76510
Pentadecane
≥98.0% (GC)
Synonym(s):
n-Pentadecane
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25 ML
$54.00
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$148.00
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25 ML
$54.00
100 ML
$148.00
About This Item
Linear Formula:
CH3(CH2)13CH3
CAS Number:
Molecular Weight:
212.41
Beilstein/REAXYS Number:
1698194
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
vapor density
7.4 (vs air)
vapor pressure
1 mmHg ( 91.6 °C)
assay
≥98.0% (GC)
form
liquid
expl. lim.
6.5 %
refractive index
n20/D 1.431 (lit.)
bp
270 °C (lit.)
mp
8-10 °C (lit.)
density
0.769 g/mL at 25 °C (lit.)
SMILES string
CCCCCCCCCCCCCCC
InChI
1S/C15H32/c1-3-5-7-9-11-13-15-14-12-10-8-6-4-2/h3-15H2,1-2H3
InChI key
YCOZIPAWZNQLMR-UHFFFAOYSA-N
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Related Categories
signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1
supp_hazards
Storage Class
10 - Combustible liquids
wgk_germany
WGK 1
flash_point_f
219.2 °F - closed cup
flash_point_c
104 °C - closed cup
ppe
Eyeshields, Gloves
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From 2,2'-methylenedifuran to all stereomeric pentadecane-1,3,5,7,9,11,13,15-octols.
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Conjugate reduction of an enone accompanied by in situ intramolecular aldol condensation was used to construct the tetrasubstituted cyclohexane nucleus of phomactins. Subsequent relay ring-closing metathesis completed the nine-membered ansa bridge of the diterpenoid framework.
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A concise synthesis of the tricyclic furanochroman unit 3 found in the PAF antagonist phomactin A (1) isolated from the marine fungus Phoma sp., is described. In complementary studies, a variety of synthetic routes towards the bicyclo[9.3.1]pentadecane ring system 4
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