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8-chloro-3,4-diphenylpyrimido[4',5':4,5]thieno[2,3-c]pyridazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

189894-90-4

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189894-90-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 189894-90-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,8,9 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 189894-90:
(8*1)+(7*8)+(6*9)+(5*8)+(4*9)+(3*4)+(2*9)+(1*0)=224
224 % 10 = 4
So 189894-90-4 is a valid CAS Registry Number.

189894-90-4Relevant academic research and scientific papers

Pyridazine and its related compounds. Part 36. Synthesis and antimicrobial activity of some novel pyrimido[4′,5′:4,5]thieno[2,3-c]pyridazine derivatives

Deeb, Ali,Mahgoub, Sebaey

, p. 4559 - 4569 (2016/02/20)

Novel derivatives of pyrimidothienopyridazine were designed and synthesized through a versatile method. Some of the target compounds bearing the sulfonamide group were evaluated for their antimicrobial activity against representative Gram-positive bacteria, Gram-negative bacteria, and fungi by applying the agar plate diffusion technique. The results showed that derivatives 11a have promising inhibitory activity against Gram-positive bacteria, and derivatives 11b and 11e have also potent inhibition against fungi. Rest of the compounds showed moderate to low activity against the examined micro-organisms.

Synthesis and reactions of some new heterocyclic compounds containing thieno[2,3-c] pyridazine moiety

Radwan

, p. 153 - 169 (2007/10/03)

Saponification of ethyl 3-amino-4,5-diphenylthieno[2,3-c]pyridazine-2-carboxyate (1) with alcoholic sodium hydroxide, followed by acidification, afforded the corresponding acid 2. Also, reaction of 1 with ethanolamine and formamide, respectively, gave compounds 5 and 6. Compound 2 reacts with orthophosphoric acid under different conditions to give some new thieno[2,3-c] pyridazine derivatives 3 and 4, which were subjected to reactions to produce compounds 7-18. Furtheremore, compounds 5 and 6 were used to synthesize some substituted pyrimido[4′,5′:4,5)-thieno[2,3-c]pyridazine derivatives 21-30.

Synthesis of New Pyridazino[4′,3′:4,5]-thieno[3,2-d]-1,2,3-triazine and Pyrimido [4′,5′:4,5]thieno[2,3-c]pyridazine Derivatives

Quintela,Veiga,Alvarez-Sarandes,Gonzalez,Peinador

, p. 1037 - 1043 (2007/10/03)

8,9-Diphenylpyridazino[4′,3′:4,5]thieno[3,2-d]-1,2,3-triazin- 4(3H)-one (2), 3-substituted 8,9-diphenylpyridazino[4′,3′:4,5]thieno[3,2-d]-1,2,3-triazin-4(3H)- ones (3a-c), 3,4-diphenylpyrimido-[4′,5′:4,5]thieno[2,3-c]pyridazin-8(7H)-one (4), 8-chloro-3,4-diphenylpyrimido[4′,5′:4,5]thieno[2,3-c]pyridazine (5), 8-substituted 3,4-diphenylpyrimido[4′,5′:4,5]thieno[2,3-c]pyridazines (6a-h) and 7-substituted 3,4-diphenylpyrimido[4′,5′:4,5]thieno[2,3-c]pyridazin-8(7H)-ones(7a- c) were synthesized from 5-amino-3,4-diphenylthieno[2,3-c]pyridazine-6-carboxamide (1).

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