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(1R,2S)- and (1S,2R)-1-hydroxy-2-(dibenzylamino)cyclobutane-1-acetic acid, t-butyl ester are two enantiomeric forms of a complex organic compound. These molecules are characterized by their chiral centers, which result in different spatial arrangements of the atoms around the chiral carbons. The (1R,2S)-enantiomer has a hydroxyl group on the first carbon and a dibenzylamino group on the second carbon, while the (1S,2R)-enantiomer has the opposite configuration. Both compounds are esters, with a t-butyl group attached to the carboxylic acid moiety, which can influence their reactivity and stability. These compounds are of interest in organic chemistry and may have potential applications in pharmaceuticals or as chiral building blocks in the synthesis of more complex molecules.

89519-19-7

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89519-19-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89519-19-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,1 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89519-19:
(7*8)+(6*9)+(5*5)+(4*1)+(3*9)+(2*1)+(1*9)=177
177 % 10 = 7
So 89519-19-7 is a valid CAS Registry Number.

89519-19-7Relevant academic research and scientific papers

Stereospecific Synthesis of (1S,2S)-1-Hydroxy-2--cyclobutane-1-acetic Acid, a Novel Microbial Antimetabolite

Adlington, Robert M.,Baldwin, Jack E.,Jones, Richard H.,Murphy John A.,Parisi, Melchiorre F.

, p. 1479 - 1481 (2007/10/02)

The unusual-cyclobutane containing dipeptide (1S,2S)-1-hydroxy-2-cyclobutane-1-acetic acid (1), produced by an as yet unidentified Streptomyces species X-1092 was synthesised via a short stereospecific route.

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