132407-66-0 Usage
Uses
Used in Pharmaceutical Applications:
[1-(2-Fluorophenyl)-1H-pyrrol-2-yl]methanol is used as a building block in the organic synthesis and medicinal chemistry for the development of new drugs and biologically active compounds. Its structural features and potential biological activity make it a promising candidate for further research and development in the pharmaceutical industry.
Used in Organic Synthesis:
In the field of organic synthesis, [1-(2-Fluorophenyl)-1H-pyrrol-2-yl]methanol serves as a valuable intermediate for the creation of more complex molecules. Its unique structure allows for various chemical reactions and modifications, which can lead to the synthesis of novel compounds with specific properties and applications.
Further research and studies are necessary to fully understand the properties and potential uses of [1-(2-Fluorophenyl)-1H-pyrrol-2-yl]methanol, as its current applications are based on its structural features and potential biological activity.
Check Digit Verification of cas no
The CAS Registry Mumber 132407-66-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,4,0 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132407-66:
(8*1)+(7*3)+(6*2)+(5*4)+(4*0)+(3*7)+(2*6)+(1*6)=100
100 % 10 = 0
So 132407-66-0 is a valid CAS Registry Number.
132407-66-0Relevant articles and documents
A convenient synthesis of pyrrolo[2,1-c][1,4] benzoxazines
Sanchez, Isabel,Pujol, Maria Dolors
, p. 5593 - 5598 (2007/10/03)
The pyrrolo[2,1-c][1,4]benzoxazine system was synthesized from 2- fluoroaniline involving an intramolecular nucleophilic displacement of the fluoride atom. The intermediate alcohols 7a and 10 were treated in basic media under strictly controlled condition
Polycondensed Heterocycles. VI. A New Efficient Synthesis of 4H-Pyrrolobenzothiazines
Nacci, V.,Campiani, G.,Garofalo, A.
, p. 3019 - 3029 (2007/10/02)
A novel and efficient method to obtain 4H-pyrrolo benzothiazine and its 4-alkyl and 4-aryl derivatives via an intramolecular nucleophilic aromatic fluoride displacement has been developed.
