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(2R,3R)-2-Benzyl-butane-1,3-diol is a chiral organic compound with the molecular formula C11H16O2. It is a secondary alcohol, featuring a benzyl group attached to a butane-1,3-diol backbone. The compound exhibits two chiral centers at the 2nd and 3rd carbon atoms, resulting in four possible stereoisomers. The specific (2R,3R) configuration indicates that both chiral centers have the R configuration, meaning that the hydroxyl groups are positioned on the right side when traversing the molecule from the lowest to the highest priority substituent. (2R,3R)-2-Benzyl-butane-1,3-diol is of interest in the field of organic chemistry, particularly in the synthesis of complex molecules and pharmaceuticals, due to its unique stereochemistry and potential for functional group manipulation.

90107-06-5

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90107-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90107-06-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,0 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90107-06:
(7*9)+(6*0)+(5*1)+(4*0)+(3*7)+(2*0)+(1*6)=95
95 % 10 = 5
So 90107-06-5 is a valid CAS Registry Number.

90107-06-5Downstream Products

90107-06-5Relevant academic research and scientific papers

Silylmethyl Radical Cyclization: New Stereoselective Method for 1,3-Diol Synthesis from Allylic Alcohols

Nishiyama, Hisao,Kitajima, Toshio,Matsumoto, Makoto,Itoh, Kenji

, p. 2298 - 2300 (2007/10/02)

Cyclizations of (bromomethyl)dimethylsilyl allylic ethers by treatment with tri-n-butyltin hydride in a free-radical process followed by oxidation in a one-pot manner with hydrogen peroxide gave th corresponding 1,3-diols predominantly with high stereoselectivity.

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