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ethyl N-acetyl-5-amino-3,4,5-trideoxy-4-ethyl-6,7:8,9-di-O-isopropylidene-D-glycero-D-talo-non-2-ulofuranosonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1024599-38-9

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1024599-38-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1024599-38-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,4,5,9 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1024599-38:
(9*1)+(8*0)+(7*2)+(6*4)+(5*5)+(4*9)+(3*9)+(2*3)+(1*8)=149
149 % 10 = 9
So 1024599-38-9 is a valid CAS Registry Number.

1024599-38-9Downstream Products

1024599-38-9Relevant academic research and scientific papers

An unexpected elimination product leads to 4-alkyl-4-deoxy-4-epi-sialic acid derivatives

Hemeon, Ivan,Bennet, Andrew J.

, p. 238 - 247 (2008)

A useful, unexpected β,γ-unsaturated-α-keto ester (ethyl (E)-5-acetamido-3,4,5-trideoxy-6,7:8,9-di-O-isopropylidene-D-manno-non-3-en-2- ulosonate 5) was isolated in 91% yield following ozonolysis and chromatographic purification of its enoate ester precursor ethyl 5-acetamido-2,3,4,5-tetradeoxy- 6,7:8,9-di-O-isopropylidene-2-methylene-4-nitro-D-glycero-D-galacto-nononate (6). When the 4R enoate ester (ethyl 5-acetamido-2,3,4,5-tetradeoxy-6,7:8,9-di- O-isopropylidene-2-methylene-4-nitro-D-glycero-D-talo-nononate, 7) was subjected to the same conditions, enone 5 was a minor product (18%) while the major product did not eliminate HNO2 but instead cyclized to form a five-membered ring containing a hemiaminal linkage between C-2 and the amide nitrogen on C-5 (9, 70%). Conjugate addition, to enone 5 opens up the potential to generate 4-substituted sialic acid derivatives, a general route to such compounds that has not been previously reported. In a preliminary investigation of such a route, diethylzinc and dimethylzinc were added to enone 5 resulting in generation of 4-alkyl-substituted cyclic hemiaminal structures 11 and 13, which could be deprotected to form 2,7-anhydrosialic acid analogues 14 and 15. These products could then be converted to peracetylated glycals 16 and 17, the 4-methyl-substituted compound 17 being finally deprotected to give a 4-methyl-substituted analogue of the glycal of sialic acid (5-acetamido-2,6- anhydro-3,4,5-trideoxy-4-methyl-D-glycero-D-talo-non-2-enonic acid 18).

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