66120-51-2 Usage
General Description
1-(6-methylpyridin-2-yl)propan-2-ol, also known as 6-methyl-2-pyridinylisobutanol, is a chemical compound with the molecular formula C10H13NO. It is a tertiary alcohol that is commonly used in the pharmaceutical industry as a chiral building block for the synthesis of various drugs and bioactive compounds. Due to its unique structure, it exhibits different properties and reactivity compared to other alcohols, making it valuable for medicinal chemistry and drug discovery research. 1-(6-methylpyridin-2-yl)propan-2-ol is also used as a reagent in organic synthesis and is known for its mild and selective oxidation capabilities. Additionally, it has been reported to have potential anti-inflammatory and anti-cancer activities, further adding to its significance in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 66120-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,1,2 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 66120-51:
(7*6)+(6*6)+(5*1)+(4*2)+(3*0)+(2*5)+(1*1)=102
102 % 10 = 2
So 66120-51-2 is a valid CAS Registry Number.
66120-51-2Relevant articles and documents
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Quick et al.
, p. 2705 (1978)
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Efficient Water Reduction with sp3-sp3 Diboron(4) Compounds: Application to Hydrogenations, H–D Exchange Reactions, and Carbonyl Reductions
Flinker, Mathias,Yin, Hongfei,Juhl, René W.,Eikeland, Espen Z.,Overgaard, Jacob,Nielsen, Dennis U.,Skrydstrup, Troels
supporting information, p. 15910 - 15915 (2017/11/23)
A series of crystalline sp3-sp3 diboron(4) compounds were synthesized and shown to promote the facile reduction of water with dihydrogen formation. The application of these diborons as simple and effective dihydrogen and dideuterium sources was demonstrated by conducting a series of selective reductions of alkynes and alkenes, and hydrogen–deuterium exchange reactions using two-chamber reactors. Finally, as the water reduction reaction generates an intermediate borohydride species, a range of aldehydes and ketones were reduced by using water as the hydride source.
