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66190-31-6

Benzenemethanol, 4-(methoxymethyl)-α-methyl-, also known as 4-(methoxymethyl)-α-methylbenzenemethanol, is an organic compound with the chemical formula C10H14O2. It is a derivative of benzyl alcohol, featuring a benzene ring with a hydroxyl group (-OH) attached to the α-carbon, which is also connected to a methyl group (-CH3). Additionally, a methoxymethyl group (-OCH2CH3) is present at the para position (4th carbon) of the benzene ring. Benzenemethanol, 4-(methoxymethyl)-a-methyl- is used as a synthetic intermediate in the production of various pharmaceuticals and agrochemicals, particularly in the synthesis of certain pesticides and drugs. Its chemical structure and functional groups make it a versatile building block in organic synthesis, allowing for further reactions and modifications to create a range of different compounds.

66190-31-6

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66190-31-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66190-31-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,1,9 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 66190-31:
(7*6)+(6*6)+(5*1)+(4*9)+(3*0)+(2*3)+(1*1)=126
126 % 10 = 6
So 66190-31-6 is a valid CAS Registry Number.

66190-31-6Downstream Products

66190-31-6Relevant articles and documents

Experimental investigations of a partial Ru-O bond during the metal-ligand bifunctional addition in noyori-type enantioselective ketone hydrogenation

Takebayashi, Satoshi,Dabral, Nupur,Miskolzie, Mark,Bergens, Steven H.

, p. 9666 - 9669 (2011)

The transition state for the metal-ligand bifunctional addition step in Noyori's enantioselective ketone hydrogenation was investigated using intramolecular trapping experiments. The bifunctional addition between the Ru dihydride trans-[Ru((R)-BINAP)(H)2((R,R)-dpen)] and the hydroxy ketone 4-HOCH2C6H4(CO)CH3 at -80 °C exclusively formed the corresponding secondary ruthenium alkoxide trans-[Ru((R)-BINAP)(H)(4-HOCH2C6H4CH(CH 3)O)((R,R)-dpen)]. Combined with the results of control experiments, this observation provides strong evidence for the formation of a partial Ru-O bond in the transition state.

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