2-Bromo-5-methylfuran

Base Information

Chemical Name:2-Bromo-5-methylfuran
CAS No.:123837-09-2
Molecular Formula:C5H5BrO
Molecular Weight:160.998
Hs Code.:2932190090
Mol file:123837-09-2.mol

Synonyms:2-Bromo-5-methylfuran;

Suppliers and Price of 2-Bromo-5-methylfuran

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

TRC
2-Bromo-5-methylfuran
1g
$ 495.00

TRC
2-Bromo-5-methylfuran
250mg
$ 155.00

SynQuest Laboratories
2-Bromo-5-methylfuran 95%
500 mg
$ 192.00

SynQuest Laboratories
2-Bromo-5-methylfuran 95%
1 g
$ 352.00

SynQuest Laboratories
2-Bromo-5-methylfuran 95%
5 g
$ 1080.00

Labseeker
2-Bromo-5-methylfuran 97
10g
$ 390.00

Biosynth Carbosynth
2-Bromo-5-methylfuran
250 mg
$ 165.00

Biosynth Carbosynth
2-Bromo-5-methylfuran
2 g
$ 850.00

Biosynth Carbosynth
2-Bromo-5-methylfuran
1 g
$ 500.00

Biosynth Carbosynth
2-Bromo-5-methylfuran
100 mg
$ 83.00

Total 44 raw suppliers

Chemical Property of 2-Bromo-5-methylfuran

Chemical Property:

Vapor Pressure:10.8mmHg at 25°C
Refractive Index:1.505
Boiling Point:132.7 °C at 760 mmHg
Flash Point:34 °C
PSA：13.14000
Density:1.537 g/cm³
LogP:2.35050
Storage Temp.:under inert gas (nitrogen or Argon) at 2-8°C

Purity/Quality:

97% ^*data from raw suppliers

2-Bromo-5-methylfuran ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 2-Bromo-5-methylfuran is used as a reagent to synthesize quinuclidine-based ligands, compounds that act as muscarinic agonists.

Technology Process of 2-Bromo-5-methylfuran

There total 5 articles about 2-Bromo-5-methylfuran 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: 60.0%

: 52804-46-3
5-[(tetrahydro-2H-pyran-2-yl)oxy]pent-3-yn-2-one

: 123837-09-2
(5-methylfuran-2-yl)lithium

Guidance literature:: With hydrogen bromide; In pentane; for 2.5h; Ambient temperature;
DOI:10.7164/antibiotics.49.390

Reference yield: 36.0%

: 534-22-5
2-methylfuran

: 123837-09-2
(5-methylfuran-2-yl)lithium

Guidance literature:: With bromine; In N,N-dimethyl-formamide; for 0.5h; Ambient temperature;
DOI:10.1007/BF00810886

Reference yield:

: 41718-86-9
5-bromopenta-3,4-dien-2-one

: 24666-43-1
3-bromo-5-methylfuran

: 123837-09-2
(5-methylfuran-2-yl)lithium

Guidance literature:: gold(III) chloride; In toluene; at 20 ℃; for 0.5h; Further Variations:; Catalysts; Solvents; Reagents; Product distribution;
DOI:10.1021/ja802144t