2-Bromo-1,2,3,4-tetrahydronaphthalene

Base Information

Chemical Name:2-Bromo-1,2,3,4-tetrahydronaphthalene
CAS No.:54753-94-5
Molecular Formula:C10H11Br
Molecular Weight:211.101
Hs Code.:
European Community (EC) Number:827-687-7
DSSTox Substance ID:DTXSID50512360

Synonyms:2-bromo-1,2,3,4-tetrahydronaphthalene;54753-94-5;MFCD12152091;SCHEMBL1243147;DTXSID50512360;AKOS010012384;SY297477;EN300-65304;F13406

Suppliers and Price of 2-Bromo-1,2,3,4-tetrahydronaphthalene

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
2-BROMO-1,2,3,4-TETRAHYDRONAPHTHALENE 95.00%
5G
$ 1928.08

American Custom Chemicals Corporation
2-BROMO-1,2,3,4-TETRAHYDRONAPHTHALENE 95.00%
2.5G
$ 1473.14

American Custom Chemicals Corporation
2-BROMO-1,2,3,4-TETRAHYDRONAPHTHALENE 95.00%
1G
$ 983.52

AK Scientific
2-Bromo-1,2,3,4-tetrahydronaphthalene
1g
$ 905.00

AK Scientific
2-Bromo-1,2,3,4-tetrahydronaphthalene
500mg
$ 710.00

Total 3 raw suppliers

Chemical Property of 2-Bromo-1,2,3,4-tetrahydronaphthalene

Chemical Property:

PSA：0.00000
LogP:2.93880
XLogP3:3.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:0
Exact Mass:210.00441
Heavy Atom Count:11
Complexity:133

Purity/Quality:

99% ^*data from raw suppliers

2-BROMO-1,2,3,4-TETRAHYDRONAPHTHALENE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC2=CC=CC=C2CC1Br

Technology Process of 2-Bromo-1,2,3,4-tetrahydronaphthalene

There total 4 articles about 2-Bromo-1,2,3,4-tetrahydronaphthalene 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: 5.7%

: 119-64-2
tetralin

: 75238-77-6
1-Bromo-1,2,3,4-tetrahydronaphthalene

: 54753-94-5
2-bromo-1,2,3,4-tetrahydronaphthalene

Guidance literature:: With styrene-4-vinyl(N-alkylpyridinium bromide); In water; acetic acid; at 23 ℃; for 24h;
DOI:10.1016/S0040-4020(01)85800-2

Reference yield:

: potassium 1,2,3,4-tetrahydro-2-naphthylpentafuorosilicate

: 54753-94-5
2-bromo-1,2,3,4-tetrahydronaphthalene

Guidance literature:: With N-Bromosuccinimide; 2,4,6-tri-tert-butylphenoxol; In 1,4-dioxane; at 50 ℃; for 16h; Yield given;
DOI:10.1246/bcsj.55.255

Reference yield:

: 91-13-4
α,α'-dibromo-o-xylene

: 54753-94-5
2-bromo-1,2,3,4-tetrahydronaphthalene

Guidance literature:: Multi-step reaction with 3 steps

1: 54 percent / Zn / acetonitrile / 4 h / 50 °C

2: 97 percent / KF / ethanol / Ambient temperature

3: 2,4,6-tri-t-butylphenol, NBS / dioxane / 16 h / 50 °C

With potassium fluoride; N-Bromosuccinimide; 2,4,6-tri-tert-butylphenoxol; zinc; In 1,4-dioxane; ethanol; acetonitrile;
DOI:10.1246/bcsj.55.255