8.55098
(3-Formylindolyl)acetamidomethyl polystyrene
Novabiochem®
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
NACRES:
NA.22
UNSPSC Code:
13111023
Product Name
(3-Formylindolyl)acetamidomethyl polystyrene, Novabiochem®
product line
Novabiochem®
form
beads
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
manufacturer/tradename
Novabiochem®
application(s)
peptide synthesis
functional group
aldehyde
storage temp.
2-8°C
Quality Level
Analysis Note
Color (visual): white to yellow to beige
Appearance of substance (visual): beads
Loading (determined by elemental analysis of sulfur after coupling with tosylhydrazide): 0.60 - 1.20 mmol/g
Swelling Volume (in DMF): lot specific result
The polymer matrix is copoly (styrene-1% DVB), 100 - 200 mesh
Appearance of substance (visual): beads
Loading (determined by elemental analysis of sulfur after coupling with tosylhydrazide): 0.60 - 1.20 mmol/g
Swelling Volume (in DMF): lot specific result
The polymer matrix is copoly (styrene-1% DVB), 100 - 200 mesh
General description
Versatile indole-based linker for the synthesis of secondary amides, carbamates, ureas [1,2,3,4] and aminopurines [5]. In a study comparing the cleavage rates of secondary amides, ureas, carbamates and sulfonamides from indole, dialkoxybenzaldehyde and Rink amide resins, the indole resin was found to be the most acid-labile [6].Reductive amination with excess of amine and NaBH(OAc)3 in DCE/TMOF [seepage], NaBH3CN in THF/TMOF/AcOH, or NaBH4-Ti(OiPr)4 in THF [2], converts the formyl group to the appropriate secondary amine. Cleavage can be effected with 2-5% TFA in DCM, depending on the nature of the product being released from the resin.
Associated Protocols and Technical Articles
Protocols for Loading of Peptide Synthesis Resins
Literature references
[1] K. G. Estep, et al. (1998) J. Org. Chem., 63, 5300.
[2] S. Bhattacharyya, et al. (2003) Tetrahedron Lett., 44, 6099.
[3] N. Hone, et al. (2003) Tetrahedron Lett., 44, 8169.
[4] L. Sereni, et al. (2004) Tetrahedron, 60, 8561.
[5] P. H. Dorff and R. S. Garigipati (2001) Tetrahedron Lett., 42, 2771.
[6] B. Yan, et al. (2000) J. Comb. Chem., 2, 66.
Associated Protocols and Technical Articles
Protocols for Loading of Peptide Synthesis Resins
Literature references
[1] K. G. Estep, et al. (1998) J. Org. Chem., 63, 5300.
[2] S. Bhattacharyya, et al. (2003) Tetrahedron Lett., 44, 6099.
[3] N. Hone, et al. (2003) Tetrahedron Lett., 44, 8169.
[4] L. Sereni, et al. (2004) Tetrahedron, 60, 8561.
[5] P. H. Dorff and R. S. Garigipati (2001) Tetrahedron Lett., 42, 2771.
[6] B. Yan, et al. (2000) J. Comb. Chem., 2, 66.
Other Notes
Replaces: 01-64-0361
Legal Information
Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service