3-Bromopropanal

Base Information Edit

Chemical Name:3-Bromopropanal
CAS No.:65032-54-4
Molecular Formula:C3H5BrO
Molecular Weight:136.976
Hs Code.:
DSSTox Substance ID:DTXSID60499350
Nikkaji Number:J2.640.693E
Mol file:65032-54-4.mol

Synonyms:3-bromopropanal;Propanal, 3-bromo-;65032-54-4;3-bromopropionaldehyde;SCHEMBL79305;DTXSID60499350;WGKZCFPJVPNRAV-UHFFFAOYSA-N;EN300-1717252;A936823

Suppliers and Price of 3-Bromopropanal

Supply Marketing:Edit

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 9 raw suppliers

Chemical Property of 3-Bromopropanal Edit

Chemical Property:

XLogP3:0.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:135.95238
Heavy Atom Count:5
Complexity:28.1

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C(CBr)C=O

Technology Process of 3-Bromopropanal

There total 1 articles about 3-Bromopropanal 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:

: Oxo-phenyl-acetic acid 3-bromo-propyl ester

: 65032-54-4
3-bromopropanal

: 100-52-7
benzaldehyde

: Oxo-phenyl-acetic acid vinyl ester

Guidance literature:: In benzene; Product distribution; Mechanism; Irradiation;
DOI:10.1021/jo971201x

Reference yield: 92.0%

: 65032-54-4
3-bromopropanal

: C₁₈H₂₇BrO₃Si

: C₁₈H₂₂Br₂O₃

Guidance literature:: With trityl tetrakis(pentafluorophenyl)borate; In dichloromethane; at 20 ℃; for 20h; enantioselective reaction; Inert atmosphere;
DOI:10.1039/c7cc00632b