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90585-97-0

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90585-97-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90585-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,8 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90585-97:
(7*9)+(6*0)+(5*5)+(4*8)+(3*5)+(2*9)+(1*7)=160
160 % 10 = 0
So 90585-97-0 is a valid CAS Registry Number.

90585-97-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-pyrimidin-2-ylguanidine

1.2 Other means of identification

Product number -
Other names 1-(Pyrimidin-2-yl)guanidine

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:90585-97-0 SDS

90585-97-0Upstream product

90585-97-0Downstream Products

90585-97-0Relevant articles and documents

Cardiovascular activity of aromatic guanidine compounds.

Hughes et al.

, p. 1077,1080 (2007/10/04)

A series of aromatic guanidines and several 1-phenylbiguanides was prepared and tested for cardiovascular (CV) effects in anesthetized dogs measuring heart rate, blood pressure, carotid artery blood flow, and myocardial force changes. The predominant CV effect at minimally effective dose was vasoconstriction unassociated with cardiac stimulation. The structure-activity relationships of the compounds were discussed comparing their structural similarities to the beta-phenylethylamines. The most potent members of the series were phenylguanidines substituted in the 3 and 4 positions on the aromatic nucleus with hydroxy or chloro groups. Preliminary mechanism studies indicated that the 3,4-dihydroxyphenylguanidines act at least partially by a direct alpha-adrenergic mechanism

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