906477-25-6 Usage
General Description
2-(2-Fluorophenyl)-1H-imidazol-5-yl]methanol is a chemical compound with the molecular formula C10H9FN2O. It is a white to off-white crystalline powder and is used as a building block for the synthesis of various pharmaceutical compounds. This chemical is typically used in the pharmaceutical industry for the development of drugs targeting specific biological pathways. It may also be used as a reagent in organic synthesis and as a reference standard in analytical chemistry. 2-(2-FLUOROPHENYL)-1H-IMIDAZOL-5-YL]METHANOL is important in the field of medicinal chemistry for the development of new drugs and therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 906477-25-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,4,7 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 906477-25:
(8*9)+(7*0)+(6*6)+(5*4)+(4*7)+(3*7)+(2*2)+(1*5)=186
186 % 10 = 6
So 906477-25-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H9FN2O/c11-9-4-2-1-3-8(9)10-12-5-7(6-14)13-10/h1-5,14H,6H2,(H,12,13)
906477-25-6Relevant articles and documents
PYRROLOPYRIMIDINES AS CFTR POTENTIATORS
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Paragraph 0503; 0504, (2018/06/04)
The present invention relates to compounds of Formula I, wherein R1a, R1b, R2, R3, R4, W, Y, and Z are as described herein, and pharmaceutically acceptable salts thereof. The compounds are potentiator
2-Phenyl-4-(aminomethyl)imidazoles as Potential Antipsychotic Agents. Synthesis and Dopamine D2 Receptor Binding
Thurkauf, Andrew,Hutchison, Alan,Peterson, John,Cornfield, Linda,Meade, Robin,et al.
, p. 2251 - 2255 (2007/10/02)
A series of 2-phenyl-4-(aminomethyl)imidazoles were designed as conformationally restricted analogs of the dopamine D2 selective benzamide antipsychotics.The title compounds were synthesized and tested for blockade of YM-09151 binding in cloned African green monkey dopamine D2 receptor preparations.The binding affinity data thus obtained were compared against that of the benzamides and a previously described series of 2-phenyl-5-(aminomethyl)pyrroles.
