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1,5,7-trimethyl-1H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione is a complex organic compound with the molecular formula C9H10N4O2. It is a derivative of pyrazolo[3,4-d]pyrimidine, a heterocyclic compound with a pyrazole and a pyrimidine ring fused together. The compound is characterized by the presence of three methyl groups (-CH3) attached to the 1st, 5th, and 7th carbon atoms, and two carbonyl groups (C=O) at the 4th and 6th positions. This molecule is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various biologically active compounds. Its unique structure and functional groups make it an interesting target for further research and development in the field of drug discovery and design.

4318-52-9

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4318-52-9 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

A heterocyclic compound is a cyclic compound containing atoms of at least two different elements, in this case, carbon, nitrogen, and oxygen.

Explanation

The core structure refers to the central ring system of the compound, which is a fusion of a pyrazole and a pyrimidine.

Explanation

A dione functional group is characterized by the presence of two carbonyl groups (C=O) within the molecule.

Explanation

The three methyl groups are attached to the 1st, 5th, and 7th positions of the core structure.

Explanation

These properties suggest that the compound may have therapeutic effects in reducing inflammation and pain.

Explanation

The compound's potential pharmacological properties make it a candidate for further research in the development of new drugs targeting various medical conditions, including neurological disorders.

Explanation

The compound can be used as a starting material for the synthesis of other organic compounds, expanding its potential applications in chemistry.

Explanation

More research is required to fully understand the compound's potential uses, properties, and mechanisms of action.

Heterocyclic compound

Yes

Core structure

Pyrazolo[3,4-d]pyrimidine

Functional group

Dione

Position of methyl groups

1, 5, and 7

Potential pharmacological properties

Anti-inflammatory, analgesic

Applications

Medicinal chemistry, drug development, neurological disorders

Synthesis utility

Building block for other organic compounds

Research status

Further research needed

Check Digit Verification of cas no

The CAS Registry Mumber 4318-52-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,1 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4318-52:
(6*4)+(5*3)+(4*1)+(3*8)+(2*5)+(1*2)=79
79 % 10 = 9
So 4318-52-9 is a valid CAS Registry Number.

4318-52-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5,7-trimethylpyrazolo[3,4-d]pyrimidine-4,6-dione

1.2 Other means of identification

Product number -
Other names 1,5,7-Trimethyl-4,6-dioxo-4,5,6,7-tetrahydro-pyrazolo<3,4-d>pyrimidin

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:4318-52-9 SDS

4318-52-9Downstream Products

4318-52-9Relevant academic research and scientific papers

Preparation of pyrazolo[3',4':4,5]pyrido[2,3-d]pyrimidines by the intramolecular reaction of azomethine imines in a 2,4(1H,3H)-pyrimidinedione system

Noguchi,Yamada

, p. 145 - 148 (2007/10/02)

A facile synthetic route to establish 6,8-dimethyl-3,3a,4,5-dihydro-2H-pyrazolo[3',4':4,5]pyrido[2,3- d]pyrimidine-7,9(6H,8H)-diones is described based on an intramolecular azomethine imine cyclization followed by dehydrogenation. The azomethine imine int

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