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5-Acetyluracil, also known as 1,3-dihydro-1,3-dioxo-5-s-triazin-2(1H)-one, is a chemical compound derived from uracil, a nucleobase present in RNA and DNA. It is primarily used as an intermediate in the synthesis of antiviral and anticancer drugs, showcasing its potential in inhibiting the replication of certain viruses and contributing to the development of novel pharmaceuticals.

6214-65-9

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6214-65-9 Usage

Uses

Used in Pharmaceutical Industry:
5-Acetyluracil is used as an intermediate in the synthesis of antiviral and anticancer drugs for its potential antiviral properties and its role in creating novel pharmaceuticals.
Used in Antiviral Applications:
5-Acetyluracil is used as an antiviral agent for its ability to inhibit the replication of certain viruses, making it a valuable component in the development of antiviral medications.
Used in Anticancer Drug Development:
5-Acetyluracil is used as a building block in the synthesis of various anticancer drugs, contributing to the creation of innovative and effective cancer treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 6214-65-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,1 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6214-65:
(6*6)+(5*2)+(4*1)+(3*4)+(2*6)+(1*5)=79
79 % 10 = 9
So 6214-65-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O3/c1-3(9)4-2-7-6(11)8-5(4)10/h2H,1H3,(H2,7,8,10,11)

6214-65-9 Well-known Company Product Price

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  • TCI America

  • (A2670)  5-Acetyluracil  >98.0%(HPLC)(T)

  • 6214-65-9

  • 1g

  • 660.00CNY

  • Detail
  • TCI America

  • (A2670)  5-Acetyluracil  >98.0%(HPLC)(T)

  • 6214-65-9

  • 5g

  • 2,750.00CNY

  • Detail
  • Alfa Aesar

  • (44378)  5-Acetyluracil, 98%   

  • 6214-65-9

  • 1g

  • 680.0CNY

  • Detail
  • Alfa Aesar

  • (44378)  5-Acetyluracil, 98%   

  • 6214-65-9

  • 5g

  • 2825.0CNY

  • Detail
  • Alfa Aesar

  • (44378)  5-Acetyluracil, 98%   

  • 6214-65-9

  • 25g

  • 12377.0CNY

  • Detail
  • Aldrich

  • (570648)  5-Acetyluracil  97%

  • 6214-65-9

  • 570648-1G

  • 664.56CNY

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6214-65-9SDS

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 5-acetyl-1H-pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-acetyl-2,6-dioxo-1,3-dihydropyrimidine

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:6214-65-9 SDS

6214-65-9Relevant academic research and scientific papers

Investigation on possibility of rearrangement of pyrimidine-5-carboxylic acids esters

Scherbinina,Dar'In,Lobanov

experimental part, p. 1109 - 1115 (2011/10/02)

A previously reported rearrangement of pyrimidine-5-carboxylic acids esters to 5-acylpyrimidones does not, in fact, occur in any of the examples studied by us.

HIV integrase inhibitors with nucleobase scaffolds: Discovery of a highly potent anti-HIV agent

Nair, Vasu,Chi, Guochen,Ptak, Roger,Neamati, Nouri

, p. 445 - 447 (2007/10/03)

HIV integrase is essential for HIV replication. However, there are currently no integrase inhibitors in clinical use for AIDS. We have discovered a conceptually new β-diketo acid that is a powerful inhibitor of both the 3′-processing and strand transfer s

Isomerization/recyclization of some 5-ethoxycarbonyl-pyrimidines

Vardanyan,Hruby,Danagulyan,Mkrtchyan

, p. 557 - 562 (2007/10/03)

This communication reports on the investigation of a new recyclization conversion of a pyrimidine ring, which can be referred to as C-C recyclization. In this reaction the nucleophile cleaves the pyrimidine ring at the N(3)-C(4) bond, and following rotation around the single C(5)-C(6) bond the new cyclization takes place. This type of recyclization has general applicability, and takes place upon alkali treatment of substituted 4-methyl-5-ethoxycarbonyl- and 4-amino-5-ethoxycarbonyl-pyrimidines (1) which are transformed respectively to 4-hydroxy-5-acetyl- and 4-hydroxy-5-carbamoylpyrimidines (2). The obtained pyrimidyl-ketones can be readily converted to their hydrazones 7-12.

CYCLIZATION DICHOTOMY OF ESTERS OF 3-UREIDO-2-CYANO-2-PROPENOIC AND 3-UREIDO-2-ACYL-2-PROPENOIC ACIDS

Ledvina, Miroslav,Farkas, Jiri

, p. 1841 - 1852 (2007/10/02)

The preparation of E and Z isomers of 3-ureido-2-cyano-2-propenoates Ia-Id and their base-catalyzed isomerization and cyclization to 5-carboxycytosine derivatives IIa-IIf and 5-cyanouracil derivatives IIIa and IIIb is described.Also described is the preparation of 3-ureido-2-acyl-2-propenoates Va-Vd and their base-catalyzed cyclization to 5-carboxy-2(1H)-pyrimidone derivatives VIa-VIc and 5-acyluracils VIIa-VIIc.

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