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249432

Sigma-Aldrich

Undecanoyl chloride

99%

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About This Item

Linear Formula:
CH3(CH2)9COCl
CAS Number:
17746-05-3
Molecular Weight:
204.74
Beilstein:
1759226
EC Number:
241-741-1
MDL number:
MFCD00000739
UNSPSC Code:
12352100
PubChem Substance ID:
24854992
NACRES:
NA.22

Assay

99%

refractive index

n20/D 1.443 (lit.)

bp

135-136 °C/20 mmHg (lit.)

functional group

acyl chloride

SMILES string

CCCCCCCCCCC(Cl)=O

InChI

1S/C11H21ClO/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2-10H2,1H3

InChI key

JUKPJGZUFHCZQI-UHFFFAOYSA-N

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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.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBM2843V
1155866V
053878/2
1155866
07013TY

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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
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)

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