1-Bromo-4-cyclohexylbenzene

Base Information Edit

Chemical Name:1-Bromo-4-cyclohexylbenzene
CAS No.:25109-28-8
Molecular Formula:C12H15Br
Molecular Weight:239.155
Hs Code.:29039990
European Community (EC) Number:246-623-3
NSC Number:67355
DSSTox Substance ID:DTXSID90179794
Nikkaji Number:J236.054C
Wikidata:Q72453908
Mol file:25109-28-8.mol

Synonyms:1-Bromo-4-cyclohexylbenzene;25109-28-8;P-BROMOCYCLOHEXYLBENZENE;C12H15Br;Benzene, 1-bromo-4-cyclohexyl-;1-bromo-4-cyclohexyl-benzene;EINECS 246-623-3;MFCD00019339;AI3-11173;NSC67355;4-Bromophenylcyclohexane;NCIOpen2_003485;SCHEMBL126116;C12-H15-Br;LVIJLEREXMVRAN-UHFFFAOYSA-;DTXSID90179794;NSC 67355;NSC-67355;AKOS005207316;CS-W014661;AS-37149;SY050256;B2686;FT-0607500;J-504444

Suppliers and Price of 1-Bromo-4-cyclohexylbenzene

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

TRC
1-Bromo-4-cyclohexylbenzene
50mg
$ 60.00

TCI Chemical
1-Bromo-4-cyclohexylbenzene
25G
$ 261.00

TCI Chemical
1-Bromo-4-cyclohexylbenzene
5G
$ 87.00

Frontier Specialty Chemicals
1-Bromo-4-cyclohexylbenzene 98%
5g
$ 125.00

Crysdot
1-Bromo-4-cyclohexylbenzene 97%
100g
$ 549.00

Chemenu
1-Bromo-4-cyclohexylbenzene 95+%
100g
$ 524.00

Biosynth Carbosynth
1-Bromo-4-cyclohexylbenzene
50 g
$ 595.00

Biosynth Carbosynth
1-Bromo-4-cyclohexylbenzene
100 g
$ 1034.00

Biosynth Carbosynth
1-Bromo-4-cyclohexylbenzene
25 g
$ 342.00

Biosynth Carbosynth
1-Bromo-4-cyclohexylbenzene
10 g
$ 171.00

Total 77 raw suppliers

Chemical Property of 1-Bromo-4-cyclohexylbenzene Edit

Chemical Property:

Appearance/Colour:Colorless to light yellow liquid
Vapor Pressure:0.00366mmHg at 25°C
Refractive Index:1.5595
Boiling Point:290.172 °C at 760 mmHg
Flash Point:127.852 °C
PSA：0.00000
Density:1.28 g/cm³
LogP:4.49680
Storage Temp.:Sealed in dry,Room Temperature
Water Solubility.:Not miscible or difficult to mix with water.
XLogP3:5.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:238.03571
Heavy Atom Count:13
Complexity:141

Purity/Quality:

99% ^*data from raw suppliers

1-Bromo-4-cyclohexylbenzene ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 24/25

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(CC1)C2=CC=C(C=C2)Br
Uses 1-Bromo-4-cyclohexylbenzene is used as a organic light-emitting diode and as a pharmaceutical intermediate.

Technology Process of 1-Bromo-4-cyclohexylbenzene

There total 31 articles about 1-Bromo-4-cyclohexylbenzene 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: 89.0%

: 589-87-7
1,4-bromoiodobenzene

: 1-cyclohexyl-2,4,6-triphenylpyridin-1-ium tetrafluoroborate salt

: 25109-28-8
4-bromo(cyclohexyl)benzene

Guidance literature:: With nickel(II) bromide dimethoxyethane; manganese; 4,4'-Dimethoxy-2,2'-bipyridin; In 1-methyl-pyrrolidin-2-one; at 15 ℃; for 20h; chemoselective reaction; Inert atmosphere;
DOI:10.1021/acs.orglett.9b01016

Reference yield: 87.0%

: 108-85-0
1-bromocyclohexane

: 5467-74-3
4-Bromophenylboronic acid

: 25109-28-8
4-bromo(cyclohexyl)benzene

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; tetrabutylammomium bromide; potassium carbonate; In water; toluene; at 80 ℃; for 4h; Inert atmosphere;

Reference yield: 85.0%

: 589-87-7
1,4-bromoiodobenzene

: 931-51-1
cyclohexylmagnesiumchloride

: 25109-28-8
4-bromo(cyclohexyl)benzene

Guidance literature:: With C₇₂H₆₃P₆Pd₃⁽¹⁺⁾*I^(1-); In tetrahydrofuran; toluene; at 20 ℃; for 2h; chemoselective reaction; Inert atmosphere; Glovebox;
DOI:10.1002/anie.201811380