129-42-0

  • Product Name:1,8-Diaminoanthraquinone
  • Molecular Formula:C14H10 N2 O2
  • Purity:99%
  • Molecular Weight:238.246
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Product Details;

CasNo: 129-42-0

Molecular Formula: C14H10 N2 O2

Offer Buy High Quality 1,8-Diaminoanthraquinone 129-42-0 On Stock

  • Molecular Formula:C14H10 N2 O2
  • Molecular Weight:238.246
  • Vapor Pressure:3.17E-12mmHg at 25°C 
  • Melting Point:265°C 
  • Refractive Index:1.7570 (estimate) 
  • Boiling Point:551.9°Cat760mmHg 
  • Flash Point:287.6°C 
  • PSA:86.18000 
  • Density:1.456g/cm3 
  • LogP:2.78880 

1,8-diaminoanthraquinone(Cas 129-42-0) Usage

InChI:InChI=1/C14H10N2O2/c15-9-5-1-3-7-11(9)14(18)12-8(13(7)17)4-2-6-10(12)16/h1-6H,15-16H2

129-42-0 Relevant articles

Unique hydrogen bonds between 9-anthracenyl hydrogen and anions

Kwon, Ji Young,Jang, Yun Jung,Kim, Sook Kyung,Lee, Keun-Hyeung,Kim, Jong Seung,Yoon, Juyoung

, p. 5155 - 5157 (2004)

Unique hydrogen bonds of the 9-H of anth...

Human telomerase inhibition by regioisomeric disubstituted amidoanthracene-9,10-diones

Perry, Philip J.,Reszka, Anthony P.,Wood, Alexis A.,Read, Martin A.,Gowan, Sharon M.,Dosanjh, Harvinder S.,Trent, John O.,Jenkins, Terence C.,Kelland, Lloyd R.,Neidle, Stephen

, p. 4873 - 4884 (1998)

Telomerase is an attractive target for t...

Syntheses and structures of hypervalent pentacoordinate carbon and boron compounds bearing an anthracene skeleton - Elucidation of hypervalent interaction based on X-ray analysis and DFT calculation

Yamashita, Makoto,Yamamoto, Yohsuke,Akiba, Kin-Ya,Hashizume, Daisuke,Iwasaki, Fujiko,Takagi, Nozomi,Nagase, Shigeru

, p. 4354 - 4371 (2005)

Pentacoordinate and tetracoordinate carb...

Designed synthesis of ferrocenylanthraquinones and their bifunctional electrochromic properties

Sharmoukh,Ko, Kyoung Chul,Ko, Ju Hong,Jung, Ii Gu,Noh, Changho,Lee, Jin Young,Son, Seung Uk

, p. 3226 - 3229 (2010)

(Figure Presented) New bifunctional elec...

Three anthracene-based bis-imidazolium salts: Synthesis, structure and recognition for 2,4-dinitrophenylhydrazine

Liu, Qingxiang,Yu, Shaocong,Zhao, Zhixiang,Zhang, Xiantao,Liu, Rui

, (2020)

Three anthracene-based bis-imidazolium s...

Anthracene Bisureas as Powerful and Accessible Anion Carriers

Dias, Christopher M.,Valkenier, Hennie,Davis, Anthony P.

, p. 6262 - 6268 (2018)

Synthetic anion carriers (anionophores) ...

Organic cage inclusion crystals exhibiting guest-enhanced multiphoton harvesting

Cooper, Andrew I.,Cui, Peng,Jelfs, Kim E.,Little, Marc A.,Ning, Guo-Hong,Pang, Zhongfu,Pegg, James T.,Sazanovich, Igor V.,Towrie, Mike,Wei, Rong-Jia,Zhu, Qiang

supporting information, p. 3157 - 3170 (2021/11/16)

Host-guest complexation is an important ...

Synthesis, structures and luminescence properties of N^C^N-coordinated platinum(II) complexes based on an anthracene core: A red shift and a twist

Gildea, Louise F.,Williams, J. A. Gareth,Wood, Emily A.,Yufit, Dmitry S.

, (2021/08/07)

1,8-Bis(2-pyridyl)anthracene HL2 is show...

129-42-0 Process route

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

1,8-diamino-anthraquinone
129-42-0

1,8-diamino-anthraquinone

Conditions
Conditions Yield
1,8-dichloroanthraquinone; With copper diacetate; potassium acetate; toluene-4-sulfonamide; air; In nitrobenzene; at 200 ℃; for 5h;
With sulfuric acid; at 100 ℃; for 1h;
58%
Multi-step reaction with 2 steps
1: AcONa, quinoline, copper powder / nitrobenzene / 1 h / 180 - 200 °C
2: 98 percent / concd H2SO4 / 0.75 h / 95 °C
With quinoline; sulfuric acid; sodium acetate; copper; In nitrobenzene;
 
Multi-step reaction with 2 steps
1: 57 percent / Heating
2: 10percent aq. HCl / tetrahydrofuran
With hydrogenchloride; In tetrahydrofuran;
 
Multi-step reaction with 2 steps
2: H2SO4
With sulfuric acid;
 
Multi-step reaction with 2 steps
1: KOAc, Cu(OAc)2 / nitrobenzene
2: aq. H2SO4
With copper diacetate; sulfuric acid; potassium acetate; In nitrobenzene;
 
Multi-step reaction with 2 steps
1: copper diacetate; potassium acetate / pentan-1-ol / 20 h / Reflux
2: sulfuric acid / 2 h / 60 °C
With sulfuric acid; potassium acetate; copper diacetate; In pentan-1-ol;
 
1,8-dinitroanthraquinone
129-39-5

1,8-dinitroanthraquinone

1,8-diamino-anthraquinone
129-42-0

1,8-diamino-anthraquinone

Conditions
Conditions Yield
With sodium sulfide; In ethanol; water; for 12h; Heating;
98%
With sodium sulfide; In ethanol; water; for 64.5h; Reflux;
98%
With sodium sulfide; sodium hydroxide; In ethanol; water; for 6h; Reflux;
98%
With sodium sulfide; sodium hydroxide; In ethanol; water; for 6h; Reflux;
97.5%
With sodiumsulfide nonahydrate; In ethanol; water; for 8h; Reflux;
97%
 
73%
With sodiumsulfide nonahydrate; water; sodium hydroxide; In ethanol; for 6h; Reflux;
73%
With sodium sulfide; In ethanol; for 12h; Reflux;
 
With sodium sulfide; ethanol; sodium hydroxide; for 6h; Reflux;
 
With sodium sulfide; In isopropyl alcohol; for 12h; Inert atmosphere; Reflux;
 
With sodiumsulfide nonahydrate; In water;
 

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