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4-[5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]-2-oxobutylidenediazenium (non-preferred name) is a synthetic chemical compound characterized by the presence of a diazenium group and an oxobutylidene group. 4-[5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]-2-oxobutylidenediazenium (non-preferred name) features a pyrimidine ring, a tetrahydrofuran ring, and a butylidene group, which contribute to its unique chemical properties and potential biological activities. Its ability to release nitric oxide, a molecule with various physiological effects, makes it a promising candidate for biomedical applications.

75863-53-5

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75863-53-5 Usage

Uses

Used in Pharmaceutical Applications:
4-[5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]-2-oxobutylidenediazenium (non-preferred name) is used as a potential therapeutic agent for various medical conditions due to its nitric oxide-releasing properties. Nitric oxide plays a crucial role in numerous physiological processes, including vasodilation, immune response, and neurotransmission. 4-[5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]-2-oxobutylidenediazenium (non-preferred name)'s ability to modulate nitric oxide levels may offer therapeutic benefits in treating conditions such as cardiovascular diseases, inflammatory disorders, and neurological disorders.
Used in Research and Development:
In the field of scientific research, 4-[5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]-2-oxobutylidenediazenium (non-preferred name) serves as a valuable tool for studying the mechanisms of action and potential applications of nitric oxide-releasing compounds. Researchers can use {4-[5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]-2-oxobutylidene}diazenium (non-preferred name) to investigate the effects of nitric oxide on cellular processes and signaling pathways, as well as to develop new drugs and therapies targeting nitric oxide-related pathways.
Used in Drug Delivery Systems:
Similar to gallotannin, 4-[5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]-2-oxobutylidenediazenium (non-preferred name) may also benefit from the development of novel drug delivery systems to enhance its applications and efficacy. By employing various organic and metallic nanoparticles as carriers, the compound's delivery, bioavailability, and therapeutic outcomes can be improved, potentially leading to more effective treatments for various medical conditions.
Used in Chemical Synthesis:
The unique structure of 4-[5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]-2-oxobutylidenediazenium (non-preferred name) makes it a potentially useful building block in the synthesis of other complex molecules with diverse applications. Chemists can exploit the compound's reactive functional groups to create new molecules with tailored properties and functions, expanding the scope of its potential uses in various industries, including pharmaceuticals, materials science, and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 75863-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,6 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 75863-53:
(7*7)+(6*5)+(5*8)+(4*6)+(3*3)+(2*5)+(1*3)=165
165 % 10 = 5
So 75863-53-5 is a valid CAS Registry Number.

75863-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-diazonio-4-[5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]but-1-en-2-olate

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:75863-53-5 SDS

75863-53-5Downstream Products

75863-53-5Relevant academic research and scientific papers

Diazomethyl Ketone Derivatives of Pyrimidine Nucleosides

Montgomery, John A.,Thomas, H. Jeanette

, p. 594 - 598 (2007/10/02)

1,5,6,8-Tetradeoxy-8-diazo-β-D-erythro-7-octulofuranosylthymine (20) and 5,6,8-trideoxy-8-diazo-β-D-ribo-7-octulofuranosyluracil (31), pyrimidine nucleosides containing the reactive diazomethyl ketone function, were prepared from thymidine and uridine via

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