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4-Phenyl-1H-imidazol-2-amine hydrochloride is a chemical compound with the molecular formula C13H12N3HCl. It is a white to off-white crystalline powder that is soluble in water and various organic solvents. 4-Phenyl-1H-iMidazol-2-aMine hydrochloride is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain antifungal agents and other therapeutic drugs. Its chemical structure consists of a phenyl ring attached to an imidazole ring, with an amine group at the 2-position and a hydrochloride ion attached, which contributes to its acidic properties. The compound is known for its stability and reactivity, making it a valuable building block in the development of new chemical entities with potential therapeutic applications.

6653-43-6

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6653-43-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6653-43-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,5 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6653-43:
(6*6)+(5*6)+(4*5)+(3*3)+(2*4)+(1*3)=106
106 % 10 = 6
So 6653-43-6 is a valid CAS Registry Number.

6653-43-6SDS

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 5-phenyl-1H-imidazol-2-amine,hydrochloride

1.2 Other means of identification

Product number -
Other names 4-Phenyl-1H-imidazol-2-amine hydrochloride

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:6653-43-6 SDS

6653-43-6Relevant academic research and scientific papers

Identification of Anti-Mycobacterial Biofilm Agents Based on the 2-Aminoimidazole Scaffold

Nguyen, T. Vu,Minrovic, Bradley M.,Melander, Roberta J.,Melander, Christian

, p. 927 - 937 (2019/03/26)

Tuberculosis (TB) remains a significant global health problem for which new therapeutic options are sorely needed. The ability of the causative agent, Mycobacterium tuberculosis, to reside within host macrophages and form biofilm-like communities contributes to the persistent and drug-tolerant nature of the disease. Compounds that can prevent or reverse the biofilm-like phenotype have the potential to serve alongside TB antibiotics to overcome this tolerance, and decrease treatment duration. Using Mycobacterium smegmatis as a surrogate organism, we report the identification of two new 2-aminoimidazole compounds that inhibit and disperse mycobacterial biofilms, work synergistically with isoniazid and rifampicin to eradicate preformed M. smegmatis biofilms in vitro, are nontoxic toward Galleria mellonella, and exhibit stability in mouse plasma.

A novel synthesis of the 2-amino-1H-imidazol-4-carbaldehyde derivatives and its application to the efficient synthesis of 2-aminoimidazole alkaloids, oroidin, hymenidin, dispacamide, monobromodispacamide, and ageladine A

Ando, Naoki,Terashima, Shiro

experimental part, p. 6224 - 6237 (2010/09/11)

A novel synthesis of 2-amino-1H-imidazol-4-carbaldehyde derivatives was achieved by the reaction of tert-butoxycarbonylguanidine with 3-bromo-1,1-dimethoxypropan-2-one as a key step. The usefulness of the derivatives as building blocks was proved by accomplishing the efficient synthesis of the representative 2-aminoimidazole alkaloids, oroidin, hymenidin, dispacamide, monobromodispacamide, and ageladine A.

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