67015-08-1

Basic information

• Product Name: 2-DIMETHYLAMINO-N-HYDROXY-ACETAMIDINE
• Synonyms: 2-DIMETHYLAMINO-N-HYDROXY-ACETAMIDINE;(1Z)-2-(dimethylamino)-N'-hydroxyethanimidamide(SALTDATA: FREE);(Z)-2-(diMethylaMino)-N'-hydroxyacetiMidaMide;2-(Dimethylamino)-N-hydroxyacetimidamide
• CAS NO: 67015-08-1
• Molecular Formula: C₄H₁₁N₃O
• Molecular Weight: 117.15
• Product Categories: pharmacetical
• Mol File: 67015-08-1.mol

Chemical Properties

• Boiling Point: 226.9 °C at 760 mmHg
• Flash Point: 91 °C
• Appearance: /
• Density: 1.12 g/cm³
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-DIMETHYLAMINO-N-HYDROXY-ACETAMIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-DIMETHYLAMINO-N-HYDROXY-ACETAMIDINE(67015-08-1)
• EPA Substance Registry System: 2-DIMETHYLAMINO-N-HYDROXY-ACETAMIDINE(67015-08-1)

Safety Data

• Hazardous Substances Data: 67015-08-1(Hazardous Substances Data)

Usage

Uses

Given the limited information on the specific applications of 2-Dimethylamino-N-hydroxy-acetamidine, the following uses are inferred based on its classification as an organic compound and general practices in the chemical and biological fields:
Used in Chemical Research:
2-Dimethylamino-N-hydroxy-acetamidine is used as a research chemical for exploring its properties and potential reactions with other compounds. This can contribute to the development of new chemical processes or the synthesis of novel molecules.
Used in Biological Studies:
In biological research, 2-Dimethylamino-N-hydroxy-acetamidine may serve as a starting material or intermediate in the synthesis of biologically active molecules, potentially leading to the discovery of new pharmaceutical agents or tools for biological investigations.
Used in Material Science:
2-DIMETHYLAMINO-N-HYDROXY-ACETAMIDINE could be employed in material science applications, such as the development of new polymers or materials with specific properties,得益于其独特的化学结构和潜在的反应性。

Upstream product

• 926-64-7 N,N-Dimethylamino acetonitrile 

Downstream Products

• 1009621-06-0 (3-dimethylaminomethyl-[1,2,4]oxadiazole-5-yl)-phenyl-methanone 

Relevant articles and documents

Novel O-acylated amidoximes and substituted 1,2,4-oxadiazoles synthesised from (+)-ketopinic acid possessing potent virus-inhibiting activity against phylogenetically distinct influenza A viruses

This article describes the synthesis and antiviral activity evaluation of new substituted 1,2,4-oxadiazoles containing a bicyclic substituent at position 5 of the heterocycle and O-acylated amidoximes as precursors for their synthesis. New compounds were

MORPHOLINE DERIVATIVES, COMPOSITIONS CONTAINING THEM AND THEIR USE AS THERAPEUTIC AGENTS

The present invention relates to compounds of formula (I), wherein R. sup.1 and R 4 represent hydrogen, halogen, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-7 cycloalkyl, C 3-7 cycloalkylC. sub.1-4 alkyl, C 1-6 alkoxy, C 1-4 alkyl substituted by a hydroxy or C 1-4 alkoxy group, OCF 3, hydroxy, trifluoromethyl, trimethylsilyl, nitro, CN, SR a, SOR a, SO 2 R a, COR. sup.a, CO 2 R a or CONR a R b, where R. sup.a and R b are each independently hydrogen or C 1-4 alkyl; R. sup.2, R 3 and R 5 represent hydrogen, halogen, C 1-6 alkyl, C 1-4 alkoxy substituted by a C 1-4 alkoxy group, or trifluoromethyl; R 6 represents C 1-6 alkyl, optionally substituted by oxo, substituted by a 5-membered heteroaromatic ring selected from oxazole, thiazole, isoxazole, isothiazole, oxadiazole and thiadiazole, wherein each heteroaromatic ring is substituted at the available carbon atom by a group of the formula: ZNR 7 R 8. The compounds are of particular use in the treatment of pain, inflammation, migraine and emesis.