17856
N-Fmoc-iminodiacetic acid
≥99.0%
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About This Item
Empirical Formula (Hill Notation):
C19H17NO6
CAS Number:
Molecular Weight:
355.34
UNSPSC Code:
12352106
NACRES:
NA.26
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
7050417
InChI
1S/C19H17NO6/c21-17(22)9-20(10-18(23)24)19(25)26-11-16-14-7-3-1-5-12(14)13-6-2-4-8-15(13)16/h1-8,16H,9-11H2,(H,21,22)(H,23,24)
SMILES string
OC(=O)CN(CC(O)=O)C(=O)OCC1c2ccccc2-c3ccccc13
InChI key
LNHILYINDTUUMZ-UHFFFAOYSA-N
assay
≥99.0%
mp
213-217 °C
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
Other Notes
Reagent to introduce a glycine residue with free N- and C-termini by acylation (the anhydride is formed with TFA)
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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H O Kim et al.
Journal of medicinal chemistry, 37(20), 3373-3382 (1994-09-30)
1,3-Dialkylxanthine analogues containing carboxylic acid and other charged groups on 8-position substituents were synthesized. These derivatives were examined for affinity in radioligand binding assays at rat brain A3 adenosine receptors stably expressed in CHO cells using the new radioligand [125I]AB-MECA
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