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Methyl 3-acetamido-4,6-di-O-acetyl-2,3-dideoxy-α-D-lyxo-hexopyranoside is a complex organic compound with the molecular formula C14H21NO8. It is a derivative of a sugar molecule, specifically a hexopyranoside, which is a six-carbon sugar ring. The compound features an acetamido group at the 3-position, which is an amide derived from acetic acid. Additionally, it has two acetyl groups at the 4 and 6 positions, which are ester groups derived from acetic acid. The molecule is also characterized by the absence of two hydroxyl groups (dideoxy) at the 2 and 3 positions, which is a modification of the parent sugar structure. methyl 3-acetamido-4,6-di-O-acetyl-2,3-dideoxy-α-D-lyxo-hexopyranoside is a potential intermediate in the synthesis of various biologically active molecules and may be used in the preparation of complex carbohydrates and related pharmaceuticals. Its α-D-lyxo configuration refers to the specific arrangement of hydroxyl groups on the sugar ring, which is important for its chemical properties and potential applications.

3369-63-9

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3369-63-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3369-63-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,6 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3369-63:
(6*3)+(5*3)+(4*6)+(3*9)+(2*6)+(1*3)=99
99 % 10 = 9
So 3369-63-9 is a valid CAS Registry Number.

3369-63-9Upstream product

3369-63-9Downstream Products

3369-63-9Relevant academic research and scientific papers

The use of tri-O-acetyl-D-glucal and -D-galactal in the synthesis of 3-acetamido-2,3-dideoxyhexopyranoses and -hexopyranosides.

Liberek, Beata,Dabrowska, Aleksandra,Frankowski, Ryszard,Matuszewska, Marlena,Smiatacz, Zygfryd

, p. 1803 - 1810 (2002)

Addition of hydrazoic acid to alpha,beta-unsaturated aldehydes derived from tri-O-acetyl-D-glucal and -D-galactal gave 3-azido-2,3-dideoxyhexopyranoses. These were converted into 1,4,6-tri-O-acetyl-3-azido-2,3-dideoxyhexopyranoses as well as methyl and ethyl glycosides. Hydrogenation of the proamine group in 3-azido-2,3-dideoxy derivatives provided different 3-amino and 3-acetamido sugars. The configuration and conformation of all products were established on the basis of the 1H and 13 C NMR, IR and polarimetric data.

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