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N-[3-(carbamothioylamino)phenyl]acetamide is a chemical compound with the molecular formula C9H10N2OS. It is an organic compound that belongs to the class of acetamide derivatives, characterized by the presence of an amide group (-CONH2) attached to a phenyl ring. The compound features a carbamothioyl group (-C(O)NH-CS) connected to the phenyl ring at the 3-position, which imparts unique chemical properties and reactivity. N-[3-(carbamothioylamino)phenyl]acetamide may have potential applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its structural features. However, it is important to note that the specific uses and safety profile of N-[3-(carbamothioylamino)phenyl]acetamide would require further investigation and characterization.

1614-34-2

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1614-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1614-34-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1614-34:
(6*1)+(5*6)+(4*1)+(3*4)+(2*3)+(1*4)=62
62 % 10 = 2
So 1614-34-2 is a valid CAS Registry Number.

1614-34-2Downstream Products

1614-34-2Relevant academic research and scientific papers

Synthesis and in-vitro evaluation of 2-amino-4-arylthiazole as inhibitor of 3D polymerase against foot-and-mouth disease (FMD)

Jeong, Kwi-Wan,Lee, Jung-Hun,Park, Sun-Mi,Choi, Joo-Hyung,Jeong, Dae-Youn,Choi, Dong-Hwa,Nam, Yeonju,Park, Jong-Hyeon,Lee, Kwang-Nyeong,Kim, Su-Mi,Ku, Jin-Mo

, p. 387 - 397 (2015/09/01)

Foot-and-mouth disease (FMD) is a highly contagious vesicular disease of livestock caused by a highly variable RNA virus, foot-and-mouth disease virus (FMDV). One of the targets to suppress expansion of and to control FMD is 3D polymerase (FMDV 3Dpol). In this study, 2-amino-4-arylthiazole derivatives were synthesized and evaluated for their inhibitory activity against FMDV 3Dpol. Among them, compound 20i exhibited the most potent functional inhibition (IC50 = 0.39μM) of FMDV 3D polymerase and compound 24a (EC50=13.09 μM) showed more potent antiviral activity than ribavirin (EC50=1367 μM) and T1105 (EC50=347 μM) with IBRS-2 cells infected by the FMDV O/SKR/2010 strain.

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