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5-Ethylsulfanylmethyluracil, also known as 5-ethoxy-2-[(methylsulfanyl)methyl]pyrimidin-4(3H)-one, is a chemical compound belonging to the family of uracil derivatives. It is recognized for its antiviral properties and potential applications in both antiviral and cancer therapy.

4874-41-3

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4874-41-3 Usage

Uses

Used in Antiviral Applications:
5-Ethylsulfanylmethyluracil is used as an antiviral agent for its potential activity against a variety of viruses, including herpes simplex virus type 1 and 2, varicella-zoster virus, and human cytomegalovirus. It functions by inhibiting viral DNA polymerase, which interferes with viral replication, thereby helping to control and prevent the spread of these viral infections.
Used in Cancer Therapy:
5-Ethylsulfanylmethyluracil is also being investigated for its potential use in cancer therapy due to its antiproliferative properties. It has shown promise in preclinical and clinical trials, suggesting that it may be a valuable addition to the arsenal of cancer treatment options, particularly for those seeking novel therapeutic approaches.

Check Digit Verification of cas no

The CAS Registry Mumber 4874-41-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4874-41:
(6*4)+(5*8)+(4*7)+(3*4)+(2*4)+(1*1)=113
113 % 10 = 3
So 4874-41-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2O2S/c1-2-12-4-5-3-8-7(11)9-6(5)10/h3H,2,4H2,1H3,(H2,8,9,10,11)

4874-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(ethylsulfanylmethyl)-1H-pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-Ethyl-thiomethyl-uracil

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:4874-41-3 SDS

4874-41-3Downstream Products

4874-41-3Relevant academic research and scientific papers

5-Ethylthiomethyl- and 5-Ethylsulfonylmethylpyrimidines

Eichberger, Guenter,Hayden, Walter,Schwarz, Wolfgang,Griengl, Herfried

, p. 385 - 392 (2007/10/02)

In 2,4-dichloro-5-ethylthiomethylpyrimidines 3a,b and in (2,4-dichloro-5-pyrimidinylmethyl)ethyl sulfones 5a,b, resp., by reaction with ammonia, diethylamine, isopropylamine, sodium methanolate and sodium ethylthiolate, resp., the halogen atoms have been substituted by amino, methoxy or ethylthio groups, resp., and thus the compounds 4a-4r and 5c-5f have been obtained.Keywords: Halogen exchange, in pyrimidines; Pyrimidines, 5-ethylsulfonyl-methyl-; Pyrimidines, 5-ethylthiomethyl-

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