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8-(benzyloxy)-9-pentofuranosyl-3,9-dihydro-1H-purine-2,6-dione is a complex organic compound with the molecular formula C18H19N5O5. It is a derivative of the purine family, which includes important biological molecules such as adenine and guanine. This specific compound features a benzyloxy group attached to the 8-position of the purine ring, a pentofuranosyl sugar moiety at the 9-position, and a dihydro structure. The compound is characterized by its 1H-purine-2,6-dione structure, indicating the presence of two carbonyl groups at the 2 and 6 positions of the purine ring. This chemical is of interest in the field of medicinal chemistry and may have potential applications in the development of new therapeutic agents, particularly in the area of antiviral drugs, due to its structural similarity to nucleoside analogs.

3868-37-9

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3868-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3868-37-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,6 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3868-37:
(6*3)+(5*8)+(4*6)+(3*8)+(2*3)+(1*7)=119
119 % 10 = 9
So 3868-37-9 is a valid CAS Registry Number.

3868-37-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-8-phenylmethoxy-3H-purine-2,6-dione

1.2 Other means of identification

Product number -
Other names 8-benzyloxy-xanthosine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3868-37-9 SDS

3868-37-9Relevant academic research and scientific papers

Oxidation of 9-β-d-ribofuranosyl uric acid by one-electron oxidants versus singlet oxygen and its implications for the oxidation of 8-oxo-7,8-dihydroguanosine

Nguyen, Khiem V.,Muller, James G.,Burrows, Cynthia J.

, p. 2176 - 2180 (2011/05/05)

Uric acid, a cellular antioxidant, undergoes oxidation in the presence of one-electron oxidants as well as singlet oxygen. In the present work, the oxidation pathways and products formed from oxidation of the uric acid nucleoside are compared to the more commonly studied uric acid free base. A wider distribution of products, including allantoin, urea, caffolide, and 5-carboxamido-5-hydroxyhydantoin nucleosides, are formed when the N9 position of uric acid is glycosylated. The oxidation pathways share some features in common with the oxidation of 8-oxo-7,8-dihydroguanosine, but the additional spectrum of products implies that the combination of oxidative and deaminative damage to guanosine may lead to a more complex set of DNA lesions than originally described.

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