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1-Benzylidene-2-(4-p-tolylthiazol-2-yl)hydrazine is a complex organic compound with the molecular formula C16H14N4S. It is characterized by a benzylidene group (C6H5-CH=) attached to a hydrazine molecule (NH-NH2), with a 4-p-tolylthiazol-2-yl group (C6H4-CH3-S-C2H2N2) connected to the hydrazine's nitrogen atom. 1-benzylidene-2-(4-p-tolylthiazol-2-yl)hydrazine is known for its potential applications in pharmaceuticals and agrochemicals, particularly as an intermediate in the synthesis of various biologically active molecules. Its chemical structure and properties make it a valuable component in the development of new drugs and pesticides.

4871-20-9

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4871-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4871-20-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4871-20:
(6*4)+(5*8)+(4*7)+(3*1)+(2*2)+(1*0)=99
99 % 10 = 9
So 4871-20-9 is a valid CAS Registry Number.

4871-20-9Downstream Products

4871-20-9Relevant academic research and scientific papers

Design, synthesis and biological evaluation of some novel benzylidene-2-(4-phenylthiazol-2-yl) hydrazines as potential anti-inflammatory agents

Bharti, Sanjay Kumar,Singh, Sushil Kumar

, p. 1004 - 1015 (2014/03/21)

A series of substituted benzylidene-2-(4-phenylthiazol-2-yl) hydrazines (2a-q) have been synthesized, characterized and evaluated for their anti-inflammatory activity by carrageenin-induced hind paw edema (acute inflammation) and cotton pellet granuloma (chronic inflammation) methods in rats. In carrageenin-induced hind paw edema method, compounds 2a, 2b, 2c, 2d, 2h, 2k and 2p at a dose of 20 mg kg-1 body weight, p.o. showed excellent inhibitions (51.80-86.74 %) in between 1 and 4 h. Similarly, in cotton pellet granuloma method, compounds 2a, 2b, 2c, 2d, 2h, 2k and 2p at a dose of 20 mg kg-1 body weight, p.o. inhibited the granuloma formation (71.71-90.19 % inhibition) which was comparable to that of standard drug, ibuprofen (90.36 % inhibition of paw volume at 3 h and 94.02 % inhibition of granuloma formation). Structure activity relationship studies showed excellent activity of the compounds containing electron withdrawing group (fluoro, chloro, bromo or nitro) in phenyl ring at C2 and/or C4 position of thiazole ring.

Synthesis of thiazolo[2,3-c]-s-triazoles using poly[(4-diacetoxyiodo) styrene]

Liu, Shi-Juan,Zhang, Ji-Zhen,Tian, Guan-Rong,Liu, Ping

, p. 1753 - 1758 (2007/10/03)

Arenecarbaldehyde-4-arylthiazol-2-ylhydrazones underwent ring closure with poly[(4-diacetoxyiodo)styrene] (PSDIB) to 3,5-diarylthiazolo[2,3-c]-s-triazoles in dichloromethane. Copyright Taylor & Francis, Inc.

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