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N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-im-2-chlorotrityl-D-histidine

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Identification

Structural Formula
N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-im-2-chlorotrityl-D-histidine
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Molecular Formula:
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Description

The Clt (2-chlorotrityl) protecting group is more stable than the commonly used Trt group and is being cleaved with 90%TFA and thiol scavengers in dichloromethane. This property makes His(Clt) derivatives useful in the preparation of protected peptide fragments because the Trt-protection is in several cases not completely stable under the conditions required for the cleavage of protected peptides from 2-chlorotrityl resin. References: Aletras A., Barlos K. et al; Int. J. Pept. Protein Res. 1995; 45(5): 488-496. Barlos K. et al; Int. J. Pept. Protein Res. 1991; 38(6): 555-561. Sarah L.M. et al, in „Fmoc Solid Phase Synthesis. A practical approach“, Ed.: Chan W.C., White P.D. Oxford University Press 2000, page 177.


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Iris Biotech GmbH
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Properties for N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-im-2-chlorotrityl-D-histidine

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Alternative Distributors of [N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-im-2-chlorotrityl-D-histidine]

Producers or manufacturers change the product range from time to time. The following companies
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ABCR GmbH & Co. KG

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