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5-(Benzyloxymethyl)uracil is a chemical compound derived from uracil, a nucleobase present in RNA, with a benzyl group attached to the oxygen atom. This modification is believed to enhance the compound's antiviral activity by improving its stability and cellular uptake, making it a promising candidate for the treatment of viral infections.

7295-02-5

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7295-02-5 Usage

Uses

Used in Pharmaceutical Industry:
5-(Benzyloxymethyl)uracil is used as a potential antiviral agent for the treatment of viral infections. Its unique structure allows for increased stability and cellular uptake, which may contribute to its effectiveness in inhibiting the replication of certain viruses.
Used in Research and Development:
5-(Benzyloxymethyl)uracil is utilized in laboratory studies to explore its antiviral properties and to investigate its potential as a therapeutic agent for various viral infections. This research is crucial for understanding the compound's mechanisms of action and for developing new strategies to combat viral diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 7295-02-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,9 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7295-02:
(6*7)+(5*2)+(4*9)+(3*5)+(2*0)+(1*2)=105
105 % 10 = 5
So 7295-02-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2O3/c15-11-10(6-13-12(16)14-11)8-17-7-9-4-2-1-3-5-9/h1-6H,7-8H2,(H2,13,14,15,16)

7295-02-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(BENZYLOXYMETHYL)URACIL

1.2 Other means of identification

Product number -
Other names Propanimidamide,2-hydroxy-2-methyl

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:7295-02-5 SDS

7295-02-5Relevant academic research and scientific papers

Pyrimidine 2,4-Diones in the design of new HIV RT inhibitors

Romeo, Roberto,Iannazzo, Daniela,Veltri, Lucia,Gabriele, Bartolo,Macchi, Beatrice,Frezza, Caterina,Marino-Merlo, Francesca,Giofrè, Salvatore V.

, (2019/05/27)

The pyrimidine nucleus is a versatile core in the development of antiretroviral agents. Onthis basis, a series of pyrimidine-2,4-diones linked to an isoxazolidine nucleus have been synthesized and tested as nucleoside analogs, endowed with potential anti-

Sulfonamide derivatives

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Page column 145, (2010/02/05)

A compound of the formula (I) or a pharmacologically acceptable salt, ester or other derivative thereof: R1is H or NHOH. R2is H, optionally substituted alkyl, cycloalkyl or a group —AR6. A is an alkylene which may be optionally interrupted by O, —S(O)m— or —N(R9). R6is a group (II), (III), (IV) X is O, S, —N(R10)—, —C(R11)(R12)—. Y is O, CO, —S(O)n—, —N(R10)—, —C(R11)(R12)—. Each of R7and R8is H, alkyl, COOH, optionally substituted alkyl, etc. Each of R9, R10, R11, and R12is H, alkyl, etc. Each of m and n is 0 to 2. R3is H, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl, optionally substituted alkynyl. R4is optionally substituted (hetero)arylene. R5is optionally substituted alkyl, optionally substituted (hetero)aryl. These compounds have matrixmetalloproteinase—13 inhibitory activity and aglycanase inhibitory activity.

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