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1-benzyl-3-phenyldihydropyrimidine-2,4(1H,3H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21575-64-4

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21575-64-4 Usage

Chemical structure

A dihydropyrimidine-2,4(1H,3H)-dione derivative with a benzyl group at the 1-position and a phenyl group at the 3-position.

Potential pharmaceutical applications

The compound has been studied for its potential medical uses, such as its role as an anti-inflammatory and anxiolytic agent.

Neuropharmacology

1-benzyl-3-phenyldihydropyrimidine-2,4(1H,3H)-dione has shown promise in the field of neuropharmacology, particularly in the treatment of neurodegenerative diseases and psychiatric disorders.

Antitumor properties

The compound has been investigated for its potential antitumor properties, which could lead to the development of new therapeutic agents for cancer treatment.

Antiviral properties

Research on 1-benzyl-3-phenyldihydropyrimidine-2,4(1H,3H)-dione has also explored its potential as an antiviral agent, which could be useful in the development of new treatments for viral infections.

Further research

Additional studies on 1-benzyl-3-phenyldihydropyrimidine-2,4(1H,3H)-dione and its derivatives may lead to the development of new therapeutic agents with a wide range of clinical applications.

Molecular weight

The molecular weight of 1-benzyl-3-phenyldihydropyrimidine-2,4(1H,3H)-dione is approximately 295.32 g/mol.

Solubility

The solubility of the compound in various solvents may vary, but it is generally more soluble in organic solvents like ethanol, methanol, and dimethyl sulfoxide (DMSO) than in water.

Stability

The stability of 1-benzyl-3-phenyldihydropyrimidine-2,4(1H,3H)-dione may depend on factors such as temperature, light exposure, and the presence of other chemicals or substances. Proper storage conditions should be maintained to ensure the compound's stability for research and potential pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 21575-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,5,7 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 21575-64:
(7*2)+(6*1)+(5*5)+(4*7)+(3*5)+(2*6)+(1*4)=104
104 % 10 = 4
So 21575-64-4 is a valid CAS Registry Number.

21575-64-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-3-phenyl-1,3-diazinane-2,4-dione

1.2 Other means of identification

Product number -
Other names 1-benzyl-3-phenyl-dihydro-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:21575-64-4 SDS

21575-64-4Downstream Products

21575-64-4Relevant academic research and scientific papers

A convenient preparation of 1,3-disubstituted dihydro-2,4-(1H,3H) pyrimidinediones

Deck,Papadopoulos

, p. 675 - 680 (2007/10/03)

The ureas 3 which are obtained from 3-(benzylamino)propanenitrile (1) and various isocyanates (2) cyclize readily upon heating in ethanol, in the presence of hydrochloric acid, to form 3-substituted 1-benzyldihydro-2,4-(1H,3H)pyrimidinediones (11) in good

Solid-phase synthesis of 5,6-dihydropyrimidine-2,4-diones

Kolodziej, Stephen A.,Hamper, Bruce C.

, p. 5277 - 5280 (2007/10/03)

A series of 1,3-disubstituted-5,6-dihydropyrimidine-2,4-diones 1 are prepared by solid phase organic chemistry using a cyclization-cleavage strategy from readily available amines and isocyanates. A acrylate ester of Wangs resin is treated with primary amines to afford N-substituted β-aminoesters followed by treatment with isocyanates to afford β-ureido ester 4. Cyclization-cleavage of the bound ureido ester under acidic conditions gave direct formation of 5,6-dihydropyrimidinedione 1.

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