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60547-96-8

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60547-96-8 Usage

Chemical Properties

Tan Solid

Uses

A metabolite of Terazosin (T105000) and a minor metabolite of Prazosin (P702325). Displays high affinity for the α1-Adrenoceptors, important in the treatment of hypertension

Check Digit Verification of cas no

The CAS Registry Mumber 60547-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,5,4 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60547-96:
(7*6)+(6*0)+(5*5)+(4*4)+(3*7)+(2*9)+(1*6)=128
128 % 10 = 8
So 60547-96-8 is a valid CAS Registry Number.

60547-96-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,7-dimethoxyquinazoline-2,4-diamine

1.2 Other means of identification

Product number -
Other names 6,7-Dimethoxy-2,4-quinazolindiamin

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:60547-96-8 SDS

60547-96-8Upstream product

60547-96-8Downstream Products

60547-96-8Relevant articles and documents

Synthesis and identification of the major metabolites of prazosin formed in dog and rat

Althuis,Hess

, p. 146 - 149 (2007/10/05)

The 6 O demethyl and 7 O demethyl analogues of the new antihypertensive drug prazosin [2 [4 (2 furoyl) piperazin 1 yl] 4 amino 6,7 dimethoxyquinazoline hydrochloride] have been unequivocally synthesized via separate ten step reaction sequences starting from isovanillin and vanillin, respectively. The 6 O demethyl derivative was found to be identical with the major prazosin metabolite formed in dog and rat, while the 7 O demethyl derivative was identical with another, less prevalent but significant metabolite. Two minor metabolites of prazosin, 2 (1 piperazinyl) 4 amino 6,7 dimethoxyquinazoline and 2,4 diamino 6,7 dimethoxyquinazoline, are also described. All four metabolites are less potent blood pressure lowering agents in dogs than prazosin but may contribute to its antihypertensive effect, since they account for a major portion of the administered dose.

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