163070-77-7

Basic information

• Product Name: 8-<4-(2-Hydroxyethyl)phenyl>naphthalin-1-carboxamidoxim
• Synonyms: 8-<4-(2-Hydroxyethyl)phenyl>naphthalin-1-carboxamidoxim
• CAS NO: 163070-77-7
• Molecular Weight: 306.364
• Mol File: 163070-77-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 8-<4-(2-Hydroxyethyl)phenyl>naphthalin-1-carboxamidoxim(CAS DataBase Reference)
• NIST Chemistry Reference: 8-<4-(2-Hydroxyethyl)phenyl>naphthalin-1-carboxamidoxim(163070-77-7)
• EPA Substance Registry System: 8-<4-(2-Hydroxyethyl)phenyl>naphthalin-1-carboxamidoxim(163070-77-7)

Safety Data

• Hazardous Substances Data: 163070-77-7(Hazardous Substances Data)

Upstream product

• 163070-73-3 (RS)-<2-(4-Iodphenyl)ethyl>ether 
• 163070-75-5 8-{4-[2-(Tetrahydro-pyran-2-yloxy)-ethyl]-phenyl}-naphthalene-1-carbonitrile 
• 157735-55-2 8-Iodnaphthalin-1-carboxamid 
• 157735-41-6 8-iodonaphthalene-1-carbonitrile 
• 13577-19-0 8-iodo-1-naphthoic acid 
• 1798-06-7 (4-iodophenyl)acetic acid 
• 52914-23-5 4-iodophenethyl alcohol 
• 163070-76-6 8-<4-(2-Hydroxyethyl)phenyl>naphthalin-1-carbonitril 

Relevant articles and documents

Supramolecular Phosphoryl Transfer Reactions Mediated by Amidinium Phosphate Ion-Pair Complexes

In order to build up simplified synthetic models of staphylococcal nuclease two derivatives of 8-phenylnaphthalene-1-carboxamidine equipped with nucleophilic side chains have been prepared (1, 2).After protonation these amidinium alcohols bind phosphodiester anions via hydrogen bonds and react within the ion-pair complexes to give zwitterionic products 27 and 28.The rate accelerations (DMF, 30 deg C) compared to the phosphorylation of noncharged alcohols are 2700-fold (2) and 930-fold (1). - Key Words: Artificial phosphodiesterase / Naphthalene, 1,8-disubstituted / Molecular Recognition / Staphylococcal nuclease, model of / Enzymes / Amidinium phosphate / Ion-Pair Complexes / Guanidine