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(1R,2S)-2-Benzyloxymethyl-cyclopropanol is a chiral organic compound with a cyclopropane ring, featuring a benzyloxy group attached to the 2-carbon and a hydroxyl group at the 1-carbon. (1R,2S)-2-Benzyloxymethyl-cyclopropanol is characterized by its unique three-membered carbon ring structure, which imparts significant ring strain and makes it a valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals. The specific stereochemistry at the 1- and 2-positions (1R,2S) is crucial for its reactivity and potential applications, as it can influence the compound's biological activity and selectivity in chemical reactions.

96503-88-7

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96503-88-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96503-88-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,5,0 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 96503-88:
(7*9)+(6*6)+(5*5)+(4*0)+(3*3)+(2*8)+(1*8)=157
157 % 10 = 7
So 96503-88-7 is a valid CAS Registry Number.

96503-88-7Downstream Products

96503-88-7Relevant academic research and scientific papers

Applications of Cyclopropylboranes in Organic Synthesis. 1. A Stereocontrolled Route to Substituted Cyclopropanol Derivatives

Danheiser, Rick L.,Savoca, Ann C.

, p. 2401 - 2403 (1985)

Secondary and tertiary cyclopropanols are produced stereoselectively via the sequential treatment of 1,1-dibromocyclopropanes with n-butyllithium, catecholborane (or trialkylborane) and alkaline hydrogen peroxide.

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