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1-((5-Nitrofuran-2-yl)methylene)-4-phenylthiosemicarbazone is a complex organic compound with the molecular formula C11H9N5O2S2. It is characterized by a thiosemicarbazone structure, which is a derivative of the semicarbazone class of compounds. The molecule features a 5-nitrofuran-2-yl group, which is a heterocyclic ring system with a nitro group, and a phenyl ring, which is a benzene ring. 1-((5-nitrofuran-2-yl)methylene)-4-phenylthiosemicarbazone is known for its potential applications in pharmaceutical research, particularly as an antimicrobial agent. Its chemical structure and properties make it a subject of interest in the development of new drugs and therapeutics.

736-52-7

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736-52-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 736-52-7 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 736-52:
(5*7)+(4*3)+(3*6)+(2*5)+(1*2)=77
77 % 10 = 7
So 736-52-7 is a valid CAS Registry Number.

736-52-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-((5-nitrofuran-2-yl)methylene)-4-phenylthiosemicarbazone

1.2 Other means of identification

Product number -
Other names 1-(5-Nitro-2-furfuryliden)-4-phenyl-thiosemicarbazon

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 -
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More Details:736-52-7 SDS

736-52-7Relevant academic research and scientific papers

Tricarbonyl 99mTc(i) and Re(i)-thiosemicarbazone complexes: synthesis, characterization and biological evaluation for targeting bacterial infection

Nayak, Dipak Kumar,Baishya, Rinku,Natarajan, Ramalingam,Sen, Tuhinadri,Debnath, Mita Chatterjee

, p. 16136 - 16148 (2015)

Methyl, ethyl and phenyl nitrofuryl thiosemicarbazone ligands (1, 2 and 3 respectively) were radiolabeled with freshly prepared aqueous solution of a fac[99mTc(CO)3(H2O)3]+ precursor. The radiochemica

Synthesis and evaluation of thiosemicarbazones functionalized with furyl moieties as new chemosensors for anion recognition

Santos-Figueroa, Luis E.,Moragues, María E.,Raposo, M. Manuela M.,Batista, Rosa M. F.,Costa, Susana P. G.,Ferreira, R. Cristina M.,Sancenón, Félix,Martínez-Má?ez, Ramón,Ros-Lis, José Vicente,Soto, Juan

experimental part, p. 7418 - 7428 (2012/09/25)

A family of heterocyclic thiosemicarbazone dyes (3a-f and 4) containing furyl groups was synthesized in good yields, characterized and their response in acetonitrile in the presence of selected anions was studied. Acetonitrile solutions of 3a-f and 4 show

5-Nitrofuran-2-yl derivatives: Synthesis and inhibitory activities against growing and dormant mycobacterium species

Sriram, Dharmarajan,Yogeeswari, Perumal,Dhakla, Prathiba,Senthilkumar, Palaniappan,Banerjee, Debjani,Manjashetty, Thimmappa H.

body text, p. 1152 - 1154 (2009/08/07)

Eighteen 5-nitrofuran-2-yl derivatives were prepared by reacting 5-nitro-2-furfural with various (sub)phenyl/pyridyl thiosemicarbazide using microwave irradiation. The compounds were tested for their in vitro activity against tubercular and various non-tubercular mycobacterium species in log-phase and 6-week-starved cultures. Compound N-(3,5-dibromopyridin-2-yl)-2-((5-nitrofuran-2-yl)methylene)hydrazinecarbothioamide (4r) was found to be the most potent compound (MIC: 0.22 μM) and was 3 times more active than standard isoniazid (INH) and equally active as rifampicin (RIF) in log-phase culture of Mycobacterium tuberculosis H37Rv. In starved M. tuberculosis H37Rv, 4r inhibited with MIC of 13.9 μM and was found to be 50 times more active than INH and slightly more active than RIF.

Synthesis and antimicrobial activity of some 2,5-disubstituted 1,3,4-thiadiazole derivatives

Mamolo,Vio,Banfi

, p. 71 - 74 (2007/10/03)

A series of 5-substituted 2-arylamino-1,3,4-thiadiazole derivatives was prepared. The antimicrobial activity of these compounds against some strains of bacteria and a strain of Candida albicans was determined, together with that of the corresponding thiosemicarbazone derivatives, which are intermediates in the synthetical procedure.

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