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(1R,2S)-2-Benzyloxymethoxy-3-methyl-1-phenyl-butan-1-ol is a complex organic compound with the molecular formula C20H24O3. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific stereochemistry, with the R configuration at the first carbon and the S configuration at the second carbon. (1R,2S)-2-Benzyloxymethoxy-3-methyl-1-phenyl-butan-1-ol features a benzyloxymethoxy group attached to the second carbon, a methyl group at the third carbon, and a phenyl group at the first carbon. It is a secondary alcohol, with the hydroxyl group attached to the first carbon. This specific arrangement of functional groups and stereochemistry gives the compound unique chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research.

83876-96-4

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83876-96-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83876-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,7 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83876-96:
(7*8)+(6*3)+(5*8)+(4*7)+(3*6)+(2*9)+(1*6)=184
184 % 10 = 4
So 83876-96-4 is a valid CAS Registry Number.

83876-96-4Downstream Products

83876-96-4Relevant academic research and scientific papers

Stereochemical Consequences of Carbanion Asymmetry. An Access to 1,2-Diols

McGarvey, Glenn J.,Kimura, Masayuki

, p. 5420 - 5422 (2007/10/02)

The enantiofacial discrimination of some asymmetric α-alkoxy carbanions is described, as well as an illustration of their preparative utility.

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