1-Bromo-2-chloronaphthalene

Base Information

Chemical Name:1-Bromo-2-chloronaphthalene
CAS No.:71436-66-3
Molecular Formula:C10H6BrCl
Molecular Weight:241.515
Hs Code.:
European Community (EC) Number:849-426-6
DSSTox Substance ID:DTXSID70504323
Mol file:71436-66-3.mol

Synonyms:1-Bromo-2-chloronaphthalene;71436-66-3;chlorobromonaphthalene;SCHEMBL9720422;DTXSID70504323;MFCD17012389;BS-51139;CS-0141436;FT-0767873;E76484;EN300-3525636;Z1269176087

Suppliers and Price of 1-Bromo-2-chloronaphthalene

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

Alichem
1-Bromo-2-chloronaphthalene
1g
$ 1786.10

Alichem
1-Bromo-2-chloronaphthalene
500mg
$ 999.60

Alichem
1-Bromo-2-chloronaphthalene
250mg
$ 659.60

AK Scientific
1-Bromo-2-chloronaphthalene
100mg
$ 658.00

Total 13 raw suppliers

Chemical Property of 1-Bromo-2-chloronaphthalene

Chemical Property:

Melting Point:46 °C
Boiling Point:110 °C(Press: 21 Torr)
PSA：0.00000
Density:1.592±0.06 g/cm3(Predicted)
LogP:4.25570
XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:0
Exact Mass:239.93414
Heavy Atom Count:12
Complexity:160

Purity/Quality:

98% ^*data from raw suppliers

1-Bromo-2-chloronaphthalene ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=CC(=C2Br)Cl

Technology Process of 1-Bromo-2-chloronaphthalene

There total 1 articles about 1-Bromo-2-chloronaphthalene 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:

: 71436-63-0
1-bromo-3,4-benzo-6,6-dichlorobicyclo<3.1.0>hexane

: 865-47-4
potassium tert-butylate

: 91-58-7
2-chloronaphthalene

: 71436-67-4
2-bromo-3-chloronaphthalene

: 71436-68-5
1-tert-butoxy-2-chloronaphthalene

: 71436-69-6
2-tert-Butoxy-3-chloro-naphthalene

: 71436-70-9
1,3-Di-tert-butoxynaphthalin

: 71436-66-3
1-bromo-2-chloronaphthalene

Guidance literature:: In tetrahydrofuran; at 0 ℃; for 0.5h; Mechanism; Product distribution;
DOI:10.1021/jo01311a017

Reference yield:

: 71436-66-3
1-bromo-2-chloronaphthalene

: 109297-21-4
2--1-tolylsulphonyl-1a,7b-dihydro-1H-cyclopropa naphthalene-3-carbonitrile

Guidance literature:: Multi-step reaction with 2 steps

2: 62 percent / t-BuOK / dimethylformamide / 0.33 h / -40 °C

With potassium tert-butylate; In N,N-dimethyl-formamide;