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(2R,3R)-2,4-Bis-benzyloxy-3-methyl-butan-1-ol is a complex organic compound with the molecular formula C19H24O3. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific 2R,3R configuration. (2R,3R)-2,4-Bis-benzyloxy-3-methyl-butan-1-ol features a butan-1-ol backbone with a methyl group at the 3rd carbon, and two benzyloxy groups attached to the 2nd and 4th carbons. The benzyloxy groups are derived from benzyl alcohol, which is a phenylmethyl group attached to a hydroxyl group. (2R,3R)-2,4-Bis-benzyloxy-3-methyl-butan-1-ol is often used in organic synthesis, particularly in the preparation of more complex molecules, due to its ability to serve as a protecting group for hydroxyl functions. It is also notable for its potential applications in the pharmaceutical industry, where it may be used as an intermediate in the synthesis of drugs. The compound's structure and properties make it a valuable tool in the hands of chemists, allowing for the creation of a wide range of molecules with diverse applications.

92979-25-4

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92979-25-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92979-25-4 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, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92979-25:
(7*9)+(6*2)+(5*9)+(4*7)+(3*9)+(2*2)+(1*5)=184
184 % 10 = 4
So 92979-25-4 is a valid CAS Registry Number.

92979-25-4Downstream Products

92979-25-4Relevant 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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