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5-amino-2-methyl-6-phenylpyridazin-3(2H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126336-94-5

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126336-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126336-94-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,3,3 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 126336-94:
(8*1)+(7*2)+(6*6)+(5*3)+(4*3)+(3*6)+(2*9)+(1*4)=125
125 % 10 = 5
So 126336-94-5 is a valid CAS Registry Number.

126336-94-5Relevant academic research and scientific papers

PYRROLIDINYL UREA, THIOUREA, GUANIDINE AND CYANOGUANIDINE COMPOUNDS AS TRKA KINASE INHIBITORS

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Paragraph 00624, (2014/06/11)

Compounds of Formula (I): or stereoisomers, tautomers, or pharmaceutically acceptable salts, or solvates or prodrugs thereof, where R1, R2, Ra, Rb, Rc, Rd, X, Ring B, and Ring C are as defined herein, and wherein Ring B moiety and the NH-C(=X)-NH moiety are in the trans configuration, are inhibitors of TrkA kinase and are useful in the treatment of diseases which can be treated with a TrkA kinase inhibitor such as pain, cancer, inflammation/inflammatory diseases, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis and pelvic pain syndrome.

Pyridazine derivatives. XXIV. Efficient N-methylation of diversely substituted 3(2H)-pyridazinones using N,N-dimethylformamide dimethylacetal

Sotelo, Eddy,Ravina, Enrique

, p. 1675 - 1680 (2007/10/03)

A series of diversely substituted 3(2H)-pyridazinones were efficiently N-methylated at position 2 by treatment with N,N-dimethylformamide dimethylacetal in DMF.

Synthesis of Aminopyridazines from Azidopyridazines and Tetrazolopyridazines

Kappe, Th.,Pfaffenschlager, A.,Stadlbauer, W.

, p. 666 - 671 (2007/10/02)

Azidopyridazines 3, 4, 24 and tetrazolopyridazines 10, 13, 28 can be converted to the corresponding aminopyridazines, by reaction with triphenylphosphine via phosphazenes and subsequent hydrolysis (Staudinger reaction).

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