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2-(3-chlorophenyl)ethanimidamide, also known as 3-chlorophenylamidine or phenylchloroguanidine, is a chemical compound with the molecular formula C8H8ClN3. It is a derivative of guanidine and is characterized by the presence of a chlorophenyl group attached to an ethanimidamide moiety. 2-(3-chlorophenyl)ethanimidamide is used in various industrial and pharmaceutical applications, including as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential antimicrobial and antiparasitic properties. However, it is important to note that 2-(3-chlorophenyl)ethanimidamide is known to have some toxicological effects and should be handled with caution.

55154-89-7

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55154-89-7 Usage

Uses

Used in Pharmaceutical Industry:
2-(3-chlorophenyl)ethanimidamide is used as an intermediate in the synthesis of pharmaceuticals for its potential therapeutic applications. It plays a crucial role in the development of new drugs, particularly in the area of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical industry, 2-(3-chlorophenyl)ethanimidamide is utilized as an intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its unique chemical structure contributes to the effectiveness of these products in controlling pests and weeds.
Used in Antimicrobial Applications:
2-(3-chlorophenyl)ethanimidamide has been studied for its potential antimicrobial properties. It can be used as an antimicrobial agent to combat various types of bacteria and other microorganisms, contributing to the development of new antimicrobial drugs and treatments.
Used in Antiparasitic Applications:
2-(3-chlorophenyl)ethanimidamide has also been investigated for its antiparasitic properties. It can be employed as an antiparasitic agent to target and eliminate parasites, which can be beneficial in the treatment of various parasitic infections.
It is important to reiterate that due to the toxicological effects associated with 2-(3-chlorophenyl)ethanimidamide, proper handling and safety measures should be strictly followed during its use in any application.

Check Digit Verification of cas no

The CAS Registry Mumber 55154-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,5 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55154-89:
(7*5)+(6*5)+(5*1)+(4*5)+(3*4)+(2*8)+(1*9)=127
127 % 10 = 7
So 55154-89-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H9ClN2/c9-7-3-1-2-6(4-7)5-8(10)11/h1-4H,5H2,(H3,10,11)

55154-89-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-chlorophenyl)ethanimidamide

1.2 Other means of identification

Product number -
Other names 3-chlorophenylethanamidine

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:55154-89-7 SDS

55154-89-7Relevant academic research and scientific papers

Evolution of anti-HIV drug candidates. Part 1: From α-Anilinophenylacetamide (α-APA) to imidoyl thiourea (ITU)

Ludovici, Donald W.,Kukla, Michael J.,Grous, Philip G.,Krishnan, Suma,Andries, Koen,De Bethune, Marie-Pierre,Azijn, Hilde,Pauwels, Rudi,De Clercq, Erik,Arnold, Edward,Janssen, Paul A.J.

, p. 2225 - 2228 (2007/10/03)

Stemming from work on a previous clinical candidate, loviride, and other α-APA derivatives, a new series of potent non-nucleoside reverse transcriptase inhibitors (NNRTIs) has been synthesized. The ITU analogues, which contain a unique diarylated imidoyl thiourea, are very active in inhibiting both wild-type and clinically important mutant strains of HIV-1.

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