129-42-0
- Product Name:1,8-Diaminoanthraquinone
- Molecular Formula:C14H10 N2 O2
- Purity:99%
- Molecular Weight:238.246
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
- 82-43-9
1,8-dichloroanthraquinone
- 129-42-0
1,8-diamino-anthraquinone
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;
|
- 129-39-5
1,8-dinitroanthraquinone
- 129-42-0
1,8-diamino-anthraquinone
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;
|
129-42-0 Upstream products
-
136918-14-4
phthalimide
-
82-43-9
1,8-dichloroanthraquinone
-
33522-40-6
1,8-bis-(toluene-4-sulfonylamino)-anthraquinone
-
209176-56-7
C30H14N2O6
129-42-0 Downstream products
-
60316-43-0
1,8-bis-methylaminoanthraquinone
-
82-43-9
1,8-dichloroanthraquinone
-
83578-92-1
1,8-diamino-2,4,5,7-tetrachloro-anthraquinone
-
63216-87-5
N,N'-(9,10-dioxo-9,10-dihydro-anthracene-1,8-diyl)-bis-oxalamic acid
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