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2,4(1H,3H)-Pyrimidinedione, 6-(aminomethyl)(9CI) is a pyrimidinedione derivative with the molecular formula C6H7N3O2. It features an aminomethyl substituent group at the 6-position, which contributes to its potent biological activity. This versatile chemical compound is known for its potential applications in pharmaceuticals and agrochemicals, as well as its investigation for antitumor and antiviral properties.

20989-02-0

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20989-02-0 Usage

Uses

Used in Pharmaceutical Industry:
2,4(1H,3H)-Pyrimidinedione, 6-(aminomethyl)(9CI) is used as an intermediate in the synthesis of various pharmaceuticals for its potential antitumor and antiviral properties. Its unique structure allows for the development of new drugs targeting cancer and viral infections, such as HIV.
Used in Agrochemical Industry:
In the agrochemical industry, 2,4(1H,3H)-Pyrimidinedione, 6-(aminomethyl)(9CI) serves as a key component in the creation of agrochemicals. Its biological activity makes it a valuable asset in the development of pesticides and other agricultural chemicals to protect crops and enhance yield.
Used in Research and Development:
2,4(1H,3H)-Pyrimidinedione, 6-(aminomethyl)(9CI) is utilized in research and development for its potential applications in various fields. Scientists are investigating its role in the treatment of cancer and HIV, as well as exploring its potential in other therapeutic areas. 2,4(1H,3H)-Pyrimidinedione, 6-(aminomethyl)(9CI)'s unique properties make it an important subject of study for the development of innovative solutions in medicine and agriculture.

Check Digit Verification of cas no

The CAS Registry Mumber 20989-02-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,9,8 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20989-02:
(7*2)+(6*0)+(5*9)+(4*8)+(3*9)+(2*0)+(1*2)=120
120 % 10 = 0
So 20989-02-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H7N3O2/c6-2-3-1-4(9)8-5(10)7-3/h1H,2,6H2,(H2,7,8,9,10)

20989-02-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(aminomethyl)-1H-pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 4-Aminomethyl-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:20989-02-0 SDS

20989-02-0Upstream product

20989-02-0Relevant academic research and scientific papers

Imidazo[1,5-c]pyrimidin-5-ones

-

, (2008/06/13)

Imidazo[1,5-c]pyrimidin-5-ones have been found to have potent bronchodilator activity. Pharmacological methods of using these compounds and pharmaceutical compositions containing these compounds are also disclosed.

Substituted imidazo[1,5-c]pyrimidines

-

, (2008/06/13)

Substituted imidazo[1,5-c]pyrimidines have been found to have potent bronchodilator activity. Pharmacological methods, pharmaceutical compositions and synthetic intermediates are also disclosed.

Synthesis of new uracil derivatives. On the reactability of 4-chloromethyluracil

Klosa

, p. 228 - 231 (2007/10/02)

The synthesis of new uracil derivatives is described. In 4-chloromethyluracil, chlorine can be easily exchanged under mild conditions for amine, aniline, hydrazine, and phenol.

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