• Product Name8-Aminoquinaldine
  • CasNo. 18978-78-4
  • MFC10H10N2
  • MW158.203
  • Purity
  • AppearanceYellow Crystals
  • Packing
  • Contact usInquiry

Product Details

CasNo: 18978-78-4

MF: C10H10N2

Appearance: Yellow Crystals

Reputable factory supply 8-Aminoquinaldine 18978-78-4 in bulk at low price

  • Molecular Formula:C10H10N2
  • Molecular Weight:158.203
  • Appearance/Colour:Yellow Crystals 
  • Vapor Pressure:0.000405mmHg at 25°C 
  • Melting Point:56-58 °C 
  • Refractive Index:1.681 
  • Boiling Point:316.6 °C at 760 mmHg 
  • PKA:pK1: 4.86(+1) (25°C) 
  • Flash Point:171.1 °C 
  • PSA:38.91000 
  • Density:1.169 g/cm3 
  • LogP:2.70660 

8-Aminoquinaldine(Cas 18978-78-4) Usage

Synthesis Reference(s)

Tetrahedron, 52, p. 2937, 1996 DOI: 10.1016/0040-4020(95)01118-8

InChI:InChI=1/C10H10N2/c1-7-5-6-8-3-2-4-9(11)10(8)12-7/h2-6H,11H2,1H3

18978-78-4 Relevant articles

Palladium complexes bearing an N-heterocyclic carbene–sulfonamide ligand for cooligomerization of ethylene and polar monomers

Tao, Wenjie,Wang, Xiaoming,Ito, Shingo,Nozaki, Kyoko

, p. 474 - 477 (2019)

Herein, we report the synthesis of palla...

Primaquine synergises the activity of chloroquine against chloroquine-resistant P. falciparum

Bray, Patrick G.,Deed, Samantha,Fox, Emma,Kalkanidis, Martha,Mungthin, Mathirut,Deady, Leslie W.,Tilley, Leann

, p. 1158 - 1166 (2005)

In recent years, resistance to the antim...

Long-Chain Alkyl-Substituted 1,10-Phenanthrolines as Surfactant Ligands for Transition-Metal Ions. 1. Synthesis of 4- and 4,7-n-Undecyl-Substituted 1,10-Phenanthrolines

Lund, Gary K.,Holt, Smith L.

, p. 227 - 229 (1981)

A convenient synthesis for 4- and 7-n-un...

Planar-locked Ru-PNN catalysts in 1-phenylethanol dehydrogenation

Fanara, Paul M.,MacMillan, Samantha N.,Lacy, David C.

, p. 3628 - 3644 (2020)

Ru-PNN pincer catalysts of the general f...

Development of Improved Amidoquinoline Polyolefin Catalysts with Ultrahigh Molecular Weight Capacity

Fontaine, Philip P.,Ueligger, Steve,Klosin, Jerzy,Hazari, Amaruka,Daller, Joe,Hou, Jianbo

, p. 1354 - 1363 (2015)

A new synthetic route to amidoquinoline ...

Synthesis of mono-and dialkylsubstituted 1,10-Phenanthrolines

Belser, Peter,Bernhard, Stefan,Guerig, Urs

, p. 2937 - 2944 (1996)

Starting from o-anisidine, alkylated 8-h...

Convenient syntheses and preliminary photophysical properties of novel 8-aminoquinoline appended diaza-18-crown-6 ligands

Xue, Guoping,Bradshaw, Jerald S,Dalley, N.Kent,Savage, Paul B,Krakowiak, Krzysztof E,Izatt, Reed M,Prodi, Luca,Montalti, Marco,Zaccheroni, Nelsi

, p. 7623 - 7628 (2001)

Novel 7,16-bis(8-amino-2-quinolinylmethy...

Substitution effect on the one- and two-photon sensitivity of DMAQ "caging" groups

Petit, Morgane,Tran, Christine,Roger, Thomas,Gallavardin, Thibault,Dhimane, Hamid,Palma-Cerda, Francisco,Blanchard-Desce, Mireille,Acher, Francine C.,Ogden, David,Dalko, Peter I.

, p. 6366 - 6369 (2012)

The systematic SAR study of a "caging" g...

Stepwise construction of polysubstituted phenanthroline-based glutamate pockets for lanthanide complexation

Ziessel, Raymond,Weibel, Nicolas,Charbonniere, Loic J.

, p. 3127 - 3133 (2006)

A multi-functionalized ligand, based on ...

Continuous and Selective Hydrogenation of Heterocyclic Nitroaromatics in a Micropacked Bed Reactor

Chen, Xingkun,Duan, Xiaonan,Wang, Xuepeng,Zhang, Jisong

, p. 2100 - 2109 (2021/09/08)

The hydrogenation of heterocyclic nitroa...

NaI/PPh3-Mediated Photochemical Reduction and Amination of Nitroarenes

Qu, Zhonghua,Chen, Xing,Zhong, Shuai,Deng, Guo-Jun,Huang, Huawen

supporting information, p. 5349 - 5353 (2021/07/21)

A mild transition-metal- and photosensit...

Method for reducing aromatic nitro into arylamine

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Paragraph 0201-0204; 0253-0256; 0293-0296, (2020/07/15)

The invention relates to a method for re...

18978-78-4 Process route

8-nitroquinaldine
881-07-2

8-nitroquinaldine

2-methyl-8-aminoquinoline
18978-78-4

2-methyl-8-aminoquinoline

Conditions
Conditions Yield
With hydrogen; palladium 10% on activated carbon; In ethanol; for 2h;
99%
With 10 wt% Pd(OH)2 on carbon; hydrogen; In ethanol; for 5h;
99%
With hydrogen; In tetrahydrofuran; at 60 ℃; under 15001.5 Torr; Flow reactor;
99.7%
With tetrahydroxydiboron; 5%-palladium/activated carbon; water; In acetonitrile; at 50 ℃; for 24h;
97%
With tetrahydroxydiboron; palladium on activated charcoal; water; In acetonitrile; at 50 ℃; for 24h; Reagent/catalyst; Temperature; Inert atmosphere;
97%
With hydrazine hydrate; palladium on activated charcoal; In methanol; for 3h; Heating;
95%
With hydrogen; palladium on activated charcoal;
95%
With hydrogen iodide; at 90 ℃; for 2h;
95%
With hydrogenchloride; iron; In ethanol; water; acetic acid; for 0.333333h; Reflux;
93%
With tetrahydroxydiboron; copper diacetate; In acetonitrile; at 80 ℃; for 24h; chemoselective reaction; Schlenk technique;
90%
With tris(bipyridine)ruthenium(II) dichloride hexahydrate; ascorbic acid; In methanol; water; at 20 ℃; for 3.5h; chemoselective reaction; Schlenk technique; Inert atmosphere; Irradiation; Green chemistry;
90%
8-nitroquinaldine; With hydrogen iodide; In water; at 90 ℃; for 2h;
With sodium hydrogencarbonate; In water; at 20 ℃;
89%
With ethanol; acetic acid; for 4h; Reflux;
88%
With iron; acetic acid;
83%
With hydrogen; palladium(II) hydroxide;
80%
With iron(III) chloride hexahydrate; hydrazine hydrate; In methanol; Reflux;
68%
With phenylsilane; triphenylphosphine; sodium iodide; In chloroform; at 60 ℃; for 72h; Inert atmosphere; Irradiation;
62%
With tetrahydroxydiboron; water; at 80 ℃; for 8h;
52%
With ammonium sulfide; In ethanol; for 2h; Heating;
45%
With hydrogenchloride; tin(ll) chloride;
With methanol; nickel; Hydrogenation;
With hydrogen; palladium on activated charcoal; In ethanol; at 20 ℃;
With palladium on activated charcoal; hydrogen; In 1,4-dioxane; for 12h;
With tin(ll) chloride; Acidic conditions;
With palladium 10% on activated carbon; hydrogen; In 1,4-dioxane; for 12h;
With tin(ll) chloride; In ethanol; at 70 ℃; for 0.5h; Inert atmosphere;
With tin(ll) chloride; In ethanol; at 70 ℃; for 0.5h; Inert atmosphere;
With 5%-palladium/activated carbon; hydrogen; In ethanol; at 50 ℃; for 4h; under 760.051 Torr; Inert atmosphere;
8-chloroquinaldine
3033-82-7

8-chloroquinaldine

2-methyl-8-aminoquinoline
18978-78-4

2-methyl-8-aminoquinoline

Conditions
Conditions Yield
With ammonium hydroxide; potassium phosphate; copper(l) iodide; N1,N2-bis(5-methyl-[1,1'-biphenyl]-2-yl)oxalamide; In water; dimethyl sulfoxide; at 120 ℃; for 24h; Inert atmosphere;
78%

18978-78-4 Upstream products

  • 826-81-3
    826-81-3

    2-methyl-8-quinolinol

  • 57-13-6
    57-13-6

    urea

  • 881-07-2
    881-07-2

    8-nitroquinaldine

  • 88-74-4
    88-74-4

    2-nitro-aniline

18978-78-4 Downstream products

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    2.9-dimethyl-1,10-phenanthroline

  • 3002-77-5
    3002-77-5

    2-methyl-1,10-phenanthroline

  • 15011-27-5
    15011-27-5

    2-methyl-8-mesitylenesulfonamidoquinoline

  • 118380-05-5
    118380-05-5

    2-(4-Acetylamino-phenyl)-N-(2-methyl-quinolin-8-yl)-acetamide

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