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1-(4-dimethylaminophenyl)-2-methylpropan-1-ol, also known as 4-(dimethylamino)phenyl-2-methylpropan-1-ol, is an organic compound with the molecular formula C12H19NO. It is a derivative of 2-methylpropan-1-ol (tert-butanol) with a 4-dimethylaminophenyl group attached to the carbon atom. 1-(4-dimethylaminophenyl)-2-methylpropan-1-ol is characterized by its amine group, which gives it basic properties, and its phenyl ring, which contributes to its aromatic nature. It is a colorless to pale yellow liquid and is used in the synthesis of various pharmaceuticals and chemical intermediates. Due to its amine group, it can form salts with acids and is known for its reactivity in organic synthesis. The compound is also recognized for its potential applications in the development of dyes and pigments, as well as in the production of certain types of polymers.

4278-81-3

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4278-81-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4278-81-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,7 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4278-81:
(6*4)+(5*2)+(4*7)+(3*8)+(2*8)+(1*1)=103
103 % 10 = 3
So 4278-81-3 is a valid CAS Registry Number.

4278-81-3Relevant academic research and scientific papers

A Reinvestigation of the Meerwein-Ponndorf-Verley Reduction: A Highly Efficient Variation Using Zirconium Catalysts

Knauer, Birgit,Krohn, Karsten

, p. 677 - 684 (2007/10/02)

A new variation of the Meerwein-Ponndorf-Verley reduction based on mechanistic considerations is presented.Under optimized conditions 1-(4-dimethylaminophenyl)ethanol was used as the reducing alcohol (2-4 equiv.), Zr(O-tBu)4 as the catalyst (0.2 equiv.), and toluene or cyclohexane as the solvent.Aldehydes and ketones (if not extremely sterically hindered) were reduced to the corresponding alcohols at room temperature mostly within 2-4 h in essentially quantitative yield. α,β-Unsaturated carbonyl compounds cleanly react in a 1,2-mode to afford the corresponding allylic alcohols. - Key Words: Reductions / Meerwein-Ponndorf-Verley reaction / Catalysis / Zirconium tetra-tert-butoxide / β-Hydride shift / Kinetics

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