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Benzothieno[2,3-d]pyridazine is a heterocyclic compound characterized by the fusion of a benzene ring, a thiophene ring, and a pyridazine ring. This complex structure is composed of a central pyridazine ring, which is a six-membered aromatic ring containing two nitrogen atoms, flanked by a benzene ring on one side and a thiophene ring, which is a five-membered aromatic ring with one sulfur atom, on the other side. The compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique electronic and steric properties. It is also of interest in materials science for its possible role in the development of new functional materials. The specific properties and reactivity of benzothieno[2,3-d]pyridazine can vary depending on the substituents attached to the ring system, making it a versatile building block in organic synthesis.

244-92-8

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244-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 244-92-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,4 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 244-92:
(5*2)+(4*4)+(3*4)+(2*9)+(1*2)=58
58 % 10 = 8
So 244-92-8 is a valid CAS Registry Number.

244-92-8Relevant academic research and scientific papers

One-pot synthesis of phthalazines and pyridazino-aromatics: A novel strategy for substituted naphthalenes

Kessler, Simon N.,Wegner, Hermann A.

supporting information; experimental part, p. 3268 - 3271 (2012/08/28)

A new one-pot strategy for the synthesis of phthalazines and pyridazino-aromatics starting from aromatic aldehydes has been developed. A variety of substituents ranging from electron withdrawing to donating is tolerated furnishing the desired 1,2-diazine in good to excellent yields. The products have been applied to the bidentate Lewis acid catalyzed inverse electron-demand Diels-Alder (IEDDA) reaction opening a novel two-step entry into substituted naphthalenes, such as Naproxen.

Synthesis and Diels-Alder reactions of the benzo[4,5]thieno [2,3-c]pyrrole ring system

Sha, Chin-Kang,Hsu, Hsi-Yen,Cheng, Su-Ya,Kuo, Yuan-Liang

, p. 1477 - 1481 (2007/10/03)

The first synthesis of the parent compound of the benzo[4,5]thieno[2,3-c]pyrrole ring system and its derivatives, as well as their Diels-Alder reactions with DMAD and N-phenylmaleimide are reported. A new synthesis of the benzo[4,5]thieno[2,3-d]pyridazine ring system is also described.

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