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91457-54-4

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91457-54-4 Usage

Type of compound

Organic compound

Derivative

Acetamidine

Usage

Antifungal and antimicrobial agent

Effective against

Skin infections (e.g., athlete's foot, ringworm) and yeast infections

Mechanism of action

Disrupts growth and reproduction of microorganisms

Potential uses

Treating eye infections, preservative in contact lens solutions

Precaution

Use under guidance of a healthcare professional to avoid adverse effects and resistance development

Check Digit Verification of cas no

The CAS Registry Mumber 91457-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,4,5 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91457-54:
(7*9)+(6*1)+(5*4)+(4*5)+(3*7)+(2*5)+(1*4)=144
144 % 10 = 4
So 91457-54-4 is a valid CAS Registry Number.

91457-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,6-dichlorophenyl)-N-(N'-propylcarbamimidoyl)acetamide

1.2 Other means of identification

Product number -
Other names 1-(2,6-Dichlorophenylacetyl)-3-n-propylguanidine

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:91457-54-4 SDS

91457-54-4Downstream Products

91457-54-4Relevant articles and documents

Substituted phenylacetylguanidines: a new class of antihypertensive agents

Bream,Lauener,Picard,Scholtysik,White

, p. 1477 - 1482 (2007/10/05)

The synthesis of a new series of phenylacetylguanidines is described. Several of them exhibited high antihypertensive activity in the rat. The most potent member of the series is N amidino 2 (2,6 dichlorophenyl) acetamide hydrochloride [2,6 dichlorophenylacetylguanidine hydrochloride, compound 19], which is now in clinical study under the clinical code number BS 100-141. The structure activity relationships in this class of compounds are discussed.

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