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4362-89-4

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4362-89-4 Usage

General Description

2-(1-phenylethylideneamino)guanidine is a chemical compound with the molecular formula C10H13N5. It is a guanidine derivative that is used in the field of medicinal chemistry for its potential pharmacological properties. 2-(1-phenylethylideneamino)guanidine has been studied for its ability to act as an antihypertensive agent by modulating the activity of certain receptors in the body. Additionally, it has also shown potential as an antiarrhythmic agent, making it of interest in the treatment of cardiac conditions. Further research is needed to fully understand the potential therapeutic applications of 2-(1-phenylethylideneamino)guanidine.

Check Digit Verification of cas no

The CAS Registry Mumber 4362-89-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4362-89:
(6*4)+(5*3)+(4*6)+(3*2)+(2*8)+(1*9)=94
94 % 10 = 4
So 4362-89-4 is a valid CAS Registry Number.

4362-89-4SDS

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 Acetophenon-guanylhydrazon

1.2 Other means of identification

Product number -
Other names 2-Phenyl-aethan-2-on-amidino-hydrazon

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:4362-89-4 SDS

4362-89-4Relevant articles and documents

1,1-Diaminoazines as organocatalysts in phospha-Michael addition reactions

Bharatam, Prasad V.,Chourasiya, Sumit S.,Kathuria, Deepika,Wani, Aabid A.

supporting information, p. 11717 - 11720 (2021/11/12)

1,1-Diaminoazines can act as effective organocatalysts for the formation of phosphorus-carbon bonds between biphenylphosphine oxide and an activated alkene (Michael acceptor). These catalysts provide the P-C adducts at a faster rate and with relatively be

New furin inhibitors based on weakly basic amidinohydrazones

Sielaff, Frank,Than, Manuel E.,Bevec, Dorian,Lindberg, Iris,Steinmetzer, Torsten

body text, p. 836 - 840 (2011/02/27)

A novel series of amidinohydrazone-derived furin inhibitors was prepared; the most potent compounds 17 and 21 inhibit furin with Ki values of 0.46 and 0.59 μM, respectively. In contrast to inhibitor 17, which still contains a guanidino residue,

Evaluation of the thiosemicarbazones of some aryl alkyl ketones and related compounds for anticonvulsant activities

Dimmock, J.R.,McColl, J.M.,Wonko, S.L.,Thayer, R.S.,Hancock, D.S.

, p. 529 - 534 (2007/10/02)

The thiosemicarbazone of acetophenone (1a) had been shown previously to afford protection against experimentally-induced seizures.This report describes the systematic chemical modification of 1a and the activities of these analogues in the maximal electro

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