59417-06-0

Basic information

• Product Name: SALOR-INT L169811-1EA
• Synonyms: SALOR-INT L169811-1EA;1,4-DIMETHYL-2,3-PIPERAZINEDIONE;1,4-DIMETHYLPIPERAZINE-2,3-DIONE
• CAS NO: 59417-06-0
• Molecular Formula: C₆H₁₀N₂O₂
• Molecular Weight: 142.16
• Mol File: 59417-06-0.mol
• Article Data: 13

Chemical Properties

• Melting Point: 176-179 °C
• Boiling Point: 206.5 °C at 760 mmHg
• Flash Point: 81.2 °C
• Appearance: /
• Density: 1.169 g/cm³
• Vapor Pressure: 0.237mmHg at 25°C
• Refractive Index: 1.491
• Storage Temp.: 2-8°C
• PKA: -1.19±0.20(Predicted)
• CAS DataBase Reference: SALOR-INT L169811-1EA(CAS DataBase Reference)
• NIST Chemistry Reference: SALOR-INT L169811-1EA(59417-06-0)
• EPA Substance Registry System: SALOR-INT L169811-1EA(59417-06-0)

Safety Data

• Hazardous Substances Data: 59417-06-0(Hazardous Substances Data)

Usage

General Description

The chemical compound "SALOR-INT L169811-1EA" is not specific enough to provide a detailed summary. Without more information about the specific characteristics and composition of this compound, it is not possible to provide a concise summary. It is important to know the chemical formula, physical and chemical properties, and potential uses of the compound in order to provide a meaningful summary.

InChI:InChI=1/C6H10N2O2/c1-7-3-4-8(2)6(10)5(7)9/h3-4H2,1-2H3

Upstream product

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Relevant articles and documents

Visible light promoted continuous flow photocyclization of 1,2-diketones

The continuous flow Norrish-Yang photocyclization of 1,2-diketones has been developed and used for the synthesis of a large number of functionalized 2-hydroxycyclobutanones, under blue light irradiation and employing acetone as a solvent. This eco-friendly procedure represents a valid alternative to the reactions carried out in batches thus reducing the reaction times, the formation of secondary products and simplifying the purification steps. The use of differently substituted diketone compounds has allowed us to obtain a wide range of 2 and 3-functionalized cyclobutanones, thus allowing the evaluation of the scope and limitations of this procedure.

PIDA/I2-Mediated α- And β-C(sp3)-H Bond Dual Functionalization of Tertiary Amines

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A series of new quinoxaline-based thiophene copolymers (PQx2T, PQx4T, and PQx6T) was synthesized via Yamamoto and Stille coupling reactions. The M ws of PQx2T, PQx4T, and PQx6T were found to be 20,000, 12,000, and 29,000, with polydispersity in