345310-96-5

Basic information

• Product Name: Acetamide, 2-[(2-hydroxyethyl)amino]-N-2-pyridinyl- (9CI)
• Synonyms: Acetamide, 2-[(2-hydroxyethyl)amino]-N-2-pyridinyl- (9CI);2-(2-hydroxyethylamino)-N-(pyridin-2-yl)acetamide
• CAS NO: 345310-96-5
• Molecular Formula: C9H13N3O2
• Molecular Weight: 195.21842
• Product Categories: PYRIDINE
• Mol File: 345310-96-5.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Acetamide, 2-[(2-hydroxyethyl)amino]-N-2-pyridinyl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, 2-[(2-hydroxyethyl)amino]-N-2-pyridinyl- (9CI)(345310-96-5)
• EPA Substance Registry System: Acetamide, 2-[(2-hydroxyethyl)amino]-N-2-pyridinyl- (9CI)(345310-96-5)

Safety Data

• Hazardous Substances Data: 345310-96-5(Hazardous Substances Data)

Upstream product

• 504-29-0 2-aminopyridine 
• 141-43-5 ethanolamine 
• 5221-37-4 2-chloro-N-pyridin-2-ylacetamide 

Downstream Products

• 345310-98-7 1-(2-pyridyl)piperazin-2-one 

Relevant articles and documents

Sequence-Defined Dithiocarbamate Oligomers via a Scalable, Support-free, Iterative Strategy

Precise control over the monomeric sequence on natural sequence-defined polymers (SDPs) leads to their structural diversity and functions. However, absolute control over the monomeric sequence on a synthetic polymer remains a challenging process. Herein, we describe a support-free, protection-deprotection-free, cost-effective, and fast iterative strategy for multigram production of a new class of SDP with a unique functional group, dithiocarbamate, a potential group for material and biomedical applications. The strategy is based on a unique monomer, named as amine-hydroxyl monomer, and a three-component reaction between the monomer, CS2, and terminal chloro group of the growing chain. The fast strategy allows us to synthesize a 5-mer sequence-defined oligomer in 6 h. For a proof of concept, a range of aliphatic and aromatic groups have been incorporated at different sequences in the sequence-defined oligomer. This SDP platform has further been advanced by two ways: (i) multiple approaches for postsynthetic modification of SDP and (ii) increasing the chain length in a single step.