1-Bromobicyclo[1.1.1]pentane

Base Information

Chemical Name:1-Bromobicyclo[1.1.1]pentane
CAS No.:128884-80-0
Molecular Formula:C5H7Br
Molecular Weight:147.01300
Hs Code.:
DSSTox Substance ID:DTXSID60562750
Nikkaji Number:J595.540H
Wikidata:Q82447017
Mol file:128884-80-0.mol

Synonyms:1-Bromobicyclo[1.1.1]pentane;128884-80-0;Bicyclo[1.1.1]pentane, 1-bromo- (9CI);Bicyclo[1.1.1]pentane, 1-bromo-;DTXSID60562750;AKOS027470085;AB92159;CS-0067813;H11101;EN300-39924099

Suppliers and Price of 1-Bromobicyclo[1.1.1]pentane

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

Crysdot
1-bromobicyclo[1.1.1]pentane 95%
250mg
$ 2550.00

Crysdot
1-bromobicyclo[1.1.1]pentane 95%
100mg
$ 1336.00

ACHEMBLOCK
1-bromobicyclo[1.1.1]pentane 97%
1G
$ 3465.00

ACHEMBLOCK
1-bromobicyclo[1.1.1]pentane 97%
100MG
$ 1385.00

Total 11 raw suppliers

Chemical Property of 1-Bromobicyclo[1.1.1]pentane

Chemical Property:

Boiling Point:96 °C
PSA：0.00000
Density:1.864±0.06 g/cm3(Predicted)
LogP:1.93380
XLogP3:1.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:0
Exact Mass:145.97311
Heavy Atom Count:6
Complexity:70.9

Purity/Quality:

97% ^*data from raw suppliers

1-bromobicyclo[1.1.1]pentane 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C2CC1(C2)Br

Technology Process of 1-Bromobicyclo[1.1.1]pentane

There total 4 articles about 1-Bromobicyclo[1.1.1]pentane 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: 2.0%

: 128884-79-7
Bicyclo[1.1.1]pentane-1-carboxylic acid 2-thioxo-2H-pyridin-1-yl ester

: 10555-50-7
1-chlorobicyclo<1.1.1>pentane

: 128884-80-0
1-bromobicyclo<1.1.1>pentane

Guidance literature:: With dmap; 1,1,1-trifluoro-2-bromo-2-chloroethane; for 1h; Heating; Irradiation;

Reference yield:

: 155635-19-1
1-bromo-3-chlorobicyclo<1.1.1>pentane

: 22287-43-0
1,3-dichlorobicyclo<1.1.1>pentane

: 10555-50-7
1-chlorobicyclo<1.1.1>pentane

: 128884-80-0
1-bromobicyclo<1.1.1>pentane

Guidance literature:: With triethylsilane; di-tert-butyl peroxide; at 200 ℃; for 1.5h; Irradiation;

Reference yield:

: 164795-72-6
1-bromo-3-(4,4-dimethyl-2-oxazolinyl)bicyclo<1.1.1>pentane

: 128884-80-0
1-bromobicyclo<1.1.1>pentane

: 1-bromo-3-fluoro-bicyclo<1.1.1>pentane

Guidance literature:: With hydrogenchloride; 1-hydroxy-2(1H)-pyridinethione; 1,1,1-trifluoro-2-bromo-2-chloroethane; tert.-butyl lithium; 2-fluoro-3,3-dimethyl-2,3-dihydro-1,2-benzisothiazole-1,1-dioxide; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;