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6-Amino-1-benzyl-3-methyl-1H-pyrimidine-2,4-dione, also known as N-(1-benzyl-3-methyl-1H-pyrimidin-2-yl)acetamide, is a pyrimidine derivative with the molecular formula C14H14N4O2. It features a benzyl group attached to the nitrogen atom at position 1, endowing it with potential pharmacological properties. This chemical compound has been studied for its potential use as an antineoplastic agent and holds promise in the fields of medicinal chemistry and drug development. Its unique chemical structure also makes it a valuable intermediate in the synthesis of various organic compounds.

53681-51-9

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53681-51-9 Usage

Uses

Used in Pharmaceutical Industry:
6-Amino-1-benzyl-3-methyl-1H-pyrimidine-2,4-dione is used as an antineoplastic agent for its potential to combat cancer. Its pharmacological properties are being studied to understand its mechanism of action and efficacy in treating neoplastic diseases.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 6-Amino-1-benzyl-3-methyl-1H-pyrimidine-2,4-dione serves as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the development of new pharmaceuticals and therapeutic agents.
Used in Drug Development:
6-Amino-1-benzyl-3-methyl-1H-pyrimidine-2,4-dione is utilized in drug development for its potential to contribute to the creation of novel therapeutics. Its role as an intermediate in organic synthesis facilitates the exploration of new drug candidates and the enhancement of existing medications.

Check Digit Verification of cas no

The CAS Registry Mumber 53681-51-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,8 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53681-51:
(7*5)+(6*3)+(5*6)+(4*8)+(3*1)+(2*5)+(1*1)=129
129 % 10 = 9
So 53681-51-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H13N3O2/c1-14-11(16)7-10(13)15(12(14)17)8-9-5-3-2-4-6-9/h2-7H,8,13H2,1H3

53681-51-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-amino-1-benzyl-3-methylpyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 6-amino-1-benzyl-3-methyl uracil

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:53681-51-9 SDS

53681-51-9Relevant academic research and scientific papers

Synthesis and analytical profile of the new potent antibronchospastic agent 7-[(2,2-dimethyl)propyl]-1-methyl xanthine

Agostini,Bonacchi,Coppini,Di Marco,Paoli,Toja

, p. 684 - 688 (2007/10/02)

7-[(2,2-Dimethyl)propyl]-1-methyl xanthine (CAS 155006-67-0, MX2/120) is a new potent antibronchospastic agent with negligible side effects. The synthesis involves the alkylation of 3-benzyl-1-methyl xanthine with neopentyl bromide followed by removal of

Structure-activity relationships in a series of xanthine derivatives with antibronchoconstrictory and bronchodilatory activities

Merlos,Gomez,Vericat,Bartroli,Garcia-Rafanell,Forn

, p. 653 - 658 (2007/10/02)

Thirty-one 1,3,7,8-substituted xanthine derivatives have been synthesized and evaluated for bronchodilator and anti-bronchoconstrictory activities in in vitro tracheal relaxation and in vivo bronchospasm inhibition models. Activity tests have been complemented with phosphodiesterase inhibition and toxicological data. Structure-activity relationships are discussed. Compound 21 (1,3-diisobutyl-8-methylxanthine) has been selected for further pharmacological development because of its good activity profile and favourable therapeutic index, which is 14- and 38-fold greater than that of theophylline and IBMX, respectively.

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