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22294-57-1

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22294-57-1 Usage

General Description

2-Amino-5-iodo-6-methyl-4-pyrimidinol is a chemical compound formulated with the molecular formula C5H6IN3O. Structurally, it consists of a pyrimidinol ring, a type of heterocyclic compound, which is derived from pyrimidine with a hydroxyl (-OH) substituent. The particular compound is characterized by an amino (-NH2) group, an iodine atom, and a methyl (-CH3) group attached to the pyrimidinol ring at positions 2, 5 and 6 respectively. 2-Amino-5-iodo-6-methyl-4-pyrimidinol is used in the field of organic synthesis, functioning as an important intermediate in the chemical industry. However, its specific uses and properties such as reactivity, toxicity, and potential applications in medication or other industries require further investigation and documentation.

Check Digit Verification of cas no

The CAS Registry Mumber 22294-57-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,9 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22294-57:
(7*2)+(6*2)+(5*2)+(4*9)+(3*4)+(2*5)+(1*7)=101
101 % 10 = 1
So 22294-57-1 is a valid CAS Registry Number.

22294-57-1SDS

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 2-amino-5-iodo-6-methyl-1H-pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names aminoiodomethylpyrimidinol

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:22294-57-1 SDS

22294-57-1Relevant articles and documents

Synthesis and biological activity of the 2-amino-4-(4-iodophenyl)amino-6- methylpyrimidine isosteric analogs

Erkin,Krutikov

, p. 538 - 541 (2013/08/23)

Transformation of the structure of 6-methylisocytosine results in the isosteric analogs of 2-amino-4-(4-iodophenyl)amino-6-methylpyrimidine exhibiting tuberculocidal properties. The level of biological activity of the synthesized compounds depends on the

Interferon induction

-

, (2008/06/13)

A method and therapeutic compositions for inducing interferon formation in vivo. To a host is administered an interferon inducer of the formula: SPC1 Wherein X is a member selected from the group consisting of bromo and iodo and Y is a member selected from the group consisting of methyl and ethyl when X is bromo; or Y is a member selected from the group consisting of methyl, ethyl, n-propyl, benzyl and chloro when X is iodo.

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