36039-35-7 Usage
Uses
Used in Pharmaceutical Industry:
4-(2-Methylpropyl)benzeneethanol is used as a key intermediate in the synthesis of carboxylate-related compounds with potential anti-inflammatory activity. Its role in the pharmaceutical industry is crucial for the development of new anti-inflammatory drugs.
Used in Synthesis of Ibuprofen:
4-(2-Methylpropyl)benzeneethanol is used as a starting material in the synthesis of ibuprofen, a widely used nonsteroidal anti-inflammatory drug (NSAID), via carbonylation. This process highlights its importance in the production of pain-relieving and anti-inflammatory medications.
Check Digit Verification of cas no
The CAS Registry Mumber 36039-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,3 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 36039-35:
(7*3)+(6*6)+(5*0)+(4*3)+(3*9)+(2*3)+(1*5)=107
107 % 10 = 7
So 36039-35-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O/c1-10(2)9-12-5-3-11(4-6-12)7-8-13/h3-6,10,13H,7-9H2,1-2H3
36039-35-7Relevant academic research and scientific papers
Reductive cleavage of acetals and ketals with 9-borabicyclo[3.3.1]nonane
Soderquist, John A.,Kock, Iveliz,Estrella, Maria E.
, p. 1076 - 1079 (2012/12/23)
The reductive cleavage of benzaldehyde acetals and acetophenone ketals with the air-stable crystalline 9-borabicyclo[3.3.1]-nonane dimer provides monobenzylated ether derivatives of diols and 1,2-oxygen-transposed β-phenethyl alcohols, respectively. The boron moiety is effectively recovered through simple procedures which involve convenient air-stable reagents and boron byproducts. The process is particularly selective for 1,3-diols giving the more substituted monobenzyl ether derivatives exclusively. With acetophenone ketals both reduction and elimination occur, permitting 9-BBN-H to hydroborate the resulting styrene to produce 1,2-oxygen-transposed β-phenethyl alcohols cleanly. Potential applications of this new process were illustrated with the synthesis of the hallucinogen, mescaline, and the analgesic, ibufenac.
