(2R,4S) -Boc-D-Pro (4-N3) -OH

(2R,4S) -Boc-D-Pro (4-N3) -OH is a click chemistry reagent containing an azide[1]. (2R,4S) -Boc-D-Pro (4-N3) -OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.

Product Specifications

CAS Number

[132622-77-6]

UNSPSC

12352005

Hazard Statement

H301-H311-H331-H341

Target

ADC Linker

Type

Reference compound

Related Pathways

Antibody-drug Conjugate/ADC Related

Applications

Cancer-programmed cell death

Field of Research

Others

Assay Protocol

https://www.medchemexpress.com/2r-4s-boc-d-pro-4-n3-oh.html

Solubility

10 mM in DMSO

Smiles

CC(C)(C)OC(N1[C@H](C[C@@H](C1)N=[N+]=[N-])C(O)=O)=O

Molecular Formula

C10H16N4O4

Molecular Weight

256.26

Precautions

P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P403+P233-P405-P501

References & Citations

[1]Gómez-Vidal JA, et al. Potent and selective conformationally restricted neuronal nitric oxide synthase inhibitors. J Med Chem. 2004 Jan 29;47 (3) :703-10.