163032-70-0

Basic information

• Product Name: NOR-1
• Synonyms: -((E)-hydroxyimino)-6-*methoxy-4-methyl;(+/-)-(E)-METHYL-2-[(E)-HYDROXYIMINO]-5-NITRO-6-METHOXY-3-HEXENEAMIDE;NOR-1;(+-)-(E)-2-((E)-hydroxyimino)-6-*methoxy-4-methyl;(+or-)-(E)4-Methyl-2-[(E)-hydroxyimino]-5-nitro-6-methoxy-3-hexenamide;(±)-(E)-2-[(E)-Hydroxyimino]-6-methoxy-4-methyl-5-nitro-3-hexenamide
• CAS NO: 163032-70-0
• Molecular Formula: C8H13N3O5
• Molecular Weight: 231.21
• Mol File: 163032-70-0.mol

Chemical Properties

• Boiling Point: 460.6 °C at 760 mmHg
• Flash Point: 232.4 °C
• Appearance: white or slightly yellow powder
• Density: 1.37 g/cm³
• Vapor Pressure: 2.02E-10mmHg at 25°C
• Refractive Index: 1.542
• Storage Temp.: −20°C
• CAS DataBase Reference: NOR-1(CAS DataBase Reference)
• NIST Chemistry Reference: NOR-1(163032-70-0)
• EPA Substance Registry System: NOR-1(163032-70-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• Hazardous Substances Data: 163032-70-0(Hazardous Substances Data)

Usage

Uses

Used in Cardiovascular Disease Research:
NOR-1 is used as a target for therapeutic interventions in cardiovascular diseases, particularly atherosclerosis and heart failure, due to its involvement in the regulation of gene expression and cellular processes related to these conditions.
Used in Skeletal Muscle Research:
NOR-1 is used as a potential target for therapeutic interventions in muscle-wasting conditions and metabolic disorders, as it may play a role in the regulation of skeletal muscle mass and function.
Used in Inflammation and Metabolism Research:
NOR-1 is used as a target for understanding its role in inflammation and metabolism, as it is involved in the regulation of gene expression and cellular processes related to these functions.
Used in Apoptosis and Cell Proliferation Research:
NOR-1 is used as a target for studying its role in apoptosis and cell proliferation, which are essential cellular processes that can have implications in various diseases and conditions.

InChI:InChI=1/C8H13N3O5/c1-5(3-6(10-13)8(9)12)7(4-16-2)11(14)15/h3,7,13H,4H2,1-2H3,(H2,9,12)/b5-3+,10-6-

Upstream product

• 4356-74-5 (E)-4-methoxy-2-methyl-but-2-enal 

Relevant articles and documents

New reagents for controlled release of nitric oxide. Structure-stability relationships

The synthesis and structure-stability relationships of a series of novel FK409 derivatives are described. The rates of decomposition in aqueous solution (pH 8.0, 30°C) were parallel with those of spontaneous NO release measured by ESR spectroscopy using carboxy-PTIO. The compounds can cover a wide range of NO releasing rates by appropriate modification of the molecule.