:
(5*5)+(4*3)+(3*9)+(2*7)+(1*4)=82
82 % 10 = 2
So 539-74-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H9BrO2/c1-2-8-5(7)3-4-6/h2-4H2,1H3

539-74-2 Well-known Company Product Price

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  • Alfa Aesar

  • (A12402)  Ethyl 3-bromopropionate, 99%   

  • 539-74-2

  • 25g

  • 718.0CNY

  • Detail
  • Alfa Aesar

  • (A12402)  Ethyl 3-bromopropionate, 99%   

  • 539-74-2

  • 100g

  • 2369.0CNY

  • Detail
  • Alfa Aesar

  • (A12402)  Ethyl 3-bromopropionate, 99%   

  • 539-74-2

  • 500g

  • 10003.0CNY

  • Detail

539-74-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 3-Bromopropionate

1.2 Other means of identification

Product number -
Other names Propanoic acid, 3-bromo-, ethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:539-74-2 SDS

539-74-2Synthetic route

ethyl acrylate
140-88-5

ethyl acrylate

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

Conditions
ConditionsYield
With hydrogen bromide In diethyl ether at 0 - 5℃; for 12h;99%
With diethyl ether; hydrogen bromide erst unter Eiskuehlung, zuletzt bei Raumtemperatur;
With hydrogen bromide
With hydrogen bromide; dibenzoyl peroxide In diethyl ether
Acetyl bromide
506-96-7

Acetyl bromide

ethyl acrylate
140-88-5

ethyl acrylate

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

Conditions
ConditionsYield
With hydroquinone In ethanol at 20 - 55℃; for 2h;91%
ethyl 3-chloropropanoate
623-71-2

ethyl 3-chloropropanoate

A

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

B

2-bromo-2’-chlorodiethyl ether
51070-66-7

2-bromo-2’-chlorodiethyl ether

Conditions
ConditionsYield
With sodium bromide; 1,2-dibromomethane In N,N-dimethyl-formamide at 100℃; for 6h;A 85%
B n/a
ethanol
64-17-5

ethanol

propyl methacrylate
2210-28-8

propyl methacrylate

A

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

B

3-bromo-2-methyl propionic acid n-propyl ester

3-bromo-2-methyl propionic acid n-propyl ester

Conditions
ConditionsYield
With Acetyl bromide; 2,5-bis(1,1-dimethylethyl)-1,4-benzenediol at 20 - 50℃; for 2h; Overall yield = 11.6 g;A n/a
B 53.4%
ethanol
64-17-5

ethanol

A

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

B

Methyl 3-bromopropionate
3395-91-3

Methyl 3-bromopropionate

Conditions
ConditionsYield
With Acetyl bromide; hydroquinone; ethyl acrylate at 20 - 50℃; for 2h; Overall yield = 88.5 g;A n/a
B 53%
methanol
67-56-1

methanol

ethyl acrylate
140-88-5

ethyl acrylate

A

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

B

Methyl 3-bromopropionate
3395-91-3

Methyl 3-bromopropionate

Conditions
ConditionsYield
With Acetyl bromide; hydroquinone at 20 - 55℃; for 2h; Overall yield = 92.3 g;A 51%
B n/a
ethyl bromoacetate
105-36-2

ethyl bromoacetate

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

Conditions
ConditionsYield
Zeitlicher Verlauf unter Belichtung;
3-Bromopropionic acid
590-92-1

3-Bromopropionic acid

ethanol
64-17-5

ethanol

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

Conditions
ConditionsYield
With tetrachloromethane; phenol-2-sulfonic acid und entfernt das entstehende Wasser kontinuierlich mittels einer geeigneten Vorrichtung;
With tetrachloromethane; 5-sulfosalicylic Acid und entfernt das entstehende Wasser kontinuierlich mittels einer geeigneten Vorrichtung;
With sulfuric acid
3-Bromopropionic acid
590-92-1

3-Bromopropionic acid

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

Conditions
ConditionsYield
durch Veresterung;
β-Propiolactone
57-57-8

β-Propiolactone

ethanol
64-17-5

ethanol

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

Conditions
ConditionsYield
With hydrogen bromide at 2 - 5℃;
cyclopropanone diethyl acetal
41330-13-6

cyclopropanone diethyl acetal

A

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

B

2,3-dibromopropionic acid ethyl ester
3674-13-3

2,3-dibromopropionic acid ethyl ester

Conditions
ConditionsYield
With tetrachloromethane; bromine
3-bromo-propionimidic acid ethyl ester; hydrobromide
98071-69-3

3-bromo-propionimidic acid ethyl ester; hydrobromide

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

Conditions
ConditionsYield
With water
acrylonitrile
107-13-1

acrylonitrile

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

Conditions
ConditionsYield
With water; hydrogen bromide Erwaermen des Reaktionsprodukts mit Tetrachlormethan,Aethanol und kleinen Mengen wss.Bromwasserstoffsaeure;
[(1-Ethoxycyclopropyl)oxy]trimethylsilane
27374-25-0

[(1-Ethoxycyclopropyl)oxy]trimethylsilane

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

Conditions
ConditionsYield
With bromine; titanium tetrachloride 1.) CH2Cl2, 25 deg C, 2.) CH2Cl2; Multistep reaction;
ethyl 3-(trichlorotitanio)propionate

ethyl 3-(trichlorotitanio)propionate

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

Conditions
ConditionsYield
With bromine In tetrachloromethane at 0℃;
silver ethyl succinate

silver ethyl succinate

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

Conditions
ConditionsYield
With tetrachloromethane; bromine
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

Ethyl nipecotate
71962-74-8

Ethyl nipecotate

ethyl 1-[2-(ethoxycarbonyl)ethyl]-3-piperidinecarboxylate
128200-19-1

ethyl 1-[2-(ethoxycarbonyl)ethyl]-3-piperidinecarboxylate

Conditions
ConditionsYield
With triethylamine In toluene Ambient temperature;100%
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

di-(2-exo-hydroxy-10-bornyl) diselenide
177171-54-9

di-(2-exo-hydroxy-10-bornyl) diselenide

3-((1S,2R,4R)-2-Hydroxy-7,7-dimethyl-bicyclo[2.2.1]hept-1-ylmethylselanyl)-propionic acid ethyl ester
218623-59-7

3-((1S,2R,4R)-2-Hydroxy-7,7-dimethyl-bicyclo[2.2.1]hept-1-ylmethylselanyl)-propionic acid ethyl ester

Conditions
ConditionsYield
With sodium tetrahydroborate In ethanol for 4h; Ambient temperature;100%
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

1,1-dideuterio-3-bromopropanol
81344-31-2

1,1-dideuterio-3-bromopropanol

Conditions
ConditionsYield
With lithium aluminium deuteride In tetrahydrofuran at 20℃; for 3h; Reduction;100%
Indole-3-carboxaldehyde
487-89-8

Indole-3-carboxaldehyde

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

3-(3-formyl-indol-1-yl)-propionic acid ethyl ester
503829-88-7

3-(3-formyl-indol-1-yl)-propionic acid ethyl ester

Conditions
ConditionsYield
With potassium carbonate In acetonitrile for 48h; Heating / reflux;100%
With potassium carbonate In acetonitrile for 48h; Heating / reflux;100%
With potassium carbonate In acetonitrile for 48h; Heating / reflux;100%
With potassium carbonate In acetonitrile for 48h; Heating / reflux;100%
With potassium carbonate In acetonitrile for 48h;
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

4-bromo-5-[(1R,2R,3R,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-ylamino]pyridazin-3(2H)-one
1149587-11-0

4-bromo-5-[(1R,2R,3R,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-ylamino]pyridazin-3(2H)-one

ethyl 3-{5-bromo-6-oxo-4-[(1R,2R,3R,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-ylamino]pyridazin-1(6H)-yl}propanoate
1149587-17-6

ethyl 3-{5-bromo-6-oxo-4-[(1R,2R,3R,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-ylamino]pyridazin-1(6H)-yl}propanoate

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 20 - 80℃; for 4h;100%
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

2,4-dihydro-4-[4-[4-(4-methoxyphenyl)-1-piperazinyl ]-phenyl]-3H-1,2,4-triazol-3-one
74853-07-9

2,4-dihydro-4-[4-[4-(4-methoxyphenyl)-1-piperazinyl ]-phenyl]-3H-1,2,4-triazol-3-one

ethyl 3-(4-(4-(4-(4-methoxyphenyl)piperazin-1-yl)phenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl)propanoate

ethyl 3-(4-(4-(4-(4-methoxyphenyl)piperazin-1-yl)phenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl)propanoate

Conditions
ConditionsYield
Stage #1: Ethyl 3-bromopropionate With caesium carbonate In dimethyl sulfoxide at 20℃; for 0.5h; Inert atmosphere;
Stage #2: 2,4-dihydro-4-[4-[4-(4-methoxyphenyl)-1-piperazinyl ]-phenyl]-3H-1,2,4-triazol-3-one In dimethyl sulfoxide at 90℃; for 12h; Inert atmosphere;
100%
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

ethyl 3-nitrooxy propionate
100550-00-3

ethyl 3-nitrooxy propionate

Conditions
ConditionsYield
With silver nitrate In acetonitrile at 70℃; for 5h; Darkness;99.7%
With silver nitrate; acetonitrile
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

diphenyl diselenide
1666-13-3

diphenyl diselenide

Ethyl 3-(Phenylseleno)propionate
109179-39-7

Ethyl 3-(Phenylseleno)propionate

Conditions
ConditionsYield
With potassium dihydrogenphosphate; zinc In water; acetonitrile for 1h;98%
With indium In tetrahydrofuran; water at 25℃; for 5h;76%
With cerium; iodine 1a) THF, r.t., 30 min, 1b) 35 deg C, 30 min, 2) 25-35-deg C, 5h; Yield given. Multistep reaction;
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

saccharin
81-07-2

saccharin

2-(2'-Ethoxycarbonylethyl)-saccharin
83747-24-4

2-(2'-Ethoxycarbonylethyl)-saccharin

Conditions
ConditionsYield
With water; potassium carbonate In N,N-dimethyl-formamide for 6h; Heating;98%
With sodium hydrogencarbonate In N,N-dimethyl-formamide at 60 - 80℃; for 4h;
allyl 2-oxo-4-(phenylthio)cyclohex-3-enecarboxylate
900493-69-8

allyl 2-oxo-4-(phenylthio)cyclohex-3-enecarboxylate

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

allyl 1-(3-ethoxy-3-oxopropyl)-2-oxo-4-(phenylthio)cyclohex-3-enecarboxylate
900493-82-5

allyl 1-(3-ethoxy-3-oxopropyl)-2-oxo-4-(phenylthio)cyclohex-3-enecarboxylate

Conditions
ConditionsYield
Stage #1: allyl 2-oxo-4-(phenylthio)cyclohex-3-enecarboxylate With sodium hydride In tetrahydrofuran for 0.166667h; cooling;
Stage #2: Ethyl 3-bromopropionate In tetrahydrofuran at 20℃;
98%
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

4-iodobenzenesulfonyl chloride
98-61-3

4-iodobenzenesulfonyl chloride

ethyl 3-([4-iodophenyl]thio)propanoate

ethyl 3-([4-iodophenyl]thio)propanoate

Conditions
ConditionsYield
Stage #1: p-Iodobenzenesulfonyl chloride With triphenylphosphine In acetonitrile at 60℃; for 0.333333h; Inert atmosphere;
Stage #2: Ethyl 3-bromopropionate With potassium carbonate In water; acetonitrile for 20h; Inert atmosphere; Reflux;
98%
2-carbethoxyindole
3770-50-1

2-carbethoxyindole

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

ethyl 1-(3-ethoxy-3-oxopropyl)-1H-indole-2-carboxylate
256664-26-3

ethyl 1-(3-ethoxy-3-oxopropyl)-1H-indole-2-carboxylate

Conditions
ConditionsYield
With potassium carbonate In acetonitrile for 72h; Reflux;97%
With potassium carbonate In acetonitrile for 144h; Reflux;1.46 g
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochloride
1167415-79-3

7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochloride

ethyl 3-[7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1,4-benzoxazepin-4(5H)-yl]propanoate
1167416-62-7

ethyl 3-[7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1,4-benzoxazepin-4(5H)-yl]propanoate

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In acetonitrile at 80℃; Inert atmosphere;97%
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

N-<2-(3,5-difluoro-4-hydroxyphenylthio)ethyl>phthalimide
169298-43-5

N-<2-(3,5-difluoro-4-hydroxyphenylthio)ethyl>phthalimide

{4-[2-(1,3-dioxo-1,3-dihydroisoindol-2-yl)ethylsulfanyl]-2,6-difluorophenoxy}acetic acid ethyl ester
141286-84-2

{4-[2-(1,3-dioxo-1,3-dihydroisoindol-2-yl)ethylsulfanyl]-2,6-difluorophenoxy}acetic acid ethyl ester

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 25℃;97%
2-chlorothiphenol
6320-03-2

2-chlorothiphenol

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

ethyl 3-(2-chlorophenylthio)propionate

ethyl 3-(2-chlorophenylthio)propionate

Conditions
ConditionsYield
With potassium carbonate In ethanol at 80℃; for 1h; Temperature;97%
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

2-(piperidine-4-yl-2H-benzo[d][1,2,3]triazole)

2-(piperidine-4-yl-2H-benzo[d][1,2,3]triazole)

3-(4-benzotriazol-2-yl-piperidin-1-yl)-propionic acid ethyl ester
1384436-37-6

3-(4-benzotriazol-2-yl-piperidin-1-yl)-propionic acid ethyl ester

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃; for 4h;96%
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

ethyl 3-iodopropanoate
6414-69-3

ethyl 3-iodopropanoate

Conditions
ConditionsYield
With sodium iodide In butanone at 90℃; for 16h;95%
With sodium iodide In acetone for 14h; Reflux; Inert atmosphere;95%
With sodium iodide In acetone 1.) room temperature, 30 min, 2.) reflux, 30 min;94%
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
5466-88-6

3,4-dihydro-3-oxo-2H-1,4-benzoxazine

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

ethyl 3-(3-oxo-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)propanoate
23866-14-0

ethyl 3-(3-oxo-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)propanoate

Conditions
ConditionsYield
Stage #1: 3,4-dihydro-3-oxo-2H-1,4-benzoxazine With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 0.25h;
Stage #2: Ethyl 3-bromopropionate In N,N-dimethyl-formamide at 90℃;
95%
With potassium carbonate In N,N-dimethyl-formamide for 18h; Heating;91%
With sodium hydride In N,N-dimethyl-formamide at 20℃; for 3h;45%
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

1-(2-methoxyphenyl)piperazine hydrochloride
5464-78-8

1-(2-methoxyphenyl)piperazine hydrochloride

ethyl 3-(4-(2-methoxyphenyl)piperazin-1-yl)propanoate
56968-31-1

ethyl 3-(4-(2-methoxyphenyl)piperazin-1-yl)propanoate

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In acetonitrile at 60℃;95%
With potassium carbonate; potassium iodide In acetonitrile for 18h; Heating / reflux;71%
2-(3,4-Dichloro-phenyl)-5-(tetrahydro-pyran-4-yloxy)-pentanenitrile

2-(3,4-Dichloro-phenyl)-5-(tetrahydro-pyran-4-yloxy)-pentanenitrile

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

ammonium chloride

ammonium chloride

4-Cyano-4-(3,4-dichlorophenyl)-7-(tetrahydropyran-4-yloxy)-heptanoic acid ethyl ester

4-Cyano-4-(3,4-dichlorophenyl)-7-(tetrahydropyran-4-yloxy)-heptanoic acid ethyl ester

Conditions
ConditionsYield
With potassium hexamethylsilazane In tetrahydrofuran; toluene94.4%
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

6-(4-Fluoro-phenyl)-4-phenyl-2H-pyridazin-3-one
116776-59-1

6-(4-Fluoro-phenyl)-4-phenyl-2H-pyridazin-3-one

3-[3-(4-Fluoro-phenyl)-6-oxo-5-phenyl-6H-pyridazin-1-yl]-propionic acid ethyl ester
127661-94-3

3-[3-(4-Fluoro-phenyl)-6-oxo-5-phenyl-6H-pyridazin-1-yl]-propionic acid ethyl ester

Conditions
ConditionsYield
With sodium ethanolate In ethanol for 24h; Heating;94%
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

bis(2-carboxyethylethyl) diselenide
86247-54-3

bis(2-carboxyethylethyl) diselenide

Conditions
ConditionsYield
With dilithium diselenide In tetrahydrofuran at 5℃; for 0.333333h;94%
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

2-(3,4-dichloro-phenyl)-5-(tetrahydro-pyran-2-yl-oxy)-pentanenitrile
146395-96-2

2-(3,4-dichloro-phenyl)-5-(tetrahydro-pyran-2-yl-oxy)-pentanenitrile

4-Cyano-4-(3,4-dichloro-phenyl)-7-(tetrahydro-pyran-2-yloxy)-heptanoic acid ethyl ester
146395-97-3

4-Cyano-4-(3,4-dichloro-phenyl)-7-(tetrahydro-pyran-2-yloxy)-heptanoic acid ethyl ester

Conditions
ConditionsYield
With potassium hexamethylsilazane In tetrahydrofuran at -78℃;94%
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

6-nitro-4H-benzo[1,4]oxazin-3-one
81721-87-1

6-nitro-4H-benzo[1,4]oxazin-3-one

3-(6-nitro-3-oxo-2,3-dihydro-benzo[1,4]oxazin-4-yl)-propionic acid ethyl ester
475469-73-9

3-(6-nitro-3-oxo-2,3-dihydro-benzo[1,4]oxazin-4-yl)-propionic acid ethyl ester

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide at 40℃; for 0.3h; microwave irradiation;94%
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 10h;77%
With sodium hydride In N,N-dimethyl-formamide at 20℃; for 3h;65%
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 8h;
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

6,6'-disulfanediylbis[4-(3,5-dimethylphenoxy)benzene-1,3-diamine]
1232540-96-3

6,6'-disulfanediylbis[4-(3,5-dimethylphenoxy)benzene-1,3-diamine]

C19H24N2O3S
1232541-11-5

C19H24N2O3S

Conditions
ConditionsYield
With 1,8-diazabicyclo[5.4.0]undec-7-ene; ethanethiol In tetrahydrofuran at 20℃; for 0.0166667h;94%
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

phenylacetylene
536-74-3

phenylacetylene

(4-phenyl-1,2,3-triazole-1-yl)acetic acid ethyl ester
51720-17-3

(4-phenyl-1,2,3-triazole-1-yl)acetic acid ethyl ester

Conditions
ConditionsYield
With sodium azide; sodium 2-(1,2-dihydroxyethyl)-4-hydroxy-5-oxo-2,5-dihydro-furan-3-olate In water at 20℃; for 2h; Huisgen Cycloaddition; regiospecific reaction;94%
With sodium azide; sodium L-ascorbate In water; tert-butyl alcohol for 3h; Heating; Green chemistry;93%
With sodium azide; sodium L-ascorbate In water at 50℃; for 3.5h; Green chemistry;91%
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

N’-(pyridin-3-ylmethylene)isonicotinohydrazide
15017-31-9

N’-(pyridin-3-ylmethylene)isonicotinohydrazide

C22H28N4O5(2+)*2I(1-)

C22H28N4O5(2+)*2I(1-)

Conditions
ConditionsYield
With sodium iodide In acetonitrile for 0.0666667h; Microwave irradiation;94%
1-Methylpyrrolidine
120-94-5

1-Methylpyrrolidine

Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

1-(2-Ethoxycarbonyl-ethyl)-1-methyl-pyrrolidinium; bromide

1-(2-Ethoxycarbonyl-ethyl)-1-methyl-pyrrolidinium; bromide

Conditions
ConditionsYield
In neat (no solvent)93%
Ethyl 3-bromopropionate
539-74-2

Ethyl 3-bromopropionate

decylthiol
143-10-2

decylthiol

3-decylsulfanylpropionic acid ethyl ester
68749-04-2

3-decylsulfanylpropionic acid ethyl ester

Conditions
ConditionsYield
With potassium carbonate In dimethyl sulfoxide; acetone at 20℃; for 24h; Alkylation;93%

539-74-2Relevant articles and documents

Iron(II) and Copper(I) Control the Total Regioselectivity in the Hydrobromination of Alkenes

Cruz, Daniel A.,Sinka, Victoria,De Armas, Pedro,Steingruber, Hugo Sebastian,Fernández, Israel,Martín, Víctor S.,Miranda, Pedro O.,Padrón, Juan I.

supporting information, p. 6105 - 6109 (2021/08/18)

A new method that allows the complete control of the regioselectivity of the hydrobromination reaction of alkenes is described. Herein, we report a radical procedure with TMSBr and oxygen as common reagents, where the formation of the anti-Markovnikov product occurs in the presence of parts per million amounts of the Cu(I) species and the formation of the Markovnikov product occurs in the presence of 30 mol % iron(II) bromide. Density functional theory calculations combined with Fukui's radical susceptibilities support the obtained results.

Synthesis of N-Substituted phosphoramidic acid esters as “reverse” fosmidomycin analogues

Adeyemi, Christiana M.,Hoppe, Heinrich C.,Isaacs, Michelle,Klein, Rosalyn,Lobb, Kevin A.,Kaye, Perry T.

, p. 2371 - 2378 (2019/03/23)

An efficient synthetic pathway to a series of novel “reverse” fosmidomycin analogues has been developed, commencing from substituted benzylamines. In these analogues, the fosmidomycin hydroxamate moiety is reversed and the tetrahedral methylene carbon adjacent to the phosphonate moiety is replaced by a nitrogen atom bearing different benzyl groups. The resulting phosphonate esters were designed as potential antimalarial “pro-drugs”.

Antimicrobial poly(2-methyloxazoline)s with bioswitchable activity through satellite group modification

Krumm, Christian,Harmuth, Simon,Hijazi, Montasser,Neugebauer, Britta,Kampmann, Anne-Larissa,Geltenpoth, Helma,Sickmann, Albert,Tiller, Joerg C.

supporting information, p. 3830 - 3834 (2014/05/06)

Biocides are widely used for preventing the spread of microbial infections and fouling of materials. Since their use can build up microbial resistance and cause unpredictable long-term environmental problems, new biocidal agents are required. In this study, we demonstrate a concept in which an antimicrobial polymer is deactivated by the cleavage of a single group. Following the satellite group approach, a biocidal quaternary ammonium group was linked through a poly(2-methyloxazoline) to an ester satellite group. The polymer with an octyl-3-propionoate satellite group shows very good antimicrobial activity against Gram-positive bacterial strains. The biocidal polymer was also found to have low hemotoxicity, resulting in a high HC50/MIC value of 120 for S. aureus. Cleaving the ester satellite group resulted in a 30-fold decrease in antimicrobial activity, proving the concept valid. The satellite group could also be cleaved by lipase showing that the antimicrobial activity of the new biocidal polymers is indeed bioswitchable. Biocides are widely used for preventing the spread of microbial infections and the fouling of materials. Since their application can build up microbial resistance and cause unpredictable long-term environmental problems, new biocidal agents are required. In a novel approach an antimicrobial polymer is deactivated by hydrolysis of an ester group through the action of a lipase. The crucial feature is the mutual interaction of the two endgroups of the polymer.

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