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433993

Sigma-Aldrich

Ethyl 5-(chloromethyl)-2-furancarboxylate

95%

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About This Item

Empirical Formula (Hill Notation):
C8H9ClO3
CAS Number:
Molecular Weight:
188.61
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

95%

form

liquid

refractive index

n20/D 1.511 (lit.)

bp

115 °C/0.015 mmHg (lit.)

density

1.225 g/mL at 25 °C (lit.)

SMILES string

CCOC(=O)c1ccc(CCl)o1

InChI

1S/C8H9ClO3/c1-2-11-8(10)7-4-3-6(5-9)12-7/h3-4H,2,5H2,1H3

InChI key

JBACYJRMCXLIQU-UHFFFAOYSA-N

Application

Ethyl 5-(chloromethyl)-2-furancarboxylate may be employed for the synthesis of a series of novel sulfamide- and urea-based small-molecule antagonists of the protein-protein interaction IL-2/IL-2Rα. It may be employed as starting material for the synthesis of 5-hydroxymethylfuran-2-carboxylic acid.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Nathan D Waal et al.
Bioorganic & medicinal chemistry letters, 15(4), 983-987 (2005-02-03)
The identification, design, and synthesis of a series of novel sulfamide- and urea-based small-molecule antagonists of the protein-protein interaction IL-2/IL-2Ralpha are described. Installation of a furan carboxylic acid fragment onto a low-micromolar sulfamide resulted in a 23-fold improvement in activity
Shintaro Hara et al.
PloS one, 7(7), e41142-e41142 (2012-08-01)
Many investigators have recognised that a significant proportion of environmental bacteria exist in a viable but non-culturable state on agar plates, and some researchers have also noticed that some of such bacteria clearly recover their growth on matrices other than

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