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(3R)-hexa-3,4-dien-1-yl 4-nitrobenzoate is a chemical compound with the molecular formula C13H13NO4. It is a chiral molecule, meaning it has a non-superimposable mirror image, and the R configuration at the 3rd carbon indicates the specific arrangement of atoms in the molecule. (3R)-hexa-3,4-dien-1-yl 4-nitrobenzoate features a hexa-3,4-dien-1-yl group, which is a conjugated diene with a double bond at the 3rd and 4th carbons, and a 4-nitrobenzoate group, which is a benzoic acid derivative with a nitro group at the 4th position. The conjugated diene system and the nitro group contribute to the compound's reactivity and properties, making it potentially useful in organic synthesis and as a building block for more complex molecules.

5689-24-7

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5689-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5689-24-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,8 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5689-24:
(6*5)+(5*6)+(4*8)+(3*9)+(2*2)+(1*4)=127
127 % 10 = 7
So 5689-24-7 is a valid CAS Registry Number.

5689-24-7Downstream Products

5689-24-7Relevant academic research and scientific papers

Enantioselective synthesis of 5,7-bicyclic ring systems from axially chiral allenes using a Rh(I)-catalyzed cyclocarbonylation reaction

Grillet, Francois,Brummond, Kay M.

, p. 3737 - 3754 (2013/06/04)

A transfer of chirality in an intramolecular Rh(I)-catalyzed allenic Pauson-Khand reaction (APKR) to access tetrahydroazulenones, tetrahydrocyclopenta[c]azepinones and dihydrocyclopenta[c]oxepinones enantioselectively (22-99% ee) is described. The substit

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