87581-70-2 Usage
Derivative of pyrazole
Contains a pyrazole ring as the main structural component
Contains a hydroxyl group
A polar functional group (-OH) attached to the pyrazole ring
Contains a methyl group
A small alkyl group (-CH3) attached to the pyrazole ring
Commonly used in pharmaceutical and organic synthesis
Utilized as a building block or intermediate in the synthesis of various pharmaceutical and organic compounds
Exhibits potential biological activities
Shows possible interactions with biological systems, potentially leading to therapeutic effects or other biological functions
Highly reactive
The presence of the hydroxyl and methyl groups makes the compound reactive, allowing it to participate in various chemical reactions
Aromatic substitution on the pyrazole ring
The presence of an aromatic group (4-methylphenyl) attached to the pyrazole ring contributes to the compound's properties and potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 87581-70-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,8 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87581-70:
(7*8)+(6*7)+(5*5)+(4*8)+(3*1)+(2*7)+(1*0)=172
172 % 10 = 2
So 87581-70-2 is a valid CAS Registry Number.
87581-70-2Relevant academic research and scientific papers
Arylpyrazolylcarbinol compounds with analgesic activity
-
, (2008/06/13)
The present invention relates to novel arylheteroarylcarbinol derivatives with analgesic activity and to their therapeutically acceptable salts. These novel derivatives correspond to the general formula I: STR1 in which: R1, R2 and R
ALPHA-LITHIATION OF N-ALKYL GROUPS IN PYRAZOLES
Katritzky, Alan R.,Jayaram, Chandra,Vassilatos, Socrates N.
, p. 2023 - 2029 (2007/10/02)
1,3,5-Trimethylpyrazole and 1-ethyl-3,5-dimethylpyrazole undergo lithiation exclusively at the α-position of the N-alkyl group. 1-Benzylpyrazole is metallated under kinetic control at -78 deg C at the CH2 group, but the metallorganic intermediate rearrang
