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5-Hexylpyrimidine-2,4,6(1H,3H,5H)-trione is an organic compound with the molecular formula C11H16N2O3. 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 is characterized by the presence of a hexyl group (a six-carbon alkyl chain) attached to the 5-position of the pyrimidine ring. Additionally, it features three carbonyl groups (C=O) at the 2, 4, and 6 positions, which contribute to its trione classification. 5-hexylpyrimidine-2,4,6(1H,3H,5H)-trione has potential applications in various fields, including pharmaceuticals and materials science, due to its unique structure and properties.

1953-34-0

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1953-34-0 Usage

Chemical class

Pyrimidine

Molecular weight

208.25 g/mol

Main usage

Precursor in organic compound synthesis

Industries

Pharmaceutical, research, pesticide, herbicide

Special properties

Diverse chemical properties, hazardous if not handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 1953-34-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,5 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1953-34:
(6*1)+(5*9)+(4*5)+(3*3)+(2*3)+(1*4)=90
90 % 10 = 0
So 1953-34-0 is a valid CAS Registry Number.

1953-34-0SDS

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-hexyl-1,3-diazinane-2,4,6-trione

1.2 Other means of identification

Product number -
Other names 5-hexyl-barbituric acid

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:1953-34-0 SDS

1953-34-0Downstream Products

1953-34-0Relevant academic research and scientific papers

Reduction of Isopropylidene Acylmalonates, 5-Acylbarbituric Acids, and 3-Acyl-4-hydroxycoumarins to the Corresponding Alkyl Derivatives by Sodium Cyanoborohydride-Acetic Acid

Nutaitis, Charles F.,Schultz, Rose Ann,Obaza, Judy,Smith, Francis X.

, p. 4606 - 4608 (2007/10/02)

Isopropylidene acylmalonates, 5-acylbarbituric acids, and 3-acyl-4-hydroxycoumarins are readily reduced to the corresponding alkyl derivatives by sodium cyanoborohydride-acetic acid.The cyclic substrates are readily prepared by the acylation of isopropylidene malonate, barbituric acid (or its N,N'-dimethyl derivative), and 4-hydroxycoumarin, according to procedures developed by other workers.The reductions take place upon addition of a 2 mol equiv of sodium cyanoborohydride to a mixture of the acyl compound and acetic acid.This reductive transformation completes a synthetic method for the preparation of the alkyl derivatives starting from the parent compound.

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