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(2R,3R)-2-Benzyloxy-3-hydroxy-pent-4-enoic acid is a chiral organic compound characterized by its unique molecular structure. It features a pentenoic acid backbone with a 4-en-1-yl group, a hydroxyl group at the 3-position, and a benzyloxy group at the 2-position. The compound's chirality is indicated by the (2R,3R) notation, which specifies the arrangement of atoms at these positions. This molecule is of interest in the field of organic chemistry, particularly in the synthesis of complex molecules and the study of stereochemistry. Its specific structure makes it a potential candidate for various applications, such as in pharmaceuticals or as a building block for more complex organic compounds.

95832-64-7

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95832-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95832-64-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,8,3 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 95832-64:
(7*9)+(6*5)+(5*8)+(4*3)+(3*2)+(2*6)+(1*4)=167
167 % 10 = 7
So 95832-64-7 is a valid CAS Registry Number.

95832-64-7Relevant academic research and scientific papers

STEREOSPECIFIC SYNTHESIS OF Z- AND E-1-ALKOXY-1,3-BUTADIENES

Luengo, Juan I.,Koreeda, Masato

, p. 4881 - 4884 (2007/10/02)

A stereospecific, highly efficient, generally applicible synthesis of Z- and E-1-alkoxy-1,3-butadienes involving dehydrative decarboxylations of 4,5-unsaturated-2-alkoxy-3-hydroxy-carboxylic acids is described.

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