900613
5-(4-(4-(Prop-2-yn-1-yloxy)benzoyl)phenoxy)pentanoic acid
≥95%
Synonym(s):
Carboxyl benzophenone alkyne, Probe building block
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About This Item
Empirical Formula (Hill Notation):
C21H20O5
CAS Number:
Molecular Weight:
352.38
MDL number:
UNSPSC Code:
12352106
NACRES:
NA.22
Assay:
≥95%
Form:
solid
Quality Level
assay
≥95%
form
solid
reaction suitability
reaction type: click chemistry
storage temp.
−20°C
SMILES string
O(CCCCC(=O)O)c1ccc(cc1)C(=O)c2ccc(cc2)OCC#C
InChI
1S/C21H20O5/c1-2-14-25-18-10-6-16(7-11-18)21(24)17-8-12-19(13-9-17)26-15-4-3-5-20(22)23/h1,6-13H,3-5,14-15H2,(H,22,23)
InChI key
PVDBYWSDYKTIBJ-UHFFFAOYSA-N
Application
5-(4-(4-(Prop-2-yn-1-yloxy)benzoyl)phenoxy)pentanoic acid is used for chemical probe synthesis, this trifunctional building block contains a light-activated benzophenone, alkyne tag, and carboxylic acid synthetic handle. When appended to a ligand or pharmacophore through its acid linker, this building block allows for UV light-induced covalent modification of a biological target with potential for downstream applications via the alkyne tag. Use alone or in parallel with other multi-functional building blocks to discover the optimal probe for your chemical biology experiments.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Articles
In partnership with Pfizer chemists, we have compiled a collection of trifunctional building blocks to enable development of probes.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 900613-50MG | 04061833250532 |