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2-amino-6-methyl-1,5-dihydropyrimido[5,4-d]pyrimidine-4,8-dione is a complex organic compound with the molecular formula C7H8N4O2. It is a derivative of pyrimido[5,4-d]pyrimidine, a fused-ring system consisting of two pyrimidine rings. The compound features a 2-amino group, a 6-methyl group, and two carbonyl groups at the 4 and 8 positions. This molecule is of interest in medicinal chemistry due to its potential as a building block for the synthesis of various biologically active compounds, such as nucleoside analogs and other heterocycles with potential therapeutic applications. Its chemical structure and properties make it a valuable intermediate in the development of new drugs targeting various diseases.

7496-36-8

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7496-36-8 Usage

Properties

1. Chemical Formula: \textC8\textH10\textN4\textO3
2. Structure: Heterocyclic compound with a unique five-membered ring structure.
3. Derivative: Derived from pyrimidine.
4. Common Name: Also known as barbituric acid.
5. Synthesis Usage: Widely used in pharmaceutical synthesis, particularly in the production of barbiturate drugs.
6. Medical Properties: Exhibits sedative, hypnotic, and anticonvulsant properties.
7. Therapeutic Uses: Used in the treatment of anxiety, insomnia, and seizures.
8. Industrial Applications: Employed in the production of dyes and pigments.
9. Versatile Reactivity: Used in the preparation of various organic compounds.

Chemical Structure

The compound consists of a pyrimidine core with an amino group at position 2 and a methyl group at position 6. It also contains two carbonyl groups at positions 4 and 8.

Pharmacological Action

Acts as a central nervous system depressant, producing sedative and hypnotic effects.

Clinical Use

Administered orally, intravenously, or intramuscularly depending on the medical indication.

Barbiturate Drug Production

Serves as a precursor in the synthesis of various barbiturate medications used for their sedative and anesthetic properties.

Therapeutic Applications

Effective in treating anxiety disorders, insomnia, and certain types of seizures.

Dye and Pigment Synthesis

Utilized in the manufacture of various colored compounds, owing to its reactivity with other chemical agents.

Chemical Reactivity

Participates in condensation reactions with urea or urea derivatives, leading to the formation of diverse organic compounds.

Regulatory Status

Subject to control and regulation due to its potential for abuse and addiction.

Toxicity

Overdose can lead to respiratory depression, coma, and death, necessitating careful dosing and monitoring during medical use.

2-amino-6-methyl-1,5-dihydropyrimido[5,4-d]pyrimidine-4,8-dione's diverse properties and applications make it a significant molecule in both pharmaceutical and industrial settings, albeit with associated risks and regulatory considerations.

Check Digit Verification of cas no

The CAS Registry Mumber 7496-36-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7496-36:
(6*7)+(5*4)+(4*9)+(3*6)+(2*3)+(1*6)=128
128 % 10 = 8
So 7496-36-8 is a valid CAS Registry Number.

7496-36-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-6-methyl-1,5-dihydropyrimido[5,4-d]pyrimidine-4,8-dione

1.2 Other means of identification

Product number -
Other names -

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:7496-36-8 SDS

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