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(2R,3R)-1,4-bis(benzyloxy)-3-methyl-2-butanol is a chiral organic compound characterized by its unique molecular structure. It features a 2-butanol backbone with a methyl group at the 3-position and two benzyloxy groups at the 1 and 4 positions. The compound is a liquid at room temperature and is soluble in common organic solvents. Due to its chiral nature, it exists as a pair of enantiomers, with the (2R,3R) configuration being one of the two possible forms. (2R,3R)-1,4-bis(benzyloxy)-3-methyl-2-butanol is often used as an intermediate in the synthesis of more complex organic molecules, particularly in the pharmaceutical and chemical industries, where its stereochemistry plays a crucial role in determining the properties and reactivity of the final product.

84906-48-9

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84906-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84906-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,0 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 84906-48:
(7*8)+(6*4)+(5*9)+(4*0)+(3*6)+(2*4)+(1*8)=159
159 % 10 = 9
So 84906-48-9 is a valid CAS Registry Number.

84906-48-9Relevant academic research and scientific papers

Synthetic studies on fully substituted γ-pyrone-containing natural products: The absolute configurations of Ilikonapyrone and peroniatriols I and II

Arimoto, Hirokazu,Cheng, Ji-Fei,Nishiyama, Shigeru,Yamamura, Shosuke

, p. 5781 - 5784 (2007/10/02)

Mild cyclization method [DMSO - (COCl)2 or Ph3P - CCl4] of triketides bearing optically active functional groups to the corresponding γ-pyrones provided determination of the absolute configurations of ilikonapyrone and per

Method for the total synthesis of cyclosporins, novel cyclosporins and novel intermediates and methods for their production

-

, (2008/06/13)

A method for the total synthesis of cyclosporins, in particular Cyclosporin A, cyclosporins produced in accordance with the method of the invention and novel intermediates, in particular novel [1S, 2R, 3R]- and [1R, 2S, 3S]-1-nitrilo-1-carbonyl-3-methyl-2-oxy-heptanes and -hept-5-enes, employed in the method of the invention.

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