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28485-24-7

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28485-24-7 Usage

Chemical structure

A pyrimidine derivative with two benzyl groups attached to the 1st and 5th positions, and a carbonyl group at the 2nd and 4th positions.

Appearance

Typically a solid or crystalline compound.

Biological activities

Exhibits antiviral and anticancer properties.

Organic synthesis

Used as a building block in the synthesis of various pharmacologically active compounds.

Pharmaceutical research

Investigated for its potential therapeutic applications in medicinal and pharmaceutical fields.

Solubility

Soluble in organic solvents such as methanol, ethanol, and dimethyl sulfoxide (DMSO).

Stability

Generally stable under normal laboratory conditions, but sensitive to heat, light, and moisture.

Purity

Often synthesized with a high degree of purity for use in research and pharmaceutical applications.

Safety precautions

Handle with care, as it may have potential toxic effects. Use appropriate personal protective equipment (PPE) and follow proper disposal procedures.

Storage

Store in a cool, dry, and dark place, preferably in airtight containers to protect from light and moisture.

Check Digit Verification of cas no

The CAS Registry Mumber 28485-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,4,8 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28485-24:
(7*2)+(6*8)+(5*4)+(4*8)+(3*5)+(2*2)+(1*4)=137
137 % 10 = 7
So 28485-24-7 is a valid CAS Registry Number.

28485-24-7SDS

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 1,5-dibenzylpyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 1,5-dibenzyl-1H-pyrimidine-2,4-dione

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:28485-24-7 SDS

28485-24-7Downstream Products

28485-24-7Relevant articles and documents

Sodium hydride mediated cascade reaction towards the synthesis of 1,5-disubstituted uracil from cyanamides derived from Baylis-Hillman adducts

Nag,Yadav,Maulik,Batra

, p. 911 - 917 (2007/12/27)

The substituted cyanamides generated from Baylis-Hillman adducts afford 1,5-disubstituted uracils via a sodium hydride induced cascade reaction involving sequential intramolecular attack of the hydroxy group on the nitrile group, cyclization of the result

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