93148-78-8

Basic information

• Product Name: ethyl 4-(2-Piperidinylethoxy)benzoate
• Synonyms: ethyl 4-(2-Piperidinylethoxy)benzoate
• CAS NO: 93148-78-8
• Molecular Weight: 277.364
• Mol File: 93148-78-8.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: ethyl 4-(2-Piperidinylethoxy)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 4-(2-Piperidinylethoxy)benzoate(93148-78-8)
• EPA Substance Registry System: ethyl 4-(2-Piperidinylethoxy)benzoate(93148-78-8)

Safety Data

• Hazardous Substances Data: 93148-78-8(Hazardous Substances Data)

Upstream product

• 120-47-8 Ethyl 4-hydroxybenzoate 
• 2008-75-5 N-chloroethylpiperidine hydrochloride 
• 1932-03-2 2-(piperidin-4-yl)ethyl chloride 
• 23382-09-4 silicon dioxide hydrate 

Downstream Products

• 223251-13-6 [4-[2-(1-piperidinyl)ethoxy]phenyl]methanol 
• 84449-80-9 4-(2-piperidin-1-ylethoxy)benzoic acid hydrochloride 
• 166975-76-4 4-(2-(piperidin-1-yl)ethoxy)benzoyl chloride 
• 89407-98-7 4-(2-(piperidin-1-yl)-ethoxy)benzoic acid 
• 1260244-32-3 N,N-diethyl-2-({2-[4-(2-piperidin-1-ylethoxy)phenyl]-quinolin-4-yl}oxy)ethanamine 
• 1319210-09-7 2-[4-(2-piperidin-1-ylethoxy)phenyl]quinolin-4-ol 
• 1319210-03-1 N-(2-acetylphenyl)-4-(2-piperidin-1-ylethoxy)benzamide 
• 1174936-40-3 4-(2-(piperidin-1-yl)ethoxy)benzoyl hydrazine 

Relevant articles and documents

SMALL MOLECULE ANTAGONISTS OF SUMO RELATED MODIFICATION OF CRMP2 AND USES THEREOF

This invention is in the field of medicinal chemistry. In particular, the invention relates to a new class of small-molecules having a piperidinyl-benzoimidazole structure which function as antagonists of small ubiquitin like modifier (SUMO) related modification (SUMOylation) of collapsin response mediator protein 2 (CRMP2), and their use as therapeutics for the treatment of voltage gated sodium channel 1.7 (Nav1.7) related itch, anosmia, migraine event, and/or pain (e.g., neuropathic pain).

2,6-Diphenylthiazolo[3,2-b][1,2,4]triazoles as telomeric G-quadruplex stabilizers

The design and synthesis of 2,6-diphenylthiazolo[3,2-b][1,2,4]triazoles characterized by a large aromatic building block bearing cationic side chains are reported. These molecules are evaluated as telomeric G-quadruplex stabilizers and for their selectivi

Process for the synthesis of vinyl sulfoxides

The present invention is directed to a new process for the synthesis of vinyl sulfoxides, in particular diarylvinyl sulfoxides