5-Bromo-2-[(4-bromobenzyl)oxy]benzaldehyde

Base Information

Chemical Name:5-Bromo-2-[(4-bromobenzyl)oxy]benzaldehyde
CAS No.:84102-43-2
Molecular Formula:C14H10Br2O2
Molecular Weight:370.04
Hs Code.:2913000090
DSSTox Substance ID:DTXSID50399916
Wikidata:Q82202693
Mol file:84102-43-2.mol

Synonyms:5-bromo-2-[(4-bromobenzyl)oxy]benzaldehyde;84102-43-2;5-bromo-2-[(4-bromophenyl)methoxy]benzaldehyde;5-Bromo-2-((4-bromobenzyl)oxy)benzaldehyde;DTXSID50399916;BBL014029;MFCD02629607;STK199053;AKOS000287391;VS-04126;CS-0319369

Suppliers and Price of 5-Bromo-2-[(4-bromobenzyl)oxy]benzaldehyde

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

Matrix Scientific
5-Bromo-2-[(4-bromobenzyl)oxy]benzaldehyde
500mg
$ 95.00

Crysdot
5-Bromo-2-((4-bromobenzyl)oxy)benzaldehyde 97%
5g
$ 455.00

Biosynth Carbosynth
5-Bromo-2-[(4-bromobenzyl)oxy]benzaldehyde
1 g
$ 170.00

Biosynth Carbosynth
5-Bromo-2-[(4-bromobenzyl)oxy]benzaldehyde
250 mg
$ 57.50

Biosynth Carbosynth
5-Bromo-2-[(4-bromobenzyl)oxy]benzaldehyde
2 g
$ 289.00

AK Scientific
5-Bromo-2-[(4-bromobenzyl)oxy]benzaldehyde
500mg
$ 178.00

Total 5 raw suppliers

Chemical Property of 5-Bromo-2-[(4-bromobenzyl)oxy]benzaldehyde

Chemical Property:

PSA：26.30000
LogP:4.60310
XLogP3:4.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:369.90271
Heavy Atom Count:18
Complexity:265

Purity/Quality:

98%min ^*data from raw suppliers

5-Bromo-2-[(4-bromobenzyl)oxy]benzaldehyde ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1COC2=C(C=C(C=C2)Br)C=O)Br

Technology Process of 5-Bromo-2-[(4-bromobenzyl)oxy]benzaldehyde

There total 2 articles about 5-Bromo-2-[(4-bromobenzyl)oxy]benzaldehyde 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:

: 589-17-3
p-bromobenzyl chloride

: 1761-61-1
5-bromosalicyclaldehyde

: 84102-43-2
5-Brom-2-(4-brombenzyloxy)benzaldehyd

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 60 ℃; for 2h;
DOI:10.1016/j.bmcl.2006.09.052

Reference yield:

: 589-15-1
1-bromomethyl-4-bromobenzene

: 1761-61-1
5-bromosalicyclaldehyde

: 84102-43-2
5-Brom-2-(4-brombenzyloxy)benzaldehyd

Guidance literature:: With sodium ethanolate; potassium iodide; Yield given. Multistep reaction; 1) ethanol, 30 min, 80 deg C, DMF; 2) DMF, 2 h, reflux;