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Dayang Chem (Hangzhou) Co.,Ltd.

Dayangchem's 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. DayangChem can provide different quantities

2-(1-Methyl-2-oxopropyl)-1H-isoindole-1,3-(2H)-dione Manufacturer/High quality/Best price/In stock

Cas:2028-33-3

Min.Order:1 Kilogram

FOB Price: $3.0

Type:Lab/Research institutions

inquiry

Hangzhou J&H Chemical Co., Ltd.

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

1H-Isoindole-1,3(2H)-dione,2-(1-methyl-2-oxopropyl)-

Cas:2028-33-3

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Zibo Hangyu Biotechnology Development Co., Ltd

Zibo 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

1H-Isoindole-1,3(2H)-dione,2-(1-methyl-2-oxopropyl)-

Cas:2028-33-3

Min.Order:10 Gram

Negotiable

Type:Lab/Research institutions

inquiry

Henan Tianfu Chemical Co., Ltd.

Product Name: 2-(1-Methyl-2-oxopropyl)-1H-isoindole-1,3-(2H)-dione Synonyms: N-[3-BUTANONE(2)]-PHTHALIMIDE;2-(1-Methyl-2-Oxopropyl)-1h-Isoindole-1,3(2h)-Dione;N-(1-Methyl-2-oxopropyl)phthalimide CAS: 2028-33-3 MF: C12H11NO3 MW: 217.22 EINECS:

2028-33-3

Cas:2028-33-3

Min.Order:1 Gram

Negotiable

Type:Lab/Research institutions

inquiry

GIHI CHEMICALS CO.,LIMITED

high purity,in stock Package:25kg/drum,or as per customers'demand Application:API,or Intermediates,fine chemicals Transportation:air,sea,courier

N-(1-Methyl-2-oxo-propyl)phthalimide

Cas:2028-33-3

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Henan Allgreen Chemical Co.,Ltd

high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea

2-(1-Methyl-2-oxopropyl)-1H-isoindole-1,3-(2H)-dione

Cas:2028-33-3

Min.Order:0

Negotiable

Type:Manufacturers

inquiry

Antimex Chemical Limied

factory?direct?sale Application:healing drugs

1H-Isoindole-1,3(2H)-dione,2-(1-methyl-2-oxopropyl)-

Cas:2028-33-3

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Hangzhou Fandachem Co.,Ltd

2-(1-Methyl-2-oxopropyl)-1H-isoindole-1,3-(2H)-dione cas 2028-33-3Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express

2-(1-Methyl-2-oxopropyl)-1H-isoindole-1,3-(2H)-dione cas 2028-33-3

Cas:2028-33-3

Min.Order:0

Negotiable

Type:Other

inquiry

Amadis Chemical Co., Ltd.

1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G

2-(3-oxobutan-2-yl)isoindole-1,3-dione

Cas:2028-33-3

Min.Order:10 Milligram

Negotiable

Type:Lab/Research institutions

inquiry

HENAN SUNLAKE ENTERPRISE CORPORATION

2-(1-Methyl-2-oxopropyl)-1H-isoindole-1,3-(2H)-dione Basic information Product Name: 2-(1-Methyl-2-oxopropyl)-1H-isoindole-1,3-(2H)-dione Synonyms: N-[3-BUTANONE(2)]-PHTHALIMIDE;2-(1-Methyl-2-Oxopropyl)-1

2-(1-Methyl-2-oxopropyl)-1H-isoindole-1,3-(2H)-dione

Cas:2028-33-3

Min.Order:1 Kilogram

Negotiable

Type:Trading Company

inquiry

NovaChemistry

high purity Application:Drug intermediates Materials intermediates and active molecules

2-(3-oxobutan-2-yl)isoindole-1,3-dione

Cas:2028-33-3

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Synthetic route

potassium phtalimide
1074-82-4

potassium phtalimide

3-bromo-butanone
814-75-5

3-bromo-butanone

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

Conditions
ConditionsYield
at 20℃; for 0.233333h; Ionic liquid;96%
In N,N-dimethyl-formamide at 20℃;
3-chloro-2-butanone
4091-39-8

3-chloro-2-butanone

potassium phtalimide
1074-82-4

potassium phtalimide

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20 - 25℃; for 8h; Temperature;95%
In N,N-dimethyl-formamide at 20℃;
In N,N-dimethyl-formamide at 20℃; for 3h;
In N,N-dimethyl-formamide at 20℃;
2-(2-hydroxy-1-methyl-propyl)-isoindole-1,3-dione

2-(2-hydroxy-1-methyl-propyl)-isoindole-1,3-dione

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

Conditions
ConditionsYield
With manganese(IV) oxide; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; 2,6-Di-tert-butyl-1,4-benzoquinone In acetone at 65℃; for 17h; Temperature; Inert atmosphere;80%
2-(1-methylallyl)isoindole-1,3-dione
7065-05-6

2-(1-methylallyl)isoindole-1,3-dione

A

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

B

2-(1,3-dioxoisoindolin-2-yl)butan-4-al
4667-80-5

2-(1,3-dioxoisoindolin-2-yl)butan-4-al

Conditions
ConditionsYield
With bis(benzonitrile)palladium(II) dichloride; silver(I) nitrite; copper(II) choride dihydrate; nitromethane; oxygen; tert-butyl alcohol at 20℃; under 760.051 Torr; for 6h; Wacker Oxidation;A n/a
B 79%
methyllithium
917-54-4

methyllithium

2-phthalimidopropionic acid
21860-84-4

2-phthalimidopropionic acid

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

Conditions
ConditionsYield
In tetrahydrofuran; diethyl ether at -70 - 20℃; for 1h; Temperature;62%
N-acetonylphthalimide
3416-57-7

N-acetonylphthalimide

methyl iodide
74-88-4

methyl iodide

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

Conditions
ConditionsYield
With N,N,N,N,N,N-hexamethylphosphoric triamide; lithium diisopropyl amide at 60℃; for 17h;
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

3-Amino-2-butanone hydrochloride
21419-24-9

3-Amino-2-butanone hydrochloride

Conditions
ConditionsYield
With hydrogenchloride In acetic acid Heating;
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

2-hydroxymethyl-N-(2-hydroxy-1-methylpropyl)-benzamide

2-hydroxymethyl-N-(2-hydroxy-1-methylpropyl)-benzamide

Conditions
ConditionsYield
With sodium borohydrid In aqueous propan-2-ol; water; acetic acid
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

D,L-1-bromo-3-phthalimido-2-butanone
70386-38-8

D,L-1-bromo-3-phthalimido-2-butanone

Conditions
ConditionsYield
With bromine In water; acetic acid at 20℃;
With bromine; acetic acid at 20℃;
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

C21H16N4O2S
1240790-62-8

C21H16N4O2S

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: bromine; acetic acid / 20 °C
2.1: ethanol / 20 °C
2.2: Reflux
3.1: sodium hydrogencarbonate / ethanol / Reflux
View Scheme
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

C21H20N4O6S
1240790-63-9

C21H20N4O6S

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: bromine; acetic acid / 20 °C
2.1: ethanol / 20 °C
2.2: Reflux
3.1: Reflux
View Scheme
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

C20H15N5O2S
1240790-64-0

C20H15N5O2S

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: bromine; acetic acid / 20 °C
2: sodium hydrogencarbonate / ethanol / Reflux
View Scheme
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

C13H11N3O2S
1240790-65-1

C13H11N3O2S

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: bromine; acetic acid / 20 °C
2: sodium hydrogencarbonate / ethanol / Reflux
View Scheme
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

C19H15N3O2S
1240790-66-2

C19H15N3O2S

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: bromine; acetic acid / 20 °C
2: sodium hydrogencarbonate / ethanol / Reflux
View Scheme
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

C15H13N3O3S

C15H13N3O3S

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: bromine; acetic acid / 20 °C
2: sodium hydrogencarbonate / ethanol / Reflux
View Scheme
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

C20H15N3O3S

C20H15N3O3S

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: bromine; acetic acid / 20 °C
2: sodium hydrogencarbonate / ethanol / Reflux
View Scheme
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

C20H17N3O2S
1240790-69-5

C20H17N3O2S

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: bromine; acetic acid / 20 °C
2: sodium hydrogencarbonate / ethanol / Reflux
View Scheme
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

C25H19N3O2S
1240790-70-8

C25H19N3O2S

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: bromine; acetic acid / 20 °C
2: sodium hydrogencarbonate / ethanol / Reflux
View Scheme
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

C20H16N4O2S
1240790-71-9

C20H16N4O2S

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: bromine; acetic acid / 20 °C
2: sodium hydrogencarbonate / ethanol / Reflux
View Scheme
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

C19H15N5O2S
1240790-72-0

C19H15N5O2S

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: bromine; acetic acid / 20 °C
2: sodium hydrogencarbonate / ethanol / Reflux
View Scheme
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

C22H15NO3
1240790-59-3

C22H15NO3

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: bromine; acetic acid / 20 °C
2.1: potassium carbonate / acetone / Reflux
2.2: Reflux
View Scheme
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

C23H21NO7
1240790-60-6

C23H21NO7

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: bromine; acetic acid / 20 °C
2: potassium carbonate / acetone / Reflux
View Scheme
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

C17H13N3O2
1240790-61-7

C17H13N3O2

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: bromine; acetic acid / 20 °C
2: sodium hydrogencarbonate / butan-1-ol / Reflux
View Scheme
2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione
2028-33-3

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

BrH*C13H12N4O2S

BrH*C13H12N4O2S

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: bromine; acetic acid / 20 °C
2.1: ethanol / 20 °C
2.2: Reflux
View Scheme

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