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53810-61-0

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53810-61-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53810-61-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,1 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53810-61:
(7*5)+(6*3)+(5*8)+(4*1)+(3*0)+(2*6)+(1*1)=110
110 % 10 = 0
So 53810-61-0 is a valid CAS Registry Number.

53810-61-0Relevant articles and documents

HEPARANASE INHIBITORS FOR TREATMENT OF DIABETES

-

, (2021/07/10)

Anti-heparanase compounds for the treatment of diabetes are described. The anti-heparanase compounds are high affinity, synthetic glycopolymers that result in minimal anticoagulant activity. Stereoselective fluorinated forms of these compounds are also pr

HEPARANASE INHIBITORS AND THEIR USE AS ANTI-CANCER COMPOUNDS

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, (2020/07/04)

Anti-heparanase compounds for the treatment of cancer are described. The anti-heparanase compounds are high affinity, synthetic glycopolymers that result in minimal anticoagulant activity. Stereoselective fluorinated forms of these compounds are also prov

Conformational effects on glycoside reactivity: Study of the high reactive conformer of glucose

McDonnell, Ciaran,Lopez, Oscar,Murphy, Paul,Fernandez Bolanos, Jose G.,Hazell, Rita,Bols, Mikael

, p. 12374 - 12385 (2007/10/03)

The effect of conformation on glycoside reactivity was investigated by studying the hydrolysis of a selection of 3,6-anhydroglucosides as models for glucose in the highly reactive 1C4 conformation. Methyl 3,6-anhydro-β-D-glucopyranoside was found to hydrolyze 200-400 times faster than methyl glucosides in the 4C1 conformation, while methyl 3,6-anhydro-β-D-galactopyranoside, which is in the B1,4 conformation, was less reactive than methyl β-D-galactopyranoside. Methyl (3,6-anhydro-β-D-glucopyranosyl)-(1 → 6)-α-D-glucopyranoside, methyl (3,6-anhydro-α-D-glucopyranosyl)-(1 → 6)-α-D- glucopyranosyl-(1 → 6)-α-D-glucopyranoside, and methyl (3,6-anhydro-β-D-glucopyranosyl)-(1 → 6)-α-D-glucopyranosyl-(1 → 6)-α-D-glucopyranoside were prepared and found to react selectively at the anhydro residue. The finding that 1C4 conformers of glucosides are highly reactive species is in accordance with and supports previous results showing that axial OH groups are less electron withdrawing than equatorial OH groups.

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