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Methyl 3'-O-benzoyl-2,3-O-isopropylidene-β-D-apiofuranoside is a complex organic compound with the molecular formula C16H20O6. It is a derivative of β-D-apiofuranoside, a naturally occurring sugar found in various plants. The compound features a methyl group attached to the anomeric carbon, a benzoyl group at the 3' position, and an isopropylidene protecting group at the 2,3 positions. This chemical structure is significant in the field of carbohydrate chemistry, as it represents a protected form of the sugar, which can be used in the synthesis of more complex molecules or as a precursor in organic synthesis. The compound's properties, such as its solubility and reactivity, are influenced by these functional groups, making it a valuable intermediate in the preparation of pharmaceuticals and other bioactive compounds.

5517-60-2

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  • ((3aR,4R,6R,6aR)-6-Methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl benzoate

    Cas No: 5517-60-2

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5517-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5517-60-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,1 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5517-60:
(6*5)+(5*5)+(4*1)+(3*7)+(2*6)+(1*0)=92
92 % 10 = 2
So 5517-60-2 is a valid CAS Registry Number.

5517-60-2Relevant articles and documents

Conversion of: N- acyl amidines to amidoximes: A convenient synthetic approach to molnupiravir (EIDD-2801) from ribose

Ahmed, Ajaz,Ahmed, Qazi Naveed,Mukherjee, Debaraj

, p. 36143 - 36147 (2021/12/04)

An efficient method is described for the preparation of molnupiravir (EIDD-2801) an antiviral agent via regioselective conversion of an N-acyl-nucleoside intermediate, generated through stereo and regioselective glycosylation of protected ribose and N4-acetyl cytosine, to an amidoxime. This method avoids use of expensive starting materials, enzymes, complex reagents, and cumbersome purification procedures.

Synthesis and biological evaluation of novel apio nucleosides with thiazole-4-carboxamide and 1,2,4-triazole-3-carboxamide

Kim, Myong Jung,Jeong, Lak Shin,Kim, Joong Hyup,Shin, Ji Hye,Chung, Soon Yong,Lee, Sang Kook,Chun, Moon Woo

, p. 715 - 724 (2007/10/03)

In view of biological activities of azole nucleosides and apio-dideoxynucleoside, novel apio nucleoside analogues (1 and 2) with thiazole and triazole base moiety were synthesized using 2,3-O-isopropylidene-apio-β -D-furanose (3), which was prepared from D-mannose.

A Simple Synthesis of α-D-Ribofuranosides

Bock, Klaus,Refn, Susanne

, p. 324 - 327 (2007/10/02)

The glycosylation of various aglycones with 5-O-benzoyl-2,3-O-isopropylidene-β-D-ribofuranosyl bromide (2) has been studied under different reaction conditions.It is possible to obtain high yields of α-linked ribofuranosides using methanol or methyl-2,3-O

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