8-Bromonaphthalene-2-carbaldehyde

Base Information

Chemical Name:8-Bromonaphthalene-2-carbaldehyde
CAS No.:841259-41-4
Molecular Formula:C₁₁H₇BrO
Molecular Weight:235.08
Hs Code.:2913000090
DSSTox Substance ID:DTXSID20461290
Wikidata:Q82285566
Mol file:841259-41-4.mol

Synonyms:8-bromo-2-naphthaldehyde;841259-41-4;8-bromonaphthalene-2-carbaldehyde;8-bromo-naphthalene-2-carbaldehyde;8-Bromonaphthalene-2-carboxaldehyde;2-Naphthalenecarboxaldehyde, 8-bromo-;DTXSID20461290;MFCD09029700;AKOS015962701;FD10668;AS-48873;AM20041230

Suppliers and Price of 8-Bromonaphthalene-2-carbaldehyde

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

American Custom Chemicals Corporation
8-BROMONAPHTHALENE-2-CARBALDEHYDE 95.00%
5MG
$ 496.84

Alichem
8-Bromonaphthalene-2-carboxaldehyde
1g
$ 1853.50

Alichem
8-Bromonaphthalene-2-carboxaldehyde
500mg
$ 980.00

Total 2 raw suppliers

Chemical Property of 8-Bromonaphthalene-2-carbaldehyde

Chemical Property:

PSA：17.07000
LogP:3.41480
XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:233.96803
Heavy Atom Count:13
Complexity:193

Purity/Quality:

99% ^*data from raw suppliers

8-BROMONAPHTHALENE-2-CARBALDEHYDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C(C=C(C=C2)C=O)C(=C1)Br

Technology Process of 8-Bromonaphthalene-2-carbaldehyde

There total 2 articles about 8-Bromonaphthalene-2-carbaldehyde 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: 72.0%

: 98331-27-2
8-bromo-2-(bromomethyl)naphthalene

: 841259-41-4
8-bromonaphthalene-2-carbaldehyde

Guidance literature:: With 2-nitropropane; sodium ethanolate; In ethanol; at 20 ℃; for 65h;
DOI:10.1021/jm049256w

Reference yield:

: 7511-27-5
1-bromo-7-methylnaphthalene

: 841259-41-4
8-bromonaphthalene-2-carbaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / N-bromosuccinimide; benzoyl peroxide / CCl₄ / 40 h / 75 °C

2: 72 percent / 2-nitropropane; NaOEt / ethanol / 65 h / 20 °C

With N-Bromosuccinimide; 2-nitropropane; sodium ethanolate; dibenzoyl peroxide; In tetrachloromethane; ethanol;
DOI:10.1021/jm049256w