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Methyl 4,6-di-O-benzoyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside is a complex organic compound with the molecular formula C20H18O6. It is a derivative of a hexopyranoside, which is a type of sugar molecule. The compound features a methyl group attached to the 4th and 6th carbon atoms, which are both substituted with benzoyl groups. The 2nd and 3rd carbon atoms are dideoxy, meaning they lack two oxygen atoms, and the molecule has a double bond between the 2nd and 3rd carbon atoms. methyl 4,6-di-O-benzoyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside is often used in organic synthesis and as a building block for more complex molecules, particularly in the field of carbohydrate chemistry. Its structure and properties make it a valuable intermediate in the synthesis of various biologically active compounds and pharmaceuticals.

6605-37-4

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6605-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6605-37-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,0 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6605-37:
(6*6)+(5*6)+(4*0)+(3*5)+(2*3)+(1*7)=94
94 % 10 = 4
So 6605-37-4 is a valid CAS Registry Number.

6605-37-4Relevant academic research and scientific papers

Effective and chemoselective glycosylations using 2,3-unsaturated sugars

Kusumi, Shunichi,Sasaki, Kaname,Wang, Sainan,Watanabe, Tatsuya,Takahashi, Daisuke,Toshima, Kazunobu

experimental part, p. 3164 - 3178 (2010/08/21)

Glycosyl donors containing a double bond between C2 and C3 were designed by mimicking the reaction mechanism of lysozyme-initiated hydrolysis of mucopolysaccharides. It was found that, under various glycosylation conditions, the reactivities of 2,3-unsatu

An efficient glycosidation method using 2,3-unsaturated glycosyl donors

Sasaki, Kaname,Matsumura, Shuichi,Toshima, Kazunobu

, p. 9039 - 9043 (2007/10/03)

A novel class of 'armed' glycosyl donors containing a double bond at the C-2 position was designed by mimicking the mechanism of lysozyme-initiated hydrolysis. These donors were used to achieve chemoselective glycosidation of hex-2-enopyranosyl acetate an

TRANSACETALISATION PROCESS

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Page/Page column 50, (2010/02/13)

The invention relates to the resolution of racemic mixtures, and in particular to the separation of enantiomers of chiral alcohols utilising recyclable chiral auxiliaries. The present invention also relates to a process for preparing these recyclable chiral auxiliaries using an enantiomerically pure alcohol.

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