138836-03-0 Usage
Uses
Used in Pharmaceutical Industry:
Cyclopropanol, 2,2-dimethyl-1-pyrazinylis used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique structure allows it to be a key component in the development of new medications, potentially leading to innovative treatments for a range of diseases.
Used in Agrochemical Industry:
In the agrochemical field, Cyclopropanol, 2,2-dimethyl-1-pyrazinylis used as a building block for the creation of novel pesticides and herbicides. Its potential biological activity makes it a valuable asset in the development of more effective and environmentally friendly agricultural chemicals.
Further Research:
Due to the compound's unique structure and potential applications, further research is needed to fully understand its properties and potential uses. This includes exploring its biological activity, stability, and how it can be synthesized and incorporated into various products for maximum efficacy and safety.
Check Digit Verification of cas no
The CAS Registry Mumber 138836-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,8,3 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 138836-03:
(8*1)+(7*3)+(6*8)+(5*8)+(4*3)+(3*6)+(2*0)+(1*3)=150
150 % 10 = 0
So 138836-03-0 is a valid CAS Registry Number.
138836-03-0Relevant articles and documents
Triplet states mediating hydrogen abstraction in 4-acylpyrimidines, 2-acylpyridines, 2-acylpyrazines, and 3-acylpyridazines
Prathapan, Sreedharan,Robinson, Kevin E.,Agosta, William C.
, p. 1838 - 1843 (1992)
Irradiation of 9 leads to hydrogen abstraction by N(1) and fragmentation to 8 from a triplet with ET ～78 kcal/mol. Irradiation of 2-acylpyridines (10) leads to abstraction by both nitrogen and oxygen (cf. eq 4), with the same Stern-Volmer kqτ for the two processes. Irradiation of 2-acylpyrazines (11) can lead to abstraction by either nitrogen (φ27 0.77 from 11b) or oxygen (φ11a 0.95 from 11f)- 3-Acylpyridazine 12d is unreactive on direct irradiation or triplet sensitization with sensitizer ET ～70 kcal/mol; it furnishes a small amount of 12a on sensitization by acetone. Ketone 18 is recovered unchanged from irradiation under all conditions used with 12d. These observations suggest a correlation between the photochemistry of each of these compounds and the energy of the nπ* triplet of the heteroaromatic ring. The nature of the excited state(s) responsible for hydrogen abstraction by nitrogen and oxygen in these ketones is discussed.
