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About This Item
Linear Formula:
Br(CH2)8Br
CAS Number:
Molecular Weight:
272.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-912-5
Beilstein/REAXYS Number:
1698114
MDL number:
Assay:
98%
Form:
liquid
InChI key
DKEGCUDAFWNSSO-UHFFFAOYSA-N
InChI
1S/C8H16Br2/c9-7-5-3-1-2-4-6-8-10/h1-8H2
SMILES string
BrCCCCCCCCBr
assay
98%
form
liquid
Quality Level
bp
270-272 °C (lit.)
mp
12-16 °C (lit.)
density
1.477 g/mL at 25 °C (lit.)
Related Categories
General description
1,8-Dibromooctane is primarily used in organic synthesis as a building block for the preparationof various chemical intermediates.It is used as an alkylating reagent in one-pot synthesis for the production of paraffin-like oligomers and it is used to 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
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)
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