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4-amino-N'-((5-nitrofuran-2-yl)methylene)benzohydrazide is a complex organic compound with the chemical formula C11H8N4O4. It is a derivative of benzohydrazide, featuring a 4-amino group and a 5-nitrofuran-2-ylmethylene moiety. 4-amino-N’-((5-nitrofuran-2-yl)methylene)benzohydrazide is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the development of antibiotics and antifungal agents. Its structure allows for the formation of important heterocyclic compounds, which can exhibit significant biological activity. The compound's properties, such as its reactivity and stability, make it a valuable intermediate in the chemical industry for creating new molecules with therapeutic or pesticidal properties.

736-51-6

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736-51-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 736-51-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 736-51:
(5*7)+(4*3)+(3*6)+(2*5)+(1*1)=76
76 % 10 = 6
So 736-51-6 is a valid CAS Registry Number.

736-51-6Downstream Products

736-51-6Relevant academic research and scientific papers

Synthesis and investigation of antimicrobial activity of some nifuroxazide analogues

Alsaeedi, Huda S.,Aljaber, Nabila A.,Ara, Ismet

, p. 3639 - 3646 (2015/12/26)

A series of nifuroxazide analogues [(2a-2e)-(10a-10f)] have been synthesized, structurally identified and tested for antimicrobial activity against a panel of bacteria (Gram-positive and Gram-negative) and the yeast-like pathogenic fungus Candida albicans. The most active compound in this series was 4-amino-benzoic acid (5-nitro-furan-2-ylmethylene)-hydrazide (2b) and 2-amino-benzoic acid (5-nitrofuran-2-ylmethylene)-hydrazide (2d). Furthermore, compounds (9a-9g) and (10a-10g) recorded no activity against selected species except compounds (9f) and (10f) suggesting that using furoic hydrazide and the corresponding hydrazide of thiophene did not improve the antimicrobial activities for this type of compounds. Regarding the activity against Candida albicans, all compounds showed no activity with an exception of substituted nitro furan (2a-2d).

Exploring 5-nitrofuran derivatives against nosocomial pathogens: Synthesis, antimicrobial activity and chemometric analysis

Zorzi, Rodrigo Rocha,Jorge, Salomao Doria,Palace-Berl, Fanny,Pasqualoto, Kerly Fernanda Mesquita,Bortolozzo, Leandro De Sa,De Castro Siqueira, Andre Murillo,Tavares, Leoberto Costa

supporting information, p. 2844 - 2854 (2014/05/06)

The burden of nosocomial or health care-associated infection (HCAI) is increasing worldwide. According to the World Health Organization (WHO), it is several fold higher in low- and middle-income countries. Considering the multidrug-resistant infections, t

Synthesis and biological activity of nifuroxazide and analogs

Tavares,Penna,Amaral

, p. 244 - 249 (2007/10/03)

Nifuroxazide and thirteen analogs were synthesized from substituted benzoic acids and minimal inhibitory concentrations were determined using the serial dilution tests, in three sequential steps. Nifuroxazide and chloramphenicol were used as reference standards. The tests were performed in TSB against the standard bacterial strain of Staphylococcus aureus ATCC 25923.

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