1-Acetyl-6-aminoindoline

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Company Name: J & K SCIENTIFIC LTD.  
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Company Name: Wuhan Chemwish Technology Co., Ltd  
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Company Name: Shanghai Sinch Parmaceuticals Tech. Co. Ltd.  
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Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
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1-Acetyl-6-aminoindoline manufacturers
1-Acetyl-6-aminoindoline Basic information
Product Name:1-Acetyl-6-aminoindoline
Synonyms:1-(6-Aminoindolin-1-yl)ethanone;1-Acetyl-6-amino-2,3-dihydro-1H-indole, 1-Acetyl-2,3-dihydro-1H-indol-6-amine;Ethanone, 1-(6-aMino-2,3-dihydro-1H-indol-1-yl)-;1-(6-Amino-2,3-dihydro-indol-1-yl)ethanone;1-Acetyl-6-amino-2,3-dihydroindole;6-Amino-N-acetylindoline;NSC 87623;1-(6-amino-1-indolinyl)ethanone
CAS:62368-29-0
MF:C10H12N2O
MW:176.22
EINECS:
Product Categories:Building Blocks;Heterocyclic Building Blocks;Indoles;Heterocyclic Compounds;Building Blocks
Mol File:62368-29-0.mol
1-Acetyl-6-aminoindoline Structure
1-Acetyl-6-aminoindoline Chemical Properties
Melting point 182 °C
storage temp. 2-8°C
form powder
color yellow to tan
InChI1S/C10H12N2O/c1-7(13)12-5-4-8-2-3-9(11)6-10(8)12/h2-3,6H,4-5,11H2,1H3
InChIKeyLOZKZWIQDVEDCQ-UHFFFAOYSA-N
SMILESCC(=O)N1CCc2ccc(N)cc12
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22
WGK Germany 3
Hazard Note Irritant
HS Code 2933998090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
ProviderLanguage
SigmaAldrich English
1-Acetyl-6-aminoindoline Usage And Synthesis
UsesReactant for preparation of:
  • Transient receptor potential cation channel V1 (TRPV1) antagonists
  • Inhibitor of the human immunodeficiency virus (HIV) envelope glycoprotein gp120 binding to the cluster of differentiation 4 (CD4) receptor
  • Antiproliferative agents
  • Serotonin 5-HT2C/2B receptor antagonists
Uses1-Acetyl-6-aminoindoline is a reactant in the synthesis of anilines, phenols, and heterocycles with aryl iodides.
1-Acetyl-6-aminoindoline Preparation Products And Raw materials
Preparation Products6-iodo-1H-indole-3-carbaldehyde
Tag:1-Acetyl-6-aminoindoline(62368-29-0) Related Product Information
1-Acetyl-6-aminoindoline 6-Aminoindole 1-Acetyl-5-amino-2,3-dihydro-(1H)-indole 1-Acetyl-6-amino-3,3-dimethyl-2,3-dihydro-indole 1-(3,3-Dimethyl-6-nitroindolin-1-yl)ethanone 1-Acetyl-N-(1-benzylpiperidin-4-yl)-indolin-6-amine N-(1-Acetyl-2,3-dihydro-(1H)-indol-6-yl)-N-(1-benzylpiperidin-4-yl)thiophene-2-carboxamide N-(1-Acetyl-2,3-dihydro-(1H)-indol-6-yl)-N-(1-benzylpiperidin-4-yl)-2,2-dimethylpropanamide N-(1-Acetyl-2,3-dihydro-(1H)-indol-6-yl)-N-(1-benzylpiperidin-4-yl)-3-(trifluoromethyl)benzamide N-(1-Acetyl-2,3-dihydro-(1H)-indol-6-yl)-4-tert-butylbenzenesulphonamide N-(1-Acetyl-2,3-dihydro-(1H)-indol-6-yl)benzenesulphonamide 1-Acetyl-N-(1-methylpiperidin-4-yl)-2,3-dihydro-(1H)-indole-6-amine N-(1-Acetyl-2,3-dihydro-(1H)-indol-6-yl)-4-chlorobenzenesulphonamide N-(1-Acetyl-2,3-dihydro-(1H)-indol-6-yl)-N-(1-benzylpiperidin-4-yl)-4-tert-butylbenzenesulphonamide N-(1-Acetyl-2,3-dihydro-(1H)-indol-6-yl)-N-(1-methylpiperidin-4-yl)thiophene-2-carboxamide N-(1-Acetyl-2,3-dihydro-(1H)-indol-6-yl)-N-(1-benzylpiperidin-4-yl)-4-methoxybenzenesulphonamide N-(1-Acetyl-2,3-dihydro-(1H)-indol-6-yl)-N-(1-benzylpiperidin-4-yl)-N'-ethylurea N-(1-Acetyl-2,3-dihydro-(1H)-indol-6-yl)-2-oxo-1-benzopyran-6-sulphonamide