grade
purum
assay
≥97.0% (GC)
refractive index
n20/D 1.454
bp
201 °C (lit.)
density
1.084 g/mL at 25 °C (lit.)
SMILES string
CCCCCCCCCBr
InChI
1S/C9H19Br/c1-2-3-4-5-6-7-8-9-10/h2-9H2,1H3
InChI key
AYMUQTNXKPEMLM-UHFFFAOYSA-N
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General description
1-Bromononane undergoes degradation on refluxing with ethanolic potassium hydroxide.
Application
1-Bromononane was used to quench dianion to synthesize alcohol.
Synthesis of polyacetylenic acids isolated from Nanodea muscosa.
Alves D, et al.
Tetrahedron Letters, 46(50), 8761-8764 (2005)
P Balgavý et al.
General physiology and biophysics, 5(4), 365-370 (1986-08-01)
Interaction of chemical fusogen n-nonyl bromide with a model membrane formed from phosphatidylcholine was studied using 2D-NMR spectra of heavy water and 31P-NMR proton decoupled spectra of the lipid phosphate group in multilamellar lipid dispersions. n-Nonyl bromide was found to
Brianna Vandrey et al.
Current biology : CB, 30(1), 169-175 (2019-12-17)
Episodic memory requires different types of information to be bound together to generate representations of experiences. The lateral entorhinal cortex (LEC) and hippocampus are required for episodic-like memory in rodents [1, 2]. The LEC is critical for integrating spatial and
G Lunn et al.
American Industrial Hygiene Association journal, 52(6), 252-257 (1991-06-01)
Two techniques were investigated for degrading a number of halogenated compounds of commercial and research importance. Reductive dehalogenation with nickel-aluminum alloy in potassium hydroxide solution was used to degrade iodomethane, chloroacetic acid, trichloroacetic acid, 2-chloroethanol, 2-bromoethanol, 2-chloroethylamine, 2-bromoethylamine, 1-bromobutane, 1-iodobutane
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| Y0000786 | 04061837583827 |
| R4033-10MG | 04061836695187 |
| 1605952-25MG | 04061833832806 |
| PHR3235-50MG | 04065267005379 |
| R4033-50MG | 04061836695194 |
| 00390580-25MG | 04061834242598 |
| 536954-5G | 04061835289073 |
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