51513-80-5
51513-80-5
Chemical Structure
6-(N-Boc)caproic acid NHS
- CAS No.: 51513-80-5
- Formula:C15H24N2O6
- Molecular Weight:328.36
IUPAC Name: 2,5-dioxopyrrolidin-1-yl 6-((tert-butoxycarbonyl)amino)hexanoate
InChIKey: TYJPSIQEEXOQLC-UHFFFAOYSA-N
SMILES: O=C(CC1)N(OC(CCCCCNC(OC(C)(C)C)=O)=O)C1=O
Biological Activity: 6-(N-Boc)caproic acid NHS is a protein cross-linking agent.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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6-(N-Boc)caproic acid NHS | 6-(N-Boc)caproic acid NHS is a protein cross-linking agent. | |||||||||||||||||||||
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Boc-N-PEG1-C2-NHS ester | 98.0% | Boc-N-PEG1-C2-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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T-Butoxycarbonyl-PEG1-NHS ester | T-Butoxycarbonyl-PEG1-NHS ester contains a t-boc protecting group and an NHS ester moiety. T-Butoxycarbonyl-PEG1-NHS ester can be used for the modification and labeling of biomolecules. | |||||||||||||||||||||
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2,5-Dioxopyrrolidin-1-yl octanoate (Standard) | ≥98% | 2,5-Dioxopyrrolidin-1-yl octanoate (Standard) is the analytical standard of 2,5-Dioxopyrrolidin-1-yl octanoate. This product is intended for research and analytical applications. | ||||||||||||||||||||
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2,5-Dioxopyrrolidin-1-yl 3-((tert-butoxycarbonyl)amino)propanoate | 98.50% | 2,5-Dioxopyrrolidin-1-yl 3-((tert-butoxycarbonyl)amino)propanoate (Boc-Beta-Ala-OSu) is a PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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6-(N-Trifluoroacetyl)caproic acid NHS | 6-(N-Trifluoroacetyl)caproic acid NHS (TCFS) is a biochemical reagent. | |||||||||||||||||||||
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6-(tert-Butoxy)-6-oxohexanoic NHS ester | 6-(tert-Butoxy)-6-oxohexanoic NHS ester has a t-butyl ester group and an NHS ester moiety. The t-butyl group can be deprotected under acidic conditions. NHS ester can react specifically and efficiently with primary amines such as the side chain of lysine residues or aminosilane-coated surfaces at neutral or slightly basic condition to form a covalent bond. | |||||||||||||||||||||
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10-(tert-Butoxy)-10-oxodecanoic NHS ester | 10-(tert-Butoxy)-10-oxodecanoic NHS ester has a t-butyl ester group and an NHS ester moiety. The t-butyl group can be deprotected under acidic conditions. NHS ester can react specifically and efficiently with primary amines such as the side chain of lysine residues or aminosilane-coated surfaces at neutral or slightly basic condition to form a covalent bond. | |||||||||||||||||||||
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Boc-5-aminopentanoic NHS ester | Boc-5-aminopentanoic NHS ester is a linker containing an NHS ester and a t-Boc protected amine group. The t-Boc group can be deprotected under mild acidic conditions to form a free amine. The NHS ester can be used to label the primary amines (-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules. | |||||||||||||||||||||
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Methyl N-succinimidyl adipate | Methyl N-succinimidyl adipate is a biochemical assay reagent. | |||||||||||||||||||||
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Boc-Gly-Gly-NHS ester | 97.0% | Boc-Gly-Gly-NHS ester can be used to selectively attach small molecules to specific amino acid residues on proteins, creating conjugates that can be used for a variety of applications in drug discovery and diagnostic assays. | ||||||||||||||||||||
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