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17856

Sigma-Aldrich

N-Fmoc-iminodiacetic acid

≥99.0%

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Empirical Formula (Hill Notation):
C19H17NO6
CAS Number:
112918-82-8
Molecular Weight:
355.34
Beilstein:
7050417
MDL number:
MFCD01321017
UNSPSC Code:
12352106
PubChem Substance ID:
57647683
NACRES:
NA.26

Assay

≥99.0%

mp

213-217 °C

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

OC(=O)CN(CC(O)=O)C(=O)OCC1c2ccccc2-c3ccccc13

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)

InChI key

LNHILYINDTUUMZ-UHFFFAOYSA-N

Other Notes

Reagent to introduce a glycine residue with free N- and C-termini by acylation (the anhydride is formed with TFA)

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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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