63121-26-6 Usage
Uses
Used in Pharmaceutical Industry:
(1S-trans)-hexahydro-1H-Pyrrolizin-1-ol is used as a key building block in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, (1S-trans)-hexahydro-1H-Pyrrolizin-1-ol serves as an essential component in the creation of novel agrochemicals. Its incorporation can lead to the development of more effective and targeted pest control solutions.
Used in Fine Chemicals Production:
(1S-trans)-hexahydro-1H-Pyrrolizin-1-ol is utilized as a fundamental building block in the production of fine chemicals. Its versatility in organic synthesis contributes to the creation of specialty chemicals for various applications.
Used in Organic Synthesis Research:
Due to its unique structure and properties, (1S-trans)-hexahydro-1H-Pyrrolizin-1-ol is also used in research for organic synthesis. It aids chemists in exploring new synthetic pathways and developing innovative chemical compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 63121-26-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,2 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63121-26:
(7*6)+(6*3)+(5*1)+(4*2)+(3*1)+(2*2)+(1*6)=86
86 % 10 = 6
So 63121-26-6 is a valid CAS Registry Number.
63121-26-6Relevant academic research and scientific papers
Pyrrolizidines VI: Stereoselective Synthesis of 1- and 2-(8S)-Pyrrolizidinones and Investigation of their Reductions with Complex Boron Hydrides
Gundermann, Harald,Schnekenburger, Joerg
, p. 925 - 929 (2007/10/02)
Starting with (S)-proline the title compounds are stereoselectively synthesized and subsequently reduced by complex boron hydrides.These reductions are studied with regard to their stereochemistry and possible mechanism.During the reduction of 1-(8S)-pyrrolizidinone (3) with lithium borohydride 1-(8S)-pyrrolizidinone borane 3a is isolated, this compound is assumed to be a reaction intermediate.
