37034-22-3

Basic information

• Product Name: Carbamic acid, [2-(3,4-dihydroxyphenyl)ethyl]-, phenylmethyl ester
• CAS NO: 37034-22-3
• Molecular Formula: C16H17NO4
• Molecular Weight: 287.315
• Mol File: 37034-22-3.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [2-(3,4-dihydroxyphenyl)ethyl]-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [2-(3,4-dihydroxyphenyl)ethyl]-, phenylmethyl ester(37034-22-3)
• EPA Substance Registry System: Carbamic acid, [2-(3,4-dihydroxyphenyl)ethyl]-, phenylmethyl ester(37034-22-3)

Safety Data

• Hazardous Substances Data: 37034-22-3(Hazardous Substances Data)

Upstream product

• 62-31-7 dopamine hydrochloride 
• 501-53-1 benzyl chloroformate 
• 16010-87-0 benzyl (4-Hydroxy-3-methoxyphenethyl)carbamate 
• 51-61-6 dopamine 

Downstream Products

• 1400565-54-9 C₃₀H₅₃N₃O₁₀ 
• 1400565-53-8 C₂₆H₄₅N₃O₈ 
• 1400565-55-0 tert-butyl 2-[2-(4-{2-[2-(3,4-bis{2-[2-(tert-butoxycarbonylamino)ethoxy]ethoxy}phenethylamino)-2-oxoacetamido]ethyl}-2-{2-[2-(tert-butoxycarbonylamino)ethoxy]ethoxy}phenoxy)ethoxy]ethylcarbamate 
• 1400565-56-1 2-(2-(2-(4-(2-(2-(3,4-bis(2,2-dimethyl-4-oxo-3,8,11-trioxa-5-azatridecan-13-yloxy)phenethylamino)-2-oxoacetamido)ethyl)-2-(2,2-dimethyl-4-oxo-3,8,11-trioxa-5-azatridecan-13-yloxy)phenoxy)ethoxy)ethoxy)ethyl tert-butylcarbamate 
• 1400565-52-7 2-(2-(2-(4-(2-(benzyloxycarbonylamino)ethyl)-2-(2,2-dimethyl-4-oxo-3,8,11-trioxa-5-azatridecan-13-yloxy)phenoxy)ethoxy)ethoxy)ethyl tert-butylcarbamate 
• 1400565-51-6 tert-butyl 2-[2-(4-[2-(Benzyloxycarbonylamino)ethyl]-2-{2-[2-(tert-butoxycarbonylamino)ethoxy]ethoxy}phenoxy)ethoxy]ethylcarbamate 
• 48216-85-9 3,4-O-dibenzoyldopamine 
• 48167-07-3 4-(2-aminoethyl)-1,2-phenylene diacetate 

Relevant articles and documents

Effect of enzymatic sulfation on biochemical and pharmacological properties of catecholamines and tyrosine-containing peptides

Substrate specificity of a novel sulfotransferase produced by Eubacterium A-44 isolated from human feces has been studied. Phenolic drugs, catecholamines, were good acceptors of this bacterial enzyme. With regard to dopamine, sulfation mostly occurred at

Synthesis and biological studies of glycosyl dopamine derivatives as potential antiparkinsonian agents

A new approach to deliver dopamine into the central nervous system, based on the use of D-glucose as transportable agent, has been studied. Glycosyl dopamine derivatives bearing the sugar moiety linked to either the amino group or the catechol ring of dopamine through amide, ester or glycosidic bonds were synthesised as potential antiparkinsonian agents. Studies on the binding to dopamine D2 receptor, in vitro stability, and locomotive effect in mice of the synthetic glycoconjugates are reported. Copyright (C) 2000 Elsevier Science Ltd.

O2-Cu2+-ASCORBIC ACID: A NOVEL OXIDATION SYSTEM FOR THE HIGHLY SELECTIVE O-DEALKYLATION OF 2-ALKOXYPHENOLS

The novel oxidation system "O2-Cu2+-ascorbic acid" is a selective reagent for the oxidative O-dealkylation of 2-alkoxyphenols and affords catechols in good yield.KEYWORDS - O-dealkylation; ascorbic acid; copper ion; oxidation; 2-alkoxyphenol; vanillin; dopamine; guaiacol; catechol