511323
Di-tert-butyl iminodiacetate
98%
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About This Item
Linear Formula:
HN[CH2CO2C(CH3)3]2
CAS Number:
Molecular Weight:
245.32
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
InChI
1S/C12H23NO4/c1-11(2,3)16-9(14)7-13-8-10(15)17-12(4,5)6/h13H,7-8H2,1-6H3
SMILES string
CC(C)(C)OC(=O)CNCC(=O)OC(C)(C)C
InChI key
SMXMBXPLRFTROI-UHFFFAOYSA-N
assay
98%
mp
38-42 °C (lit.)
functional group
amine, ester
Quality Level
Related Categories
General description
Di-tert-butyl iminodiacetate is a secondary amine.
Application
Di-tert-butyl iminodiacetate may be used as a reagent in the synthesis of:
- multi-carboxylic acid-containing carbocyanine dyes
- monosubstituted difunctionalized polyhedral oligomeric silsesquioxanes (POSS) monomers
- multigenerational fluorinated dendrimers
- 2,6-dipyrazol-1-ylpyridine derivatives
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
Regulatory Information
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Lanthanide Complexes of Polyacid Ligands derived from 2,6-bis(pyrazol-1-yl) pyridine, pyrazine, and 6,6'-bis(pyrazol-1-yl)-2, 2'-bipyridine: Synthesis and luminescence properties.
Rodriguez-Ubis JC, et al.
Helvetica Chimica Acta, 80(1), 86-96 (1997)
A facile route to difunctionalized monosubstituted octasilsesquioxanes.
Liu H, et al.
Chemistry (Weinheim An Der Bergstrasse, Germany), 17(18), 5019-5023 (2011)
Solid-Supported Synthesis of Bicyclic Peptides Containing Three Parallel Peptide Chains.
Karskela T, et al.
European Journal of Organic Chemistry, 2003(9), 1687-1691 (2003)
Fluorous mixture synthesis of asymmetric dendrimers.
Jiang ZX and Yu YB.
The Journal of Organic Chemistry, 75(6), 2044-2049 (2010)
Yunpeng Ye et al.
Bioconjugate chemistry, 16(1), 51-61 (2005-01-20)
Synergistic multivalent interactions can amplify desired chemical or biological molecular recognitions. We report a new class of multicarboxylate-containing carbocyanine dye constructs for use as optical scaffolds that not only serve as fluorescent antennas but also participate in structural assembly of
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