335216-97-2

Basic information

• Product Name: Butanoic acid, 4-[(2-furanylmethyl)amino]-4-oxo-
• Synonyms: N-FURAN-2-YLMETHYL-SUCCINAMIC ACID;4-((furan-2-ylmethyl)amino)-4-oxobutanoic acid
• CAS NO: 335216-97-2
• Molecular Formula: C₉H₁₁NO₄
• Molecular Weight: 197.19
• Mol File: 335216-97-2.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Butanoic acid, 4-[(2-furanylmethyl)amino]-4-oxo-(CAS DataBase Reference)
• NIST Chemistry Reference: Butanoic acid, 4-[(2-furanylmethyl)amino]-4-oxo-(335216-97-2)
• EPA Substance Registry System: Butanoic acid, 4-[(2-furanylmethyl)amino]-4-oxo-(335216-97-2)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 335216-97-2(Hazardous Substances Data)

Upstream product

• 108-30-5 succinic acid anhydride 
• 617-89-0 furan-2-ylmethanamine 

Downstream Products

• 908138-99-8 N-[3-(1-{5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-tetrahydro-furan-2-yl}-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl)-prop-2-ynyl]-N'-furan-2-ylmethyl-succinamide 

Relevant articles and documents

Post-functionalization of an Anderson-type polyoxomolybdate using a metal-free Diels-Alder click reaction

Functionalization and post-functionalization of polyoxometalates (POMs) by organic groups or biological moieties can provide versatile platforms for creating novel functional hybrids with synergetic properties. Such materials can easily be envisioned as having many advanced applications in biology and materials science. Nowadays, the organic groups or biological moieties used for conjugation with POMs, can readily become increasingly complicated in terms of structure, size and properties. Accordingly, a major challenge lies in the development of efficient conjugation methods. In this work, we report our application of metal-free Diels-Alder click reactions under mild conditions to covalently link an Anderson-type polyoxomolybdate with some organic groups or biological moieties possessing complex structures or different properties. High coupling efficiencies and facile purification methods guarantee > 90 % yields. Clearly, this is an ideal methodology for the synthesis of the post-functionalized POM hybrids. With this technology now in hand, finding valuable applications for such post-functionalized POM hybrids will be a highly significant focus of future investigations. Copyright

A new approach to oligonucleotide labelling using Diels-Alder cycloadditions and detection by SERRS

Diels-Alder cycloaddition has been used to add a benzotriazole azo dye to a diene tagged oligonucleotide to generate unique SERRS signals at 10 attomoles.

MAGNETIC PARTICLE CONJUGATES, MICELLES, AND METHODS OF DELIVERING AGENTS

Embodiments of the present disclosure provide for magnetic particle conjugates, methods of making the magnetic particle conjugates, methods of using magnetic particle conjugates, micelles (also referred to as a magnetic composite nanocarrier (MCNC)), methods of making micelles, methods of using micelles, and the like.