49733
Glutaric acid monoethyl ester chloride
≥97.0% (NT)
Synonym(s):
Ethyl 4-(chloroformyl)butyrate, Ethyl 5-chloro-5-oxovalerate, Ethyl glutaryl chloride
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About This Item
Linear Formula:
ClCO(CH2)3COOC2H5
CAS Number:
Molecular Weight:
178.61
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-000-2
Beilstein/REAXYS Number:
1099817
MDL number:
Assay:
≥97.0% (NT)
InChI
1S/C7H11ClO3/c1-2-11-7(10)5-3-4-6(8)9/h2-5H2,1H3
InChI key
KKJAQUGGQMCNJY-UHFFFAOYSA-N
SMILES string
CCOC(=O)CCCC(Cl)=O
assay
≥97.0% (NT)
refractive index
n20/D 1.443
bp
68-70 °C/0.07 mmHg (lit.)
functional group
acyl chloride, ester
storage temp.
2-8°C
Quality Level
Related Categories
General description
Glutaric acid monoethyl ester chloride (ethyl glutaryl chloride) is a higher acyl chloride homolog. Its reaction with calix[4]arene to form ester group-containing calix[4]arenes has been reported.
Application
Glutaric acid monoethyl ester chloride may be used as a reagent during the multi-step synthesis of lipidic aminoalcohol and diamine derivatives.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Synthesis of Several Diester Group-Containing Calix [4] arenes.
Nam KC, et al.
Bull. Korean Chem. Soc., 17(6), 502-506 (1996)
Esther del Olmo et al.
Bioorganic & medicinal chemistry letters, 16(23), 6091-6095 (2006-09-27)
Lymphoproliferation inhibition and cytotoxicity of a number of lipidic aminoacids, aminoalcohols and diamines were evaluated as a preliminary screening to select potential immunomodulators. The four most potent/less toxic compounds were submitted to delayed hypersensibility (DTH) assays to define the best
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