ethyl 3,4-dibromo-5-methoxy-1H-indole-2-carboxylate

Base Information

Chemical Name:ethyl 3,4-dibromo-5-methoxy-1H-indole-2-carboxylate
CAS No.:30933-70-1
Molecular Formula:C12H11Br2NO3
Molecular Weight:
Hs Code.:
DSSTox Substance ID:DTXSID101223159

Synonyms:ethyl 3,4-dibromo-5-methoxy-1H-indole-2-carboxylate;30933-70-1;DTXSID101223159

Suppliers and Price of ethyl 3,4-dibromo-5-methoxy-1H-indole-2-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of ethyl 3,4-dibromo-5-methoxy-1H-indole-2-carboxylate

Chemical Property:

XLogP3:4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:376.90852
Heavy Atom Count:18
Complexity:316

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=O)C1=C(C2=C(N1)C=CC(=C2Br)OC)Br

Technology Process of ethyl 3,4-dibromo-5-methoxy-1H-indole-2-carboxylate

There total 2 articles about ethyl 3,4-dibromo-5-methoxy-1H-indole-2-carboxylate 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: 78.0%

: 4792-58-9
ethyl 5-methoxy-1H-indole-2-carboxylate

: 30933-70-1
ethyl 3,4-dibromo-5-methoxy-1H-indole-2-carboxylate

: 92622-96-3
ethyl 3-bromo-5-methoxy-1H-indole-2-carboxylate

: 30933-69-8
ethyl 4-bromo-5-methoxy-1H-indole-2-carboxylate

: ethyl 3,6-dibromo-5-methoxyindole-2-carboxylate

Guidance literature:: With bromine; In acetic acid; for 1h; Product distribution; Mechanism; Ambient temperature; other methoxy derivatives of ethyl indole-2-acrboxylate; pyridinium bromide perbromide or N-bromosuccinimide (NBS) as bromination agent; var. solvents, temperatures and reaction times;

Reference yield:

: 4792-58-9
ethyl 5-methoxy-1H-indole-2-carboxylate

: 30933-70-1
ethyl 3,4-dibromo-5-methoxy-1H-indole-2-carboxylate

: 92622-96-3
ethyl 3-bromo-5-methoxy-1H-indole-2-carboxylate

: 30933-69-8
ethyl 4-bromo-5-methoxy-1H-indole-2-carboxylate

Guidance literature:: With bromine; In acetic acid; for 0.00277778h; Product distribution; 30 s, 24 h or 24 h with sodium acetate buffer;
DOI:10.1021/jo00199a004