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| BCN-succinimidyl ester Basic information |
| Product Name: | BCN-succinimidyl ester | | Synonyms: | (1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethyl N-succinimidyl carbonate;BCN-NHS;BCN-succinimidyl ester;N-[((1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-yl)methyloxycarbonyloxy]succinimide;12-Oxo-5,8-dioxa-2,11-diazahexadecanedioic acid 1-[(1R,8S,9s)-bicyclo[6.1.0]non-4-yn-9-ylmethyl] 16-(2,5-dioxo-1-pyrrolidinyl) ester;2,5-Dioxopyrrolidin-1-yl 1-[(1R,8S,9s)-bicyclo[6.1.0]non-4-yn-9-yl]-3,14-dioxo-2,7,10-trioxa-4,13-diazaoctadecan-18-oate;BCN-POE3-NH-C(O)CH2CH2CH2C(O)OSu;(1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethyl N-succinimidyl carbonate for Copper-free Click Chemistry | | CAS: | 1516551-46-4 | | MF: | | MW: | 0 | | EINECS: | | Product Categories: | | Mol File: | Mol File |
| BCN-succinimidyl ester Chemical Properties |
| BCN-succinimidyl ester Usage And Synthesis |
| Uses | (1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethyl N-succinimidyl carbonate may be used to functionalize the primary amines of the lysine residue of recombinant elastin-like proteins (ELPs). These functionalized ELPs quickly undergo cross-linking via bio-orthogonal strain-promoted azide-alkyne cycloaddition reactions to form hydrogels with high gelation kinetics and tunable mechanics, making them useful biomaterials for cell encapsulation.{67It may also be used to synthesize bicyclononyne functionalized poly(ethylene glycol) polymer coatings with anti-fouling properties towards protein adhesion and cell adhesion for supramolecular ureidopyrimidinone (UPy) based materials. |
| BCN-succinimidyl ester Preparation Products And Raw materials |
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