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Merck

D42607

Sigma-Aldrich

1,8-Dibromooctane

98%

Sinónimos:

Octamethylene dibromide

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About This Item

Fórmula lineal:
Br(CH2)8Br
Número de CAS:
Peso molecular:
272.02
Beilstein/REAXYS Number:
1698114
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

98%

form

liquid

refractive index

n20/D 1.498 (lit.)

bp

270-272 °C (lit.)

mp

12-16 °C (lit.)

density

1.477 g/mL at 25 °C (lit.)

SMILES string

BrCCCCCCCCBr

InChI

1S/C8H16Br2/c9-7-5-3-1-2-4-6-8-10/h1-8H2

InChI key

DKEGCUDAFWNSSO-UHFFFAOYSA-N

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General description

1,8-Dibromooctaneis primarily used in organic synthesis as a building block for the preparationof various chemical intermediates.It is used as an alkylating reagent in aone-pot synthesis for the production of paraffin-like oligomers and it is usedto enhance crystallization and film formation of perovskite.

Application


  • Efficient manual Fmoc solid-phase synthesis of the N-terminal segment of surfactant protein B (SP-B(1-25)).: This study highlights the application of Fmoc-Gly-Wang resin in the synthesis of peptide segments, specifically demonstrating its utility in constructing the N-terminal segment of surfactant protein B (SP-B). The research underscores the resin′s effectiveness in peptide synthesis, emphasizing its role in generating biochemically significant peptides (Ramli et al., 2009).


Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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From N-vinylpyrrolidone anions to modified paraffin-like oligomers via double alkylation with 1, 8-dibromooctane: access to covalent networks and oligomeric amines for dye attachment
Obels, Daniela and Lievenbr{"u}ck, et, al.
Beilstein Journal of Organic Chemistry, 12, 1395-1400 (2016)
Efficiency enhancement in planar CH3NH3PbI3- xClx perovskite solar cells by processing with bidentate halogenated additives
Fu, Guangsheng and Hou, et al.
Solar Energy Materials and Solar Cells, 165, 36-44 (2017)
Enrico Caruso et al.
Bioorganic & medicinal chemistry, 28(21), 115737-115737 (2020-10-17)
A new class of compounds based on the 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene core, known as BODIPYs, has attracted significant attention as photosensitizers suitable for application in photodynamic therapy (PDT), which is a minimally invasive procedure to treat cancer. In PDT the combination of
Kenji Tajima et al.
Biomacromolecules, 21(2), 581-588 (2019-11-22)
Nanofibrillated bacterial cellulose (NFBC) is produced by culturing a cellulose-producing bacterium under agitated aerobic conditions in a carboxymethylcellulose (CMC)-supplemented medium. Detailed structural analyses revealed that NFBC fiber widths varied with the degree of substitution of the CMC used, and zeta
Enrico Caruso et al.
Journal of photochemistry and photobiology. B, Biology, 197, 111548-111548 (2019-07-10)
The visible light combined with photosensitizers (PSs) is exploited in both antitumoral and antimicrobial fields inducing a photo-oxidative stress within the target cells. Among the different PSs, porphyrins belong to the family of the most promising compounds to be used

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