107862-65-7 Usage
Description
5,6-Dihydro-4H-pyrrolo[1,2-b]pyrazole is a heterocyclic compound belonging to the pyrazole family. It is characterized by its unique chemical structure, which features a fused pyrrolo ring with a pyrazole ring. 5,6-Dihydro-4H-pyrrolo[1,2-b]pyrazole is known for its potential applications in various fields, particularly in the pharmaceutical and chemical industries, due to its versatile chemical properties.
Uses
Used in Pharmaceutical Industry:
5,6-Dihydro-4H-pyrrolo[1,2-b]pyrazole is used as a key intermediate in the synthesis of withasomnine molecules, which are pyrazole alkaloids. These alkaloids are known for their anti-inflammatory and analgesic properties, making them valuable in the development of new drugs for the treatment of pain and inflammation.
Used in Chemical Industry:
In the chemical industry, 5,6-Dihydro-4H-pyrrolo[1,2-b]pyrazole can be utilized as a building block for the creation of various complex molecules and compounds. Its unique structure allows for further functionalization and modification, enabling the development of new materials with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 107862-65-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,8,6 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 107862-65:
(8*1)+(7*0)+(6*7)+(5*8)+(4*6)+(3*2)+(2*6)+(1*5)=137
137 % 10 = 7
So 107862-65-7 is a valid CAS Registry Number.
107862-65-7Relevant articles and documents
New synthetic route to the alkaloid withasomnine by ring transformation of a functionalized cyclopropanol via the parent pyrrolo[1,2-b]pyrazole
Kulinkovich, Oleg,Masalov, Nikolai,Tyvorskii, Vladimir,De Kimpe, Norbert,Keppens, Marian
, p. 1095 - 1096 (2007/10/03)
Withasomnine has been prepared by rearrangement of 1-(3-chloropropyl)-cyclopropanol into 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole, followed by bromination and [NiCl2(dppp)]-catalyzed phenylation.
