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6-methyl-5-(4-nitro-styryl)-[1,2,4]triazin-3-ylamine is a complex organic chemical compound with the molecular formula C11H9N5O2. It is characterized by a triazine ring system, which is a six-membered aromatic ring containing three nitrogen atoms. The compound features a methyl group at the 6-position, a 4-nitro-styryl group at the 5-position, and an amine group at the 3-position. The 4-nitro-styryl group consists of a nitro group (-NO2) attached to a styrene moiety, which is a vinylbenzene structure. 6-methyl-5-(4-nitro-styryl)-[1,2,4]triazin-3-ylamine is likely to be used in the synthesis of various pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique structure and reactivity. It is important to handle such compounds with care, as they may have potential health and environmental impacts, and their use is typically restricted to controlled laboratory settings or industrial applications.

1789-25-9

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1789-25-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1789-25-9 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 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1789-25:
(6*1)+(5*7)+(4*8)+(3*9)+(2*2)+(1*5)=109
109 % 10 = 9
So 1789-25-9 is a valid CAS Registry Number.

1789-25-9Downstream Products

1789-25-9Relevant academic research and scientific papers

Synthesis of heterobicyclic nitrogen systems bearing the 1,2,4-triazine moiety as anti-HIV and anticancer drugs: Part I

Abdel-Rahman, Reda M.,Morsy,Hanafy,Amene

, p. 347 - 351 (2007/10/03)

Some new heterobicyclic nitrogen systems bearing the 1,2,4-triazine moiety (3-22) have been achieved by treatment of 3-amino-5,6-disubstituted- 1,2,4-triazines 2a-h with some cyclic and acyclic oxygen compounds followed by heterocyclization. Structures of the products have been deduced by elemental analysis and spectral data. Significant anti-HIV and anticancer activities were observed in vitro for some members of the series, where compounds 5 and 18 showed a moderate activity.

Reaction of 3-Amino-5,6-dimethyl-1,2,4-triazine with Electrophiles

Suzuki, Toshinobu,Okazaki, Masahiko,Mitsuhashi, Keiryo

, p. 935 - 939 (2007/10/02)

The title compound was reacted with four types of electrophiles and the respective reaction sites were investigated.The reaction with aryl isocyanates in the conventional way yielded the corresponding ureas.In the presence of triethylamine, the 3-amino gr

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