6078-07-5

Basic information

• Product Name: 4-hydroxyamphetamine hydrochloride
• Synonyms: 4-hydroxyamphetamine hydrochloride
• CAS NO: 6078-07-5
• Molecular Weight: 0
• Mol File: 6078-07-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 279.2°C at 760 mmHg
• Flash Point: 122.7°C
• Appearance: /
• Vapor Pressure: 0.0024mmHg at 25°C
• CAS DataBase Reference: 4-hydroxyamphetamine hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 4-hydroxyamphetamine hydrochloride(6078-07-5)
• EPA Substance Registry System: 4-hydroxyamphetamine hydrochloride(6078-07-5)

Safety Data

• Hazardous Substances Data: 6078-07-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H13NO.ClH/c1-7(10)6-8-2-4-9(11)5-3-8;/h2-5,7,11H,6,10H2,1H3;1H

Upstream product

• 3706-26-1 1-methyl-2-(p-methoxyphenyl)-ethylamine hydrochloride 

Relevant articles and documents

Nitric oxide donor β2-agonists: Furoxan derivatives containing the fenoterol moiety and related furazans

The structure of fenoterol, a β2-adrenoceptor agonist used in therapy, has been joined with furoxan NO-donor moieties to give new NO-donor β2-agonists. The furazan analogues, devoid of the property to release NO, were also synthesized for comparison. All the compounds retained β2-agonistic activity at micromolar or submicromolar concentration when tested on guinea pig tracheal rings precontracted with carbachol. Among the furoxan derivatives, the NO contribution to trachea relaxation was evident with product 15b at micromolar concentrations. All the new NO-donor hybrids were able to dilate rat aortic strips precontracted with phenylephrine. Both furoxan and furazan derivatives displayed antioxidant activity greater than that of fenoterol.