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448729

Sigma-Aldrich

9-Bromo-1-nonanol

95%

Synonym(s):

Nonamethylene bromohydrin

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About This Item

Linear Formula:
Br(CH2)9OH
CAS Number:
Molecular Weight:
223.15
Beilstein/REAXYS Number:
1737525
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

95%

bp

125-126 °C/2 mmHg (lit.)

mp

33-35 °C (lit.)

SMILES string

OCCCCCCCCCBr

InChI

1S/C9H19BrO/c10-8-6-4-2-1-3-5-7-9-11/h11H,1-9H2

InChI key

USJDOLXCPFASNV-UHFFFAOYSA-N

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pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

228.2 °F - closed cup

flash_point_c

109 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Sequential alkynylation of ω-bromoalkyl triflates: facile access to unsymmetrical non-conjugated diynes including precursors to diene.
Armstrong-Chong RJ, et al.
Tetrahedron, 60(45), 10239-10244 (2004)
Synthesis of the diacetylenic phospholipids 1, 2-(10', 12'-heptadecadiynoyl)-sn-glycero-3-phophatidylcholine and 1, 2-(4', 6'-tricosadiynoyl)-sn-glycero-3-phophatidylcholine.
Hennies PT, et al.
Journal of the Brazilian Chemical Society, 12(1), 64-72 (2001)
In vitro enzymatic oxidation of a fluorine-tagged sulfido substrate analogue: a 19F NMR investigation.
Tremblay AE, et al.
Magnetic Resonance in Chemistry, 44(6), 629-632 (2006)
Néstor M Carballeira et al.
Chemistry and physics of lipids, 145(1), 37-44 (2006-11-28)
The first total syntheses for the (Z)-15-methyl-10-hexadecenoic acid and the (Z)-13-methyl-8-tetradecenoic acid were accomplished in seven steps and in 31-32% overall yields. The (trimethylsilyl)acetylene was the key reagent in both syntheses. It is proposed that the best synthetic strategy towards
Highly ion conductive flexible films composed of network polymers based on polymerizable ionic liquids.
Washiro S, et al.
Polymer, 45(5), 1577-1582 (2004)

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