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(2R,3R)-2-Benzyloxy-nonan-3-ol is a chiral secondary alcohol with a molecular formula of C16H26O2. It features a nonan-3-ol backbone, with a benzyloxy group attached to the 2nd carbon and a hydroxyl group at the 3rd carbon. The compound is characterized by its specific stereochemistry, with the R configuration at both the 2nd and 3rd carbon atoms. This chiral center plays a crucial role in determining the compound's physical and chemical properties, as well as its potential applications in various fields, such as pharmaceuticals and organic synthesis. The presence of the benzyloxy group also imparts unique reactivity and solubility characteristics to the molecule, making it a valuable building block for the synthesis of more complex organic compounds.

81408-34-6

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81408-34-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81408-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,4,0 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81408-34:
(7*8)+(6*1)+(5*4)+(4*0)+(3*8)+(2*3)+(1*4)=116
116 % 10 = 6
So 81408-34-6 is a valid CAS Registry Number.

81408-34-6Relevant articles and documents

ZnBr2-MEDIATED HIGHLY DIASTEREOSELECTIVE ADDITION OF GRIGNARD REAGENTS TO α-BENZYLOXY ALDEHYDES

Asami, Masatoshi,Kimura, Rieko

, p. 1221 - 1222 (2007/10/02)

α-Benzyloxy aldehydes reacted with Grignard reagents in the presence of ZnBr2 to afford vicinal syn-diol derivatives with high diastereoselectivity.

Synthesis of Inhibitors of Adenosine Deaminase. A Total Synthesis of erythro-3-(Adenin-9-yl)-2-nonanol and Its Isomers from Chiral Precursors

Baker, David C.,Hawkins, L. D.

, p. 2179 - 2184 (2007/10/02)

The synthesis of both isomers of EHNA2 ("erythrohydroxynonyladenine") from D- and L-rhamnose is described.The key intermediates, (R)- and (S)-2-(benzyloxy)propanal, derived respectively from 5-O-benzyl-D- and -L-rhamnitol, were each condensed w

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