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The chemical "1-[O3,O5-bis-(4-methyl-benzoyl)-α-D-erythro-2-deoxy-pentofuranosyl]-1H-pyrimidine-2,4-dione" is a complex organic molecule with a unique structure. It features a pyrimidine-2,4-dione core, which is a common structural motif in various biologically active compounds. The molecule is further characterized by the presence of a 2-deoxy-pentofuranosyl sugar moiety, which is crucial for its interaction with biological targets. The sugar is modified with two 4-methyl-benzoyl groups at the O3 and O5 positions, which may contribute to the molecule's stability and reactivity. This specific arrangement of functional groups suggests that the compound could have potential applications in medicinal chemistry, possibly as a precursor to antiviral or anticancer drugs, given the structural similarities to known nucleoside analogs.

4449-37-0

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4449-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4449-37-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,4 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4449-37:
(6*4)+(5*4)+(4*4)+(3*9)+(2*3)+(1*7)=100
100 % 10 = 0
So 4449-37-0 is a valid CAS Registry Number.

4449-37-0Downstream Products

4449-37-0Relevant academic research and scientific papers

Investigation of Stereoselectivities in the Coupling Reactions of 1-O-Methyl-3,5-di-O-p-toluoyl-2-deoxyribofuranoside with Purines and Pyrimidines

Janardhanam, Selvasekaran,Nambiar, Krishnan P.

, p. 3657 - 3660 (2007/10/02)

Stereoselectivities in the coupling rection between 1-O-methyl-3,5-di-O-p-toluoyl-2-deoxyribofuranoside and suitably protected purine and pyrimidine derivatives have been examined in acetonitrile with varying equivalents of SnCl4.The best result in α-nucleoside formation was obtained when the coupling reaction was carried out in the presence of ten equivalents of SnCl4.

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