5-bromo-1-propyl-1H-indole-2,3-dione

Base Information

• Chemical Name: 5-bromo-1-propyl-1H-indole-2,3-dione
• CAS No.: 312636-28-5
• Molecular Formula: C11H10BrNO2
• Molecular Weight: 268.10700
• DSSTox Substance ID: DTXSID90364986
• Nikkaji Number: J2.110.954A
• Wikidata: Q82149278
• Mol file: 312636-28-5.mol

Synonyms:5-bromo-1-propyl-1H-indole-2,3-dione;312636-28-5;5-bromo-1-propylindole-2,3-dione;5-Bromo-1-propylindoline-2,3-dione;5-bromo-1-propyl-2,3-dihydro-1H-indole-2,3-dione;SCHEMBL21001752;DTXSID90364986;MFCD01117162;STK122760;1-Propyl-5-bromoindoline-2,3-dione;AKOS000245404;CCG-104908;SB64753;5-bromo-1-propylindole-2,3(1h)-dione;LS-05307;CS-0308350;EU-0002621;EN300-116713;SR-01000409492;SR-01000409492-1;Z57392488;F0349-2913

Chemical Property of 5-bromo-1-propyl-1H-indole-2,3-dione

Chemical Property:

• PSA: 37.38000
• LogP: 2.45340
• XLogP3: 2.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 266.98949
• Heavy Atom Count: 15
• Complexity: 292

Purity/Quality:

98%min ^*data from raw suppliers

5-Bromo-1-propyl-1H-indole-2,3-dione ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCN1C2=C(C=C(C=C2)Br)C(=O)C1=O

Technology Process of 5-bromo-1-propyl-1H-indole-2,3-dione

There total 11 articles about 5-bromo-1-propyl-1H-indole-2,3-dione which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

5-bromo-3-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecane-1-sulfonyl)-1-propyl-1,3-dihydroindole-2-one (847550-40-7) → 5-bromo-1-propylindole-2,3(1H)-dione (312636-28-5)

Guidance literature:

With ammonium cerium(IV) nitrate; In water; acetonitrile; at 20 ℃; for 15h;

DOI:10.1002/chem.200601429

Reference yield: 92.0%

5-Bromo-1H-indole-2,3-dione (87-48-9) → 5-bromo-1-propylindole-2,3(1H)-dione (312636-28-5)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 80 ℃;

DOI:10.1016/j.ejmech.2010.07.020

Reference yield: 82.0%

5-Bromo-1H-indole-2,3-dione (87-48-9) + propyl bromide (106-94-5) → 5-bromo-1-propylindole-2,3(1H)-dione (312636-28-5)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; for 4h; Reflux;

DOI:10.1016/j.bioorg.2021.104748

upstream raw materials:

5-bromo-3-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecane-1-sulfonyl)-1-propyl-1,3-dihydroindole-2-one

5-bromo-3-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecane-1-sulfinyl)-1-propyl-1,3-dihydroindol-2-one

N-(4-bromo-phenyl)-2-oxo-N-propyl-acetamide

5-Bromo-1H-indole-2,3-dione

Downstream raw materials:

9-bromo-6-propyl-6H-indolo-[2,3-b]quinoxaline

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