Methyl 5-bromo-2-(bromomethyl)furan-3-carboxylate

Base Information Edit

Chemical Name:Methyl 5-bromo-2-(bromomethyl)furan-3-carboxylate
CAS No.:345891-29-4
Molecular Formula:C₇H₆Br₂O₃
Molecular Weight:297.931
Hs Code.:
DSSTox Substance ID:DTXSID701232455
Nikkaji Number:J1.493.128G
Mol file:345891-29-4.mol

Synonyms:methyl 5-bromo-2-(bromomethyl)furan-3-carboxylate;345891-29-4;SCHEMBL1674226;UDRDKZCLXJYHPY-UHFFFAOYSA-N;DTXSID701232455;EN300-23316167;Methyl 5-bromo-2-(bromomethyl)-3-furancarboxylate;5-Bromo-2-bromomethyl-furan-3-carboxylic Acid Methyl Ester

Suppliers and Price of Methyl 5-bromo-2-(bromomethyl)furan-3-carboxylate

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

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Chemical Property of Methyl 5-bromo-2-(bromomethyl)furan-3-carboxylate Edit

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:297.86632
Heavy Atom Count:12
Complexity:174

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC(=O)C1=C(OC(=C1)Br)CBr

Technology Process of Methyl 5-bromo-2-(bromomethyl)furan-3-carboxylate

There total 1 articles about Methyl 5-bromo-2-(bromomethyl)furan-3-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: 46.0%

: 6141-58-8
methyl 2-methyl-3-furancarboxylate

: 345891-28-3
methyl 5‐bromo‐2‐methylfuran‐3‐carboxylate

: 345891-29-4
methyl 5-bromo-2-(bromomethyl)furan-3-carboxylate

: 345891-27-2
methyl 5-bromo-2-(dibromomethyl)furan-3-carboxylate

Guidance literature:: With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; for 20h; Further Variations:; Reaction partners; Reagents; Solvents; Temperatures; reaction times; Product distribution; Heating;
DOI:10.1016/S0040-4039(01)00275-1