251860
1-Iodononane
95%
Synonym(s):
Nonyl iodide
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About This Item
Linear Formula:
CH3(CH2)8I
CAS Number:
Molecular Weight:
254.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
224-286-3
MDL number:
Assay:
95%
Form:
liquid
InChI key
OGSJMFCWOUHXHN-UHFFFAOYSA-N
InChI
1S/C9H19I/c1-2-3-4-5-6-7-8-9-10/h2-9H2,1H3
SMILES string
CCCCCCCCCI
assay
95%
form
liquid
contains
copper as stabilizer
refractive index
n20/D 1.487 (lit.)
bp
107-108 °C/8 mmHg (lit.)
density
1.288 g/mL at 25 °C (lit.)
functional group
alkyl halide, iodo
Quality Level
Related Categories
Application
1-Iodononane has been used in the synthesis of:
- Sch II, a cerebroside that induces fruiting body formation in the basidiomycete Schizophyllum commune
- 2,6-dimethyl-4-nonylpyridine
- 2-tridecanone
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
185.0 °F - closed cup
flash_point_c
85 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Sulfone-mediated synthesis of polysubstituted pyridines.
Craig D and Henry GD.
Tetrahedron Letters, 46(15), 2559-2562 (2005)
Fiona J Black et al.
Organic & biomolecular chemistry, 8(5), 1188-1193 (2010-02-19)
(4E,8E,10E)-9-Methyl-4,8,10-sphingatrienine, a core component of marine sphingolipids, was synthesised for the first time using a copper(I)-mediated 1,2-metallate rearrangement of a lithiated glycal as a key step. It was converted to phalluside-1, a cerebroside isolated from the ascidian Phallusia fumigate. By
Ultrasound mediated synthesis of a few naturally occurring compounds.
Singh J, et al.
Indian J. Chem. B, 40(5), 386-390 (2005)
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