60907-90-6 Usage
Description
Benzenemethanol, -alpha-,2,3-trimethyl(9CI) is an organic compound with the molecular formula C9H12O. It is a derivative of benzyl alcohol, featuring two methyl groups at the 2nd and 3rd positions on the benzene ring. Benzenemethanol, -alpha-,2,3-trimethyl(9CI) is known for its unique chemical properties and potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
Benzenemethanol, -alpha-,2,3-trimethyl(9CI) is used as a reagent for the synthesis of α-adrenoreceptor agonists, which are essential in veterinary medicine. These agonists exhibit analgesic and sedative activities, making them valuable for managing pain and calming animals during medical procedures.
Used in Chemical Synthesis:
Benzenemethanol, -alpha-,2,3-trimethyl(9CI) is also utilized as an intermediate in the production of Dexmedetomidine (D299000), an α2-Adrenergic agonist. Benzenemethanol, -alpha-,2,3-trimethyl(9CI) serves as an impurity in the synthesis process, which is crucial for ensuring the purity and quality of the final product. Benzenemethanol, -alpha-,2,3-trimethyl(9CI)'s unique structure allows for further chemical modifications and the development of new pharmaceutical agents with potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 60907-90-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,9,0 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 60907-90:
(7*6)+(6*0)+(5*9)+(4*0)+(3*7)+(2*9)+(1*0)=126
126 % 10 = 6
So 60907-90-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O/c1-7-5-4-6-10(8(7)2)9(3)11/h4-6,9,11H,1-3H3
60907-90-6Relevant articles and documents
Synthesis and enantiomeric resolution of medetomidine
Fakhraian,Toulabi,Choobdari,Peyrovi,Ghanbary, H. Hadj
, p. 141 - 148 (2015/05/20)
Medetomidine {4-[l-(2,3-dimethylphenyl)ethyl]-3H-imidazole], 5} is a selective α2-adrenoceptor agonist used in veterinary medicine for its analgesic and sedative properties. It is also an alternative and environmentally acceptable anti-fouling biocide which impedes the settlement of barnacles at nanomolar concentrations and replaces toxic antifouling coatings based on heavy metals. Several syntheses of medetomidine have been reported. The first method for the preparation of 5 and of other related 4-benzylimidazoles was described in a patent starting from 2,3-dimethylbromobenzene as shown in Scheme 1; unfortunately the yields were not reported.
PROCESS FOR THE PREPARATION OF MEDETOMIDINE
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Page/Page column 15-16, (2009/05/28)
A process of preparing Medetomidine of Formula (I) or an acid addition salt thereof, which process comprises: (i) reacting 2,3-dimethyl-methylbenzylalcohol with N-trimethylsilylimidazole, and, if desired, converting the Medetomidine to an acid addition salt thereof.