767212
Polyester bis-MPA dendron, 4 hydroxyl, 1 azide
generation 2, 95%
Synonym(s):
bisMPA dendrimer, bisMPA dendron
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About This Item
CAS Number:
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
MDL number:
InChI
1S/C21H37N3O10/c1-19(10-25,11-26)16(29)33-14-21(3,15-34-17(30)20(2,12-27)13-28)18(31)32-9-7-5-4-6-8-23-24-22/h25-28H,4-15H2,1-3H3
SMILES string
CC(CO)(CO)C(=O)OCC(C)(COC(=O)C(C)(CO)CO)C(=O)OCCCCCCN=[N+]=[N-]
InChI key
LGPUUVBKCMNFLE-UHFFFAOYSA-N
description
hydroxyl surface groups
assay
95%
form
solid
mol wt
generation 2
feature
focal point azide
no. Surface Groups
4
mp
93-98 °C (decomposition)
storage temp.
−20°C
General description
Dendrimers and dendrons are symmetrically branched polymer structures that possess a well-defined spatial distribution of functional groups. The properties of dendrimers are steered by controlling the generation number, repeating unit, end groups. hydrophilicity/hydrophobicity are controlled by the functionality of the end groups.
Application
These form extremely attractive molecular targets. Nanotechnological applications range from microelectronics to biomedical devices.2 Other proposed applications are:
- coatings
- resins
- additives,
- analytical techniques
- medicine
- drug and dye delivery
- molecular imprinting
- organic polymer synthesis
- catalysis
- optoelectronic applications.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Per Antoni et al.
Chemical communications (Cambridge, England), (22), 2249-2251 (2007-05-31)
A chemoselective and layered growth approach has been developed for the synthesis of dendrimers, combining Click chemistry with traditional esterification/etherification reactions, without the need for activation steps and with excellent overall yields.
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