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2,4(1H,3H)-Pyrimidinedione, 5-methyl-1-[[2-(phenylmethoxy)-1-[(phenylmethoxy)methyl]ethoxy]methyl] - is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90056-89-6

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90056-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90056-89-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,5 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90056-89:
(7*9)+(6*0)+(5*0)+(4*5)+(3*6)+(2*8)+(1*9)=126
126 % 10 = 6
So 90056-89-6 is a valid CAS Registry Number.

90056-89-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-<<2-(benzyloxy)-1-<(benzyloxy)methyl>ethoxy>methyl>thymine

1.2 Other means of identification

Product number -
Other names 1-[(1,3-dibenzyloxy-2-propoxy)methyl]-5-methyluracil

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:90056-89-6 SDS

90056-89-6Downstream Products

90056-89-6Relevant academic research and scientific papers

PREVENTION AND TREATMENT OF CANCER AND OTHER DISEASES

-

Page/Page column 64, (2008/06/13)

Nucleoside chemical compounds, which interact with specific structures of deoxyribonucleic acid (DNA) or ribonucleic acid (RNA) are disclosed. The compounds interfere with the activities of telomerase and reverse transcriptase, and are useful as antivirals, antibacterials and anticancer agents. Methods of treating or preventing cancers in patients involving administration of a therapeutically effective amount of a composition having an inhibitor or antagonist of the reverse transcriptases (RTs) expressed in cells of the patients are also disclosed. Method of using nucleoside analogs and other inhibitors of RTs in conjunction with DNA damaging agents such as genotoxic agents or radiation or photodynamic therapy or combinations these for the treatment of various cancers are also disclosed.

Effect of Acyclic Pyrimidines Related to 9-guanine on Herpesviruses

Beauchamp, Lilia M.,Serling, Barbara L.,Kelsey, John E.,Biron, Karen K.,Collins, Peter,et al.

, p. 144 - 149 (2007/10/02)

A series of pyrimidines related to the potent antiherpetic agent 9-guanine (1, BW B759U), all containing the same acyclic chain, have been synthesized.Some of the compounds were derivatives of the naturally occuring bases, cytosine, uracil, and thymine; others included compounds in which the 5-position of the cytosine and uracil moieties were substituted by bromo, iodo, fluoro, methyl, and amino groups.Other variations of the cytosine derivatives were the 5-aza, 2-mercapto, 4-methylamino, 4-dimethylamino, and isocytosine congeners.A 4-aminopyrimidine adduct was also made.Antiviral testing showed that 1-cytosine (18, BW A1117U) was equivalent to the guanine analogue in the potency against human cytomegalovirus and Epstein Barr virus.Other compounds in the series were largely inactive in antiviral screening against the herpesviruses.

Uracil analogues of the acylonucleoside 9--methyl>guanine (BIOLF-62)

Ogilvie, Kelvin K.,Hamilton, Raymond G.,Gillen, Michael F.,Radatus, Bruno K.,Smith, Kendall O.,Galloway, Karen S.

, p. 16 - 21 (2007/10/02)

A series of substituted uracil analogues of the antiviral agent 9-methyl>guanine (BIOL-62) has been synthesized and characterized.The uracil analogues show little activity against herpesviruses.

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