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876-26-6 Usage

Uses

p-Hydroxyamphetamine is a major metabolite of Amphetamine (A634240), a sympathomimetic and psychotropic drug which is extensively metabolized in liver and in brain.

Hazard

A reproductive hazard.

Check Digit Verification of cas no

The CAS Registry Mumber 876-26-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 876-26:
(5*8)+(4*7)+(3*6)+(2*2)+(1*6)=96
96 % 10 = 6
So 876-26-6 is a valid CAS Registry Number.

876-26-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	4-(2-aminopropyl)phenol,hydrochloride

1.2 Other means of identification

Product number	-
Other names	4-(2-Aminopropyl)phenol hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:876-26-6 SDS

876-26-6Upstream product

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

876-26-6Downstream Products

876-26-6Relevant articles and documents

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

Federica Buonsanti,Bertinaria, Massimo,Di Stilo, Antonella,Cena, Clara,Fruttero, Roberta,Gasco, Alberto

, p. 5003 - 5011 (2008/03/12)

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.

CAS

876-26-6