249432
Undecanoyl chloride
99%
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About This Item
Linear Formula:
CH3(CH2)9COCl
CAS Number:
Molecular Weight:
204.74
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
241-741-1
Beilstein/REAXYS Number:
1759226
MDL number:
Assay:
99%
InChI key
JUKPJGZUFHCZQI-UHFFFAOYSA-N
InChI
1S/C11H21ClO/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2-10H2,1H3
SMILES string
CCCCCCCCCCC(Cl)=O
assay
99%
refractive index
n20/D 1.443 (lit.)
bp
135-136 °C/20 mmHg (lit.)
functional group
acyl chloride
Quality Level
Related Categories
Application
Undecanoyl chloride has been used in the synthesis of:
- chrysotrione B, 2-acylcyclopentene-1,3-dione derivative, isolated from the fruiting bodies of the basidiomycete Hygrophorus chrysodon
- 2-methylpentadecan-5-one
- 4-ketotetradecanoic acid
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
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71. Experiments on the synthesis of carbonyl compounds. Part II. A general synthesis of saturated ketones, R? CO? CH2R'.
Bowman RE.
Journal of the Chemical Society, 325-329 (1950)
Gianluca Gilardoni et al.
Journal of natural products, 70(1), 137-139 (2007-01-27)
Chrysotriones A (1) and B (2), two new 2-acylcyclopentene-1,3-dione derivatives, were isolated from the fruiting bodies of the Basidiomycete Hygrophorus chrysodon, and their structures were established by spectroscopic data and synthesis of compound 2. They represent the first examples of
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