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Cyclopentyl(triphenylmethyl) ether, also known as triphenylmethyl cyclopentyl ether, is an organic compound with the chemical formula C25H22O. It is a colorless, crystalline solid that is insoluble in water but soluble in organic solvents. This ether derivative features a cyclopentyl group attached to a triphenylmethyl (trityl) group, which is a bulky, electron-rich aryl group. The compound is used in various chemical reactions, particularly in organic synthesis, as a protecting group for alcohols due to its stability and ease of removal under mild acidic conditions. It is also employed in the synthesis of pharmaceuticals and other specialty chemicals, where its steric bulk and electronic properties can influence reaction outcomes. Cyclopentyl(triphenylmethyl) ether is a valuable tool in the chemist's toolkit for controlling reactivity and selectivity in complex molecular architectures.

1241-40-3

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1241-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1241-40-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,4 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1241-40:
(6*1)+(5*2)+(4*4)+(3*1)+(2*4)+(1*0)=43
43 % 10 = 3
So 1241-40-3 is a valid CAS Registry Number.

1241-40-3Relevant academic research and scientific papers

Indium-mediated cleavage of the trityl group from protected alcohols and diols

Behloul, Cherif,Chouti, Aicha,Guijarro, David,Foubelo, Francisco,Nájera, Carmen,Yus, Miguel

, p. 7937 - 7941 (2016/11/19)

The reaction of primary, secondary, allylic and benzylic trityl ethers with indium powder in MeOH/NH4Cl led to reductive cleavage of the trityl-oxygen bond, affording the corresponding alcohols in good to excellent yield under very mild reaction conditions. The detritylation process could successfully be extended to mono and detritylated diols. This methodology represents a new and efficient detritylation procedure under mild reaction conditions.

FeCl3-catalyzed tritylation of alcohols in ionic liquids

Sreedhar,Radhika,Neelima,Chowdary,Rao, M. V. Basaveswara

experimental part, p. 3785 - 3795 (2009/12/08)

A simple and efficient protection of alcohols as trityl ethers is described using trityl chloride in the presence of 5mol% FeCl3 as catalyst in ionic liquids at room temperature in shorter reaction times. This mild and efficient method gives access to the

Application of ball milling technology to carbohydrate reactions: I. Regioselective primary hydroxyl protection of hexosides and nucleoside by planetary ball milling

Patil, Premanand Ramrao,Kartha, K.P. Ravindranathan

, p. 279 - 293 (2008/12/21)

Dry ball milling of hexosides with trityl chloride in the presence of DABCO or Na2CO3 has been found to result in their complete conversion to the respective 6-O-trityl ethers. Further wet grinding of the reaction mixture with Ac2O in the presence of DMAP led to the respective fully protected hexosides in good to excellent yields after isolation. It has been found to be an effective one-pot two-step synthesis under solvent-free condition. The speed of homogenization has been shown to highly influence the rate and outcome of the reaction, and commercially available planetary ball mill has been proved to be very convenient for carrying out the reaction under standardized and reproducible conditions.

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