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6160-55-0

Methyl 3,5-di-O-benzyl-2-deoxy-β-D-erythro-pentofuranoside is a complex organic compound with the molecular formula C18H22O5. It is a derivative of a pentose sugar, specifically a 2-deoxy-pentose, which is a type of sugar that lacks an oxygen atom on the second carbon. The compound features a methyl group attached to the first carbon, and benzyl groups (a phenylmethyl group) are attached to the third and fifth carbons. This chemical structure is significant in organic chemistry and biochemistry, as it represents a protected form of a sugar that can be used in the synthesis of more complex molecules, such as nucleosides and other biologically active compounds. The benzyl groups serve as protecting groups, which can be removed under specific conditions to reveal the underlying sugar structure. methyl 3,5-di-O-benzyl-2-deoxy-β-D-erythro-pentofuranoside is often used in the synthesis of pharmaceuticals and other biologically relevant molecules due to its stability and the ease with which it can be modified.

6160-55-0

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6160-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6160-55-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,6 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6160-55:
(6*6)+(5*1)+(4*6)+(3*0)+(2*5)+(1*5)=80
80 % 10 = 0
So 6160-55-0 is a valid CAS Registry Number.

6160-55-0Relevant articles and documents

Synthesis and Antiviral Activity of Acyclic Nucleosides with a 3(S),5-Dihydroxypentyl of 4(R)-Methoxy-3(S),5-dihydroxypentyl Side Chain

Vandendriessche, Frank,Snoeck, Robert,Janssen, Gerard,Hoogmartens, Jos,Aerschot, Arthur Van,et al.

, p. 1458 - 1465 (2007/10/02)

Optically pure acyclic nucleoside analogues with a 3(S),5-dihydroxypentyl or 4(R)-methoxy-3(S),5-dihydroxypentyl side chain were synthesized starting from 2-deoxy-D-ribose.The acyclic nucleosides were obtained by alkylation of the bases with the mesylates

A NEW SYNTHETIC METHOD FOR γ-BUTYROLACTOLS BY THE PALLADIUM-CATALYZED REGIOSELECTIVE OXIDATION OF 1-ALKEN-4-OLS

Nokami, Junzo,Ogawa, Hideki,Miyamoto, Shinya,Mandai, Tadakatsu,Wakabayahi, Shoji,Tsuji, Jiro

, p. 5181 - 5184 (2007/10/02)

3-substituted 1-alken-4-ols were oxidized with PdCl2-benzoquinone regioselectively at the terminal carbon to afford cyclic hemiacetals (γ-butyroacetols), which were converted to γ-butiroacetones by the Jones oxidation.This reactions was applied to the synthesis of optically active deoxyribose and γ-butenolides.

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