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1H-Imidazole-2-carboxylic acid, 1-methyl-5-nitro-, hydrazide is a complex organic compound with the chemical formula C5H7N5O3. It is derived from the imidazole family, which is a heterocyclic aromatic organic compound containing a benzene ring fused to a two-atom nitrogen-bridged ring. This specific compound features a methyl group at the 1st position, a nitro group at the 5th position, and a hydrazide group attached to the imidazole ring. It is known for its potential applications in pharmaceuticals and chemical research, particularly in the synthesis of various biologically active molecules. Due to its unique structure, it may exhibit specific properties and reactivity, making it a subject of interest for further exploration in the fields of chemistry and biochemistry.

1787-33-3

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1787-33-3 Usage

Structure

1H-Imidazole-2-carboxylic acid, 1-methyl-5-nitro-, hydrazide

Type

Chemical compound

Use in pharmaceutical research

Intermediate in the synthesis of potential drugs

Known properties

Antiprotozoal, antibacterial, potential antitumor and anti-inflammatory properties

Potential applications

Medications to combat parasitic and bacterial infections, antitumor and anti-inflammatory therapies

Importance

A significant chemical in the field of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 1787-33-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,8 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1787-33:
(6*1)+(5*7)+(4*8)+(3*7)+(2*3)+(1*3)=103
103 % 10 = 3
So 1787-33-3 is a valid CAS Registry Number.

1787-33-3Relevant academic research and scientific papers

Synthesis and in vitro antimicrobial evaluation of 5-(1-methyl-5-nitro-2-imidazolyl)-4H-1,2,4-triazoles

Shafiee, Abbas,Sayadi, Abolfazl,Roozbahani, Marjan Hosseini,Foroumadi, Alireza,Kamal, Fatemeh

, p. 495 - 499 (2002)

The increasing clinical importance of drug-resistant pathogens has lent additional urgency to antimicrobial research. Various 5-(1-methyl-5-nitro-2-imidazolyl)-4H-1,2,4-triazoles (4a-6f) were synthesized and tested in vitro for their antibacterial and antifungal activities. Compounds 4a and 4b exhibited significant effects against Bacillus subtilis at MIC ranges of 0.5-1 μg/mL and moderate effects against Staphylococcus aureus.

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