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Methanimidamide, N,N-dimethyl-N-1H-pyrazol-3-yl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

266993-91-3

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266993-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 266993-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,6,9,9 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 266993-91:
(8*2)+(7*6)+(6*6)+(5*9)+(4*9)+(3*3)+(2*9)+(1*1)=203
203 % 10 = 3
So 266993-91-3 is a valid CAS Registry Number.

266993-91-3Downstream Products

266993-91-3Relevant academic research and scientific papers

BENZENE SULFONAMIDES AS CCR9 INHIBITORS

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Page/Page column 79; 80, (2015/07/15)

The present invention relates to compounds useful as CCR9 modulators, to compositions containing them, to methods of making them, and to methods of using them. In particular, the present invention relates to compounds capable of modulating the function of the CCR9 receptor by acting as partial agonists, antagonists or inverse agonists. Such compounds may be useful to treat, prevent or ameliorate a disease or condition associated with CCR9 activation, including inflammatory and immune disorder diseases or conditions such as inflammatory bowel diseases (IBD).

Recognition of CG interrupting site by W-shaped nucleoside analogs (WNA) having the pyrazole ring in an anti-parallel triplex DNA

Taniguchi, Yosuke,Uchida, Yuko,Takaki, Tomoko,Aoki, Eriko,Sasaki, Shigeki

experimental part, p. 6803 - 6810 (2010/02/28)

We have previously developed W-shaped nucleoside analogs (WNA) for recognition of TA and CG interrupting sites, which are the intrinsic limitation for the formation of a stable triplex DNA by the natural triplex-forming oligonucleotide (TFO). However, the

Synthesis of new pyrazolo[1,5-a]pyrimidines and pyrazolo[3,4-b]pyridines

Al-Mousawi,Mohammad,Elnagdi

, p. 989 - 991 (2007/10/03)

While 3(5)-aminopyrazole reacts with enaminonitrile to yield pyrazolo[1,5-a]pyrimidines, 3-amino-5-pyrazolone reacts with the same reagents to yields pyrazolo[3,4-b]pyridines.

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