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16206-19-2

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16206-19-2 Usage

Description

[1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7-diamine 1-oxide is a chemical compound that features an oxadiazole ring and a pyrimidine ring. This potent compound holds potential applications in the fields of medicinal chemistry and drug design. The presence of the 1-oxide functional group, which is an oxygen atom bound to the nitrogen atom at the 1 position of the pyrimidine ring, suggests that it may possess properties suitable for pharmaceutical use. It could potentially function as a bioactive agent or exhibit other therapeutic effects. However, further research and testing are necessary to fully comprehend the compound's potential uses and properties.

Uses

Used in Pharmaceutical Industry:
[1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7-diamine 1-oxide is used as a potential bioactive agent for its possible therapeutic effects. [1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7-diamine 1-oxide's unique structure, which includes an oxadiazole ring and a pyrimidine ring with a 1-oxide functional group, may contribute to its effectiveness in various medicinal applications.
Used in Drug Design:
[1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7-diamine 1-oxide is used as a compound in drug design due to its potential to be developed into new pharmaceuticals. Its structure may allow for the creation of novel drugs with specific therapeutic properties, pending further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 16206-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,0 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16206-19:
(7*1)+(6*6)+(5*2)+(4*0)+(3*6)+(2*1)+(1*9)=82
82 % 10 = 2
So 16206-19-2 is a valid CAS Registry Number.

16206-19-2SDS

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 1-oxido-[1,2,5]oxadiazolo[3,4-d]pyrimidin-1-ium-5,7-diamine

1.2 Other means of identification

Product number -
Other names 1(or 3)-oxy-[1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7-diamine

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:16206-19-2 SDS

16206-19-2Downstream Products

16206-19-2Relevant articles and documents

Facile synthesis and NO-generating property of 4H-[1, 2, 5]oxadiazolo[3, 4-d]pyrimidine-5, 7-dione 1-oxides

Sako, Magoichi,Souichi Oda, Seiji Ohara,Hirota, Kosaku,Maki, Yoshifumi

, p. 6947 - 6951 (2007/10/03)

4H-[1, 2, 5]Oxadiazolo[3, 4-d]pyrimidine-5, 7-dione 1-oxides (2) are conveniently prepared in high yields by the oxidative intramolecular cyclization of 6-amino-5-mtro-lH-pyrimidine-2, 4-diones (1) employing iodosylbenzene diacetate as an oxidant in the presence of lithium hydride. The generation of nitric oxide (NO) and NO-related species from 2 occurs in the presence of thiols such as AT-acetylcysteamine, cysteine, and glutathione under physiological conditions. The evidence for the NO generation derives from mechanistic interpretations for the reaction of 2 with thiols and other chemical observations.

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