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(2R,3R)-2-Benzyloxy-4-(4-methoxy-benzyloxy)-3-methoxymethoxy-butan-1-ol is a complex organic compound characterized by its chiral center, which gives it the (2R,3R) configuration. This molecule features a butane-1-ol backbone with multiple benzyloxy and methoxymethoxy substituents. The presence of these functional groups suggests that it may have applications in the synthesis of pharmaceuticals or other specialty chemicals, where stereochemistry and functional group manipulation are crucial. The compound's structure provides a platform for further chemical reactions, potentially leading to the formation of a variety of derivatives with different properties and uses.

96016-36-3

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96016-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96016-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,0,1 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 96016-36:
(7*9)+(6*6)+(5*0)+(4*1)+(3*6)+(2*3)+(1*6)=133
133 % 10 = 3
So 96016-36-3 is a valid CAS Registry Number.

96016-36-3Downstream Products

96016-36-3Relevant academic research and scientific papers

ON THE SELECTIVITY OF DEPROTECTION OF BENZYL, MPM (4-METHOXYBENZYL)AND DMPM (3,4-DIMETHOXYBENZYL) PROTECTING GROUPS FOR HYDROXY FUNCTIONS

Horita, Kiyoshi,Yoshikoa, Tadao,Tanaka, Tatsuyoshi,Oikawa, Yuji,Yonemitsu, Osamu

, p. 3021 - 3028 (2007/10/02)

The 4-methoxybenzyl (MPM) protecting group for hydroxy functions is readily removed with DDQ in dichloromethane containing a small amount of water at room temperature.Under these neutral conditions, several other protecting and functional groups remained unchanged. 3,4-Dimethoxybenzyl (DMPM groups are more reactive than MPM groups with DDQ.The benzyl (Bn) protecting group was removed by catalitic hydrogenation over Raney nickel.Selective deprotection of DMPM, MPM and Bn groups is also presented.

DMPM (3,4-DIMETHOXYBENZYL) PROTECTING GROUP FOR HYDROXY FUNCTION MORE READILY REMOVABLE THAN MPM (P-METHOXYBENZYL) PROTECTING GROUP BY DDQ OXIDATION

Oikawa, Yuji,Tanaka, Tatsuyoshi,Horita, Kiyoshi,Yoshioka, Tadao,Yonemitsu, Osamu

, p. 5393 - 5396 (2007/10/02)

The DMPM (3,4-dimethoxybenzyl) protecting for hydroxy function was deprotected more readily than the MPM (p-methoxybenzyl) protection by DDQ oxidation under neutral conditions, and applied to the synthesis of some synthons to macrolide and polyether antib

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