86359
TentaGel™ S-NH2
extent of labeling: 0.20-0.35 mmol/g N loading
Synonym(s):
O-(2-Aminoethyl)polyethylene glycol polymer-bound
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About This Item
Recommended Products
product line
TentaGel™
form
solid
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
extent of labeling
0.20-0.35 mmol/g N loading
particle size
110-150 μm
application(s)
peptide synthesis
functional group
amine
storage temp.
2-8°C
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Application
TentaGel™ S-NH2 can be used:
- As a support in the synthesis of L-Leu based peptides and oligomers, which are used as catalysts in Julia-Colonna epoxidation of chalcones.
- In the synthesis of 1,3-dialkyl quinazoline-2,4-diones.
- To synthesize N-substituted amidinoaryloxypyridine analogs as potent factor Xa inhibitors.
Legal Information
TentaGel is a trademark of Rapp Polymere GmbH
Storage Class Code
11 - Combustible Solids
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)
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’.
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Find documentation for the products that you have recently purchased in the Document Library.
Highly enantioselective enone epoxidation catalyzed by short solid phase-bound peptides: dominant role of peptide helicity
Berkessel A, et al.
Organic Letters, 3(24), 3839-3842 (2001)
Solid-phase synthesis of 1, 3-dialkyl quinazoline-2, 4-diones
Buckman BO and Mohan R
Tetrahedron Letters, 37(26), 4439-4442 (1996)
Solid-phase synthesis of N-substituted amidinophenoxy pyridines as factor Xa inhibitors
Mohan R, et al.
Bioorganic & Medicinal Chemistry Letters, 8(14), 1877-1882 (1998)
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