2655-35-8 Usage
Chemical class
Pyrazole derivative
Pyrazole ring
A five-membered ring with two nitrogen atoms
3,5-dimethyl substitution
Two methyl groups attached to the pyrazole ring at the 3rd and 5th positions
Phenylethane group
A phenyl group connected to an ethyl group
Organic synthesis
Used as a building block in the synthesis of more complex organic molecules
Pharmaceutical research
Investigated for potential biological activities and drug development
Enzyme inhibition
Acts as an inhibitor for certain enzymes
Receptor modulation
Interacts with specific receptors, potentially affecting their function
Coordination chemistry
Used as a ligand, forming complexes with metal ions
Drug development
May contribute to the creation of new pharmaceuticals
Material development
Could be used in the synthesis of novel materials with specific properties
Check Digit Verification of cas no
The CAS Registry Mumber 2655-35-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,5 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2655-35:
(6*2)+(5*6)+(4*5)+(3*5)+(2*3)+(1*5)=88
88 % 10 = 8
So 2655-35-8 is a valid CAS Registry Number.
2655-35-8Relevant academic research and scientific papers
Iridium-Catalyzed Regio- and Enantioselective Borylation of Unbiased Methylene C(sp3)?H Bonds at the Position β to a Nitrogen Center
Du, Rongrong,Liu, Luhua,Xu, Senmiao
supporting information, p. 5843 - 5847 (2021/02/01)
Reported herein is the pyrazole-directed iridium-catalyzed enantioselective borylation of unbiased methylene C?H bonds at the position β to a nitrogen center. The combination of a chiral bidentate boryl ligand, iridium precursor, and pyrazole directing group was responsible for the high regio- and enantioselectivity observed. The method tolerated a vast array of functional groups to afford the corresponding C(sp3)?H functionalization products with good to excellent enantioselectivity.
1-Chloromethyl-3,5-dimethylpyrazole hydrochloride. A useful synthetic intermediate
Katritzky, Alan R.,Lam, Jamshed N.
, p. 1144 - 1147 (2007/10/02)
1-Chloromethyl-3,5-dimethylpyrazole hydrochloride readily undergoes nucleophilic displacement with O-, N-, or S-nucleophiles. 1-Phenylthiomethyl-3,5-dimethylpyrazole can be lithiated at the CH2 group and reacted with alkyl halides and carbonyl
