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((2R,3S)-2-Isopropyl-4-oxo-3-phenyl-oxetan-3-yl)-acetic acid methyl ester is a complex organic compound with the molecular formula C16H18O4. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific 2R,3S configuration. ((2R,3S)-2-Isopropyl-4-oxo-3-phenyl-oxetan-3-yl)-acetic acid methyl ester features an isopropyl group, a phenyl ring, and an oxetan ring, which contributes to its unique structure and properties. It is an ester derivative of a 4-oxo-3-phenyloxetan-3-yl acetic acid, with a methyl group attached to the carboxylic acid moiety. This chemical is typically synthesized for use in pharmaceutical research and development, particularly in the synthesis of complex molecules and as a potential intermediate in the production of certain drugs. Its specific applications and properties are determined by its structural features, which can influence its reactivity and interaction with other molecules.

92979-31-2

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92979-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92979-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,7 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92979-31:
(7*9)+(6*2)+(5*9)+(4*7)+(3*9)+(2*3)+(1*1)=182
182 % 10 = 2
So 92979-31-2 is a valid CAS Registry Number.

92979-31-2Relevant academic research and scientific papers

STEREOSELECTIVE ADDITIONS TO CARBOXYLIC ACID DIANIONS AND β-LACTONE SUBSTITUTED ESTER ENOLATES. APPLICATION TO THE SYNTHESIS OF RACEMIC EPI-BLASTMYCINONE, δ-MULTISTRIATINE, PARACONIC ESTERS AND LIGNANTYPE DILACTONES

Mulzer, Johann,Lasalle, Peter de,Chucholowski, Alexander,Blaschek, Ursula,Bruentrup, Gisela,et al.

, p. 2211 - 2218 (2007/10/02)

New stereoselective syntheses are reported for racemic 4-epi-blastmycinone (6) and δ-multistriatine (13) utilizing the anti-configurated γ,δ-unsaturated β-hydroxy-carboxylic acids 2a/b.A diastereo- and enantioselective aldoltype addition of phenylacetic acid dianion to benzaldehyde has been achaived by employing optically active alkoxide amide bases.Finally, highly stereocontrolled additions to the novel β-lactone substituted ester enolates 22 are described.

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