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5-Butylpyrimidine-2,4(1H,3H)-dione is a chemical compound with the molecular formula C9H12N2O2. It is a derivative of pyrimidine, a heterocyclic aromatic organic compound consisting of a six-membered ring containing four carbon atoms and two nitrogen atoms. The compound features a butyl group (a four-carbon alkyl chain) attached to the 5th position of the pyrimidine ring and two carbonyl groups (C=O) at the 2nd and 4th positions. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its role as an intermediate in the production of other organic compounds. Due to its unique structure, 5-butylpyrimidine-2,4(1H,3H)-dione can participate in various chemical reactions, such as nucleophilic substitution, addition, and condensation, making it a versatile building block in organic synthesis.

5442-52-4

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5442-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5442-52-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5442-52:
(6*5)+(5*4)+(4*4)+(3*2)+(2*5)+(1*2)=84
84 % 10 = 4
So 5442-52-4 is a valid CAS Registry Number.

5442-52-4SDS

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-butyl-1H-pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-Butyluracil

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:5442-52-4 SDS

5442-52-4Relevant academic research and scientific papers

Nucleosides. 136. Synthesis and antiviral effects of several 1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-5-alkyluracils. Some structure-activity relationships

Su,Watanabe,Schinazi,Fox

, p. 151 - 154 (2007/10/02)

In order to study structure-activity relationships between antiherpetic activity and the size of the C-5 alkyl substituents of 2'-fluoro-ara-U derivatives, six new nucleosides (1c-h) were synthesized. The 5-allyl analogue 1c was prepared by a Pd(II)-catal

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