433993
Ethyl 5-(chloromethyl)-2-furancarboxylate
95%
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About This Item
Empirical Formula (Hill Notation):
C8H9ClO3
CAS Number:
Molecular Weight:
188.61
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
95%
Form:
liquid
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
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Regulatory Information
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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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 433993-5G | 04061837614712 |