6998-10-3

Basic information

• Product Name: OctanaMide, N-phenyl-
• Synonyms: OctanaMide, N-phenyl-
• CAS NO: 6998-10-3
• Molecular Formula: C₁₄H₂₁NO
• Molecular Weight: 219.32264
• Mol File: 6998-10-3.mol
• Article Data: 30

Chemical Properties

• Melting Point: 49-51 °C
• Boiling Point: 785.3°C at 760 mmHg
• Flash Point: 428.7°C
• Appearance: /
• Density: 1.29g/cm³
• Vapor Pressure: 1.27E-24mmHg at 25°C
• Refractive Index: 1.663
• PKA: 15.17±0.70(Predicted)
• CAS DataBase Reference: OctanaMide, N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: OctanaMide, N-phenyl-(6998-10-3)
• EPA Substance Registry System: OctanaMide, N-phenyl-(6998-10-3)

Safety Data

• Hazardous Substances Data: 6998-10-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C36H34N4O4S2/c1-6-43-28-16-12-24(13-17-28)32-26(21-39(38-32)27-10-8-7-9-11-27)20-30-34(41)40-33(25-14-18-29(45-5)19-15-25)31(35(42)44-22(2)3)23(4)37-36(40)46-30/h7-22,33H,6H2,1-5H3

Upstream product

• 106-32-1 octanoic acid ethyl ester 
• 62-53-3 aniline 
• 111-64-8 n-octanoic acid chloride 
• 14273-09-7 1-ethoxy-1-octyne 
• 1674-37-9 n-octanophenone 
• 98-80-6 phenylboronic acid 
• 124-07-2 Octanoic acid 
• 98-95-3 nitrobenzene 
• 55-21-0 benzamide 
• 103-84-4 Acetanilid 
• 111-27-3 hexan-1-ol 
• 111-11-5 methyl octanate 
• 505-48-6 octane-1,8-dioic acid 
• 1750-36-3 (E)-N-benzylidenebenzenamine 

Downstream Products

• 3007-71-4 N-octylaniline 
• 111-87-5 octanol 
• 62-53-3 aniline 
• 6998-11-4 N-(4-bromophenyl) octanamide 
• 149647-78-9 vorinostat 
• 6797-17-7 2-(heptyl)benzoxazole 
• 1311478-33-7 C₃₆H₅₈N₄O₂ 
• 125781-65-9 [1-Benzotriazol-1-yl-oct-(E)-ylidene]-phenyl-amine 
• 5833-40-9 Octanoyl-phenyl-carbamic acid isopropyl ester 
• 100794-73-8 N-octanoyl-sulfanilyl chloride 

Relevant articles and documents

Aniline-Tetramic Acids from the Deep-Sea-Derived Fungus Cladosporium sphaerospermum L3P3 Cultured with the HDAC Inhibitor SAHA

Four new tetramic acids, cladosins H-K (1-4), and a related known compound, cladodionen (5), were isolated from the culture of the Mariana Trench (depth 6562 m) sediment-derived fungus Cladosporium sphaerospermum L3P3 treated with the histone deacetylase

Visible-light induced one-pot hydrogenation and amidation of nitroaromatics with carboxylic acids over 2D MXene-derived Pt/N-TiO2/Ti3C2

Pt nanoparticles supported on N doped titanium dioxide/titanium carbide (MXene) heterojunctions were employed as photocatalysts for the tandem reactions between aromatic nitro compounds and carboxylic acids to produce amide products. The 3%Pt/N-TiO2/Ti3C2 heterojunction was prepared by in situ grew TiO2 on Ti3C2 nanosheets and then N doped TiO2 with melamine, Pt nanoparticles with 3.3 nm mean diameter well dispersed on N-TiO2/Ti3C2. 3%Pt/N-TiO2/Ti3C2 had excellent amidation activity and chemoselectivity under visible-light irradiation. The elevated catalytic performance of 3%Pt/N-TiO2/Ti3C2 was owing to the improvement in photogenerated electron and hole separation efficiency through charge short-range directional transmission caused by the intimate contact between the TiO2 and the conductive Ti3C2. This direct hydrogenation along with amidation between nitroaromatics and carboxylic acids own actual merits in the amides produce with no harmful byproducts. In situ DRIFTS spectra verified that the amidation activation with visible light irradiation at 25 °C was much faster than heating.

Efficient nitriding reagent and application thereof

The invention discloses an efficient nitriding reagent and application thereof, wherein the nitriding reagent comprises nitrogen oxide, an active agent, a reducing agent and an organic solvent. By applying the nitriding reagent, nitrogen-containing compounds such as amide, nitrile and the like can be produced, and the method is simple in condition, low in waste discharge amount and simple in reaction equipment.