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(3R,5S)-3-Bromo-5-phenyl-tetrahydro-furan-2-ol is a chiral organic compound characterized by its unique molecular structure. It features a tetrahydrofuran ring, which is a saturated analog of furan, with a hydroxyl group at the 2-position. The compound is further distinguished by the presence of a bromine atom at the 3-position and a phenyl group at the 5-position. The stereochemistry is specified as (3R,5S,) indicating the specific arrangement of these substituents in three-dimensional space. (3R,5S)-3-Bromo-5-phenyl-tetrahydro-furan-2-ol is of interest in organic chemistry and may have applications in the synthesis of pharmaceuticals or other specialty chemicals due to its unique structural features and potential reactivity.

99344-36-2

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99344-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99344-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,4 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 99344-36:
(7*9)+(6*9)+(5*3)+(4*4)+(3*4)+(2*3)+(1*6)=172
172 % 10 = 2
So 99344-36-2 is a valid CAS Registry Number.

99344-36-2Upstream product

99344-36-2Downstream Products

99344-36-2Relevant academic research and scientific papers

Etude d'α-bromo-butyrolactones; application a la preparation du methyl-3 phenyl-4 Δ2 butenolide et du methyl-2 phenyl-1 butene-2 diol-1,4 de configuration Z

Gharbi-Benarous, Josyane,Morales-Rios, Martha S.,Dana, Gilbert

, p. 2384 - 2389 (2007/10/02)

Starting from 2,3-dihydrofuranic compounds, we prepare the corresponding α-bromohydrines and α-bromo-butyrolactones.A solvolytic method of equilibration of these bromolactones in DMF is described.All the stereoisomers are separated and studied.With a Cβ s

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