N-Boc-3-benzyloxymethyl-L-histidine

Supplier: BACHEM AMERICAS INC

4006621.0005 4006621.0025 4006621.0100

A-1370.0005BAEA 172.71 USD

A-1370.0005BA A-1370.0025BA A-1370.0100BA

N-Boc-3-benzyloxymethyl-L-histidine

N-Boc-3-benzyloxymethyl-L-histidine

The atoms of the imidazole ring of histidine can be numbered in two different ways. Bachem as well as organic chemists designate the position of N-τ as 1 and the position of N-π as 3, whereas biochemists generally number N-π, the nitrogen atom adjacent to the side chain, as 1, and N-τ as 3.

A protected histidine derivative for Boc-SPPS. Boc-His(Bom)-OH can be coupled with minimal concomitant racemization. As the cleavage of His(Bom) yields HCHO as by-product, scavengers reacting with formaldehyde have to be included in the cleavage system.

A protected histidine derivative for Boc-SPPS. Boc-His(Bom)-OH can be coupled with minimal concomitant racemization. As the cleavage of His(Bom) yields HCHO as by-product, scavengers reacting with formaldehyde have to be included in the cleavage system.

Formula: C₁₉H₂₅N₃O₅
Storage Temperature: Freezer

MDL Number: MFCD00043133
CAS Number: 79950-65-5

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