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82-43-9 Usage

Uses

1,8-Dichloroanthraquinone is a reagent in the preparation of anthraquinones, which has antitumor activities. It is used as primary and secondary intermediate.

Safety Profile

An eye irritant. When heated to decomposition it emits toxic fumes of Cl-.

Check Digit Verification of cas no

The CAS Registry Mumber 82-43-9 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82-43:
(4*8)+(3*2)+(2*4)+(1*3)=49
49 % 10 = 9
So 82-43-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H6Cl2O2/c15-9-5-1-3-7-11(9)14(18)12-8(13(7)17)4-2-6-10(12)16/h1-6H

82-43-9 Well-known Company Product Price

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  • Alfa Aesar

  • (B23421)  1,8-Dichloroanthraquinone, 96%   

  • 82-43-9

  • 25g

  • 464.0CNY

  • Detail
  • Alfa Aesar

  • (B23421)  1,8-Dichloroanthraquinone, 96%   

  • 82-43-9

  • 100g

  • 1663.0CNY

  • Detail
  • Alfa Aesar

  • (B23421)  1,8-Dichloroanthraquinone, 96%   

  • 82-43-9

  • 500g

  • 8009.0CNY

  • Detail

82-43-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,8-Dichloroanthraquinone

1.2 Other means of identification

Product number -
Other names 9,10-Anthracenedione, 1,8-dichloro-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:82-43-9 SDS

82-43-9Synthetic route

1,8-anthraquinonedisulphonic acid
82-48-4

1,8-anthraquinonedisulphonic acid

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

Conditions
ConditionsYield
With hydrogenchloride Irradiation;
With hydrogenchloride; sodium chlorate at 100℃;
1,8-diamino-anthraquinone
129-42-0

1,8-diamino-anthraquinone

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

Conditions
ConditionsYield
With hydrogenchloride; sodium nitrite Diazotization.man erhitzt die erhaltene Diazoniumchloridloesung auf 100grad;
anthracene-1,8-disulphonic acid
61736-92-3

anthracene-1,8-disulphonic acid

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

Conditions
ConditionsYield
With hydrogenchloride; sodium chlorate at 100℃;
hydrogenchloride
7647-01-0

hydrogenchloride

1,8-anthraquinonedisulphonic acid
82-48-4

1,8-anthraquinonedisulphonic acid

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

Conditions
ConditionsYield
mit Sonnenlicht.Irradiation;
8-chloro-9,10-dioxo-9,10-dihydro-anthracene-1-sulfonic acid
41125-15-9

8-chloro-9,10-dioxo-9,10-dihydro-anthracene-1-sulfonic acid

water
7732-18-5

water

chlorine
7782-50-5

chlorine

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

Conditions
ConditionsYield
at 94℃; Kinetics;
at 104℃; Kinetics;
potassium salt of/the/ anthraquinone-disulfonic acid-(1.8)

potassium salt of/the/ anthraquinone-disulfonic acid-(1.8)

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

Conditions
ConditionsYield
With tetrachloromethane; thionyl chloride at 170℃;
hydrogenchloride
7647-01-0

hydrogenchloride

1,8-anthraquinonedisulphonic acid
82-48-4

1,8-anthraquinonedisulphonic acid

sodium perchlorate

sodium perchlorate

A

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

B

8-chloro-9,10-dioxo-9,10-dihydro-anthracene-1-sulfonic acid
41125-15-9

8-chloro-9,10-dioxo-9,10-dihydro-anthracene-1-sulfonic acid

Conditions
ConditionsYield
at 100℃; reagiert analog mit Brom und Wasser beim Erhitzen im Rohr;
tetrachloromethane
56-23-5

tetrachloromethane

thionyl chloride
7719-09-7

thionyl chloride

anthracene-1,8-disulphonic acid
61736-92-3

anthracene-1,8-disulphonic acid

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

Conditions
ConditionsYield
at 170℃; Reaktion des Kaliumsalzes;
hydrogenchloride
7647-01-0

hydrogenchloride

anthracene-1,8-disulphonic acid
61736-92-3

anthracene-1,8-disulphonic acid

sodium perchlorate

sodium perchlorate

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

Conditions
ConditionsYield
at 100℃;
1,5-anthraquinone disulfonate
117-14-6

1,5-anthraquinone disulfonate

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: sulfuric acid; mercury
2: mercury oxide / Darst;bei der Sulfurierung
3: diluted hydrochloric acid; sodium chlorate / 100 °C
View Scheme
Multi-step reaction with 5 steps
1: sulfuric acid; mercury
2: mercury oxide / Darst;ueber mehrere Stufen
3: sulfuric acid; mercury
4: mercury oxide / Darst;bei der Sulfurierung
5: diluted hydrochloric acid; sodium chlorate / 100 °C
View Scheme
1-anthraquinonesulfonic acid
82-49-5

1-anthraquinonesulfonic acid

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: sulfuric acid; mercury
2: mercury oxide / Darst;bei der Sulfurierung
3: diluted hydrochloric acid; sodium chlorate / 100 °C
View Scheme
Multi-step reaction with 5 steps
1: sulfuric acid; mercury
2: mercury oxide / bei der Sulfurierung
3: sulfuric acid; mercury
4: mercury oxide / Darst;bei der Sulfurierung
5: diluted hydrochloric acid; sodium chlorate / 100 °C
View Scheme
9,10-phenanthrenequinone
84-65-1

9,10-phenanthrenequinone

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: mercury oxide / Darst;bei der Sulfurierung
2: diluted hydrochloric acid; sodium chlorate / 100 °C
View Scheme
Multi-step reaction with 4 steps
1: mercury oxide / bei der Sulfurierung
2: sulfuric acid; mercury
3: mercury oxide / Darst;bei der Sulfurierung
4: diluted hydrochloric acid; sodium chlorate / 100 °C
View Scheme
Multi-step reaction with 6 steps
1: mercury oxide / bei der Sulfurierung
2: sulfuric acid; mercury
3: mercury oxide / Darst;ueber mehrere Stufen
4: sulfuric acid; mercury
5: mercury oxide / Darst;bei der Sulfurierung
6: diluted hydrochloric acid; sodium chlorate / 100 °C
View Scheme
Multi-step reaction with 4 steps
1: mercury oxide / Darst;ueber mehrere Stufen
2: sulfuric acid; mercury
3: mercury oxide / Darst;bei der Sulfurierung
4: diluted hydrochloric acid; sodium chlorate / 100 °C
View Scheme
Multi-step reaction with 6 steps
1: mercury oxide / Darst;ueber mehrere Stufen
2: sulfuric acid; mercury
3: mercury oxide / bei der Sulfurierung
4: sulfuric acid; mercury
5: mercury oxide / Darst;bei der Sulfurierung
6: diluted hydrochloric acid; sodium chlorate / 100 °C
View Scheme
1-chloroanthracene-9,10-dione
82-44-0

1-chloroanthracene-9,10-dione

2-chloroanthracene-9,10-dione
131-09-9

2-chloroanthracene-9,10-dione

A

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

B

1,4,8-Trichloroanthraquinone
1594-64-5

1,4,8-Trichloroanthraquinone

Conditions
ConditionsYield
In aqueous sodium chlorate
1,8-dichloro-9,10-dihydroxyanthracene
86190-38-7

1,8-dichloro-9,10-dihydroxyanthracene

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

Conditions
ConditionsYield
With cobalt(III) phosphide In tetrahydrofuran-d8 at 20 - 50℃; for 144h; Catalytic behavior;
hexan-1-amine
111-26-2

hexan-1-amine

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

1,8-bis(hexylamino)anthraquinone
123296-37-7

1,8-bis(hexylamino)anthraquinone

Conditions
ConditionsYield
With caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; bis(dibenzylideneacetone)-palladium(0) In 1,4-dioxane for 24h; Heating;98%
In N,N-dimethyl-formamide for 0.5h; Heating;52%
In dimethyl sulfoxide for 0.25h; Heating;50%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

aniline
62-53-3

aniline

1,8-bis(Phenylamino)anthraquinone
2944-26-5

1,8-bis(Phenylamino)anthraquinone

Conditions
ConditionsYield
With 1,1'-bis-(diphenylphosphino)ferrocene; caesium carbonate; bis(dibenzylideneacetone)-palladium(0) In 1,4-dioxane for 24h; Heating;98%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

4-Ethoxyaniline
156-43-4

4-Ethoxyaniline

1,8-bis(4-ethoxyphenylamino)anthraquinone

1,8-bis(4-ethoxyphenylamino)anthraquinone

Conditions
ConditionsYield
With caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; bis(dibenzylideneacetone)-palladium(0) In 1,4-dioxane for 24h; Heating;98%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

4,5-dichloro-10-hydroxyanthracen-9(10H)-one
63605-25-4

4,5-dichloro-10-hydroxyanthracen-9(10H)-one

Conditions
ConditionsYield
With sodium dithionite In water; N,N-dimethyl-formamide at 20℃; Inert atmosphere; Schlenk technique;98%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

4,5-dichloro-10H-anthracen-9-one
63605-29-8

4,5-dichloro-10H-anthracen-9-one

Conditions
ConditionsYield
With sodium dithionite In water; N,N-dimethyl-formamide at 30 - 90℃; for 4.5h; Inert atmosphere; Schlenk technique;96%
Stage #1: 1,8-dichloroanthraquinone With sodium tetrahydroborate In methanol for 6h;
Stage #2: With hydrogenchloride In methanol for 1h; Reflux;
89%
Stage #1: 1,8-dichloroanthraquinone With sodium tetrahydroborate In methanol at -78 - 20℃; for 3.5h; Inert atmosphere; Schlenk technique;
Stage #2: With hydrogenchloride In methanol; water Reflux; Inert atmosphere; Schlenk technique;
88%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

p-toluidine
106-49-0

p-toluidine

1,8-bis(p-tolylamino)anthraquinone
82-16-6

1,8-bis(p-tolylamino)anthraquinone

Conditions
ConditionsYield
With caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; bis(dibenzylideneacetone)-palladium(0) In 1,4-dioxane for 24h; Heating;95%
With sodium acetate; sodium carbonate at 190 - 195℃;
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

(9r,10r)-1,8-dichloro-9,10-dihydroanthracene-9,10-diol
50259-86-4

(9r,10r)-1,8-dichloro-9,10-dihydroanthracene-9,10-diol

Conditions
ConditionsYield
With methanol; sodium tetrahydroborate at 0 - 5℃; for 3h; Inert atmosphere; Schlenk technique;90%
With sodium tetrahydroborate In methanol
With sodium tetrahydroborate
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

(9s,10s)-1,8-dichloro-9,10-dihydroanthracene-9,10-diol
50259-86-4, 73274-95-0

(9s,10s)-1,8-dichloro-9,10-dihydroanthracene-9,10-diol

Conditions
ConditionsYield
Stage #1: 1,8-dichloroanthraquinone With diisobutylaluminium hydride In tetrahydrofuran; hexane at 20℃; for 5h;
Stage #2: With rochelle salt In tetrahydrofuran; hexane; water at 20℃; for 16h;
89%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

1,8-dichloroanthracene
14381-66-9

1,8-dichloroanthracene

Conditions
ConditionsYield
With ammonium hydroxide; copper(II) sulfate; zinc at 80℃; for 4.5h;88%
Stage #1: 1,8-dichloroanthraquinone With ammonium hydroxide; zinc at 80℃; for 5h; Inert atmosphere;
Stage #2: With hydrogenchloride In isopropyl alcohol Inert atmosphere;
88%
With ammonium hydroxide; zinc at 75℃; for 4h;84.7%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

(3α,5β)-3-hydroxycholan-24-amine
90595-86-1

(3α,5β)-3-hydroxycholan-24-amine

1,8-bis[(3α,5β)-3-hydroxycholan-24-ylamino]-9,10-anthraquinone

1,8-bis[(3α,5β)-3-hydroxycholan-24-ylamino]-9,10-anthraquinone

Conditions
ConditionsYield
With 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; bis(dibenzylideneacetone)-palladium(0); sodium t-butanolate In 1,4-dioxane at 100℃; for 24h; Buchwald-Hartwig Coupling; Inert atmosphere;88%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

A

1,8-dichloro-9,10-dihydroanthracen-9-one
50259-93-3

1,8-dichloro-9,10-dihydroanthracen-9-one

B

4,5-dichloro-10H-anthracen-9-one
63605-29-8

4,5-dichloro-10H-anthracen-9-one

Conditions
ConditionsYield
With sulfuric acid; aluminium at 25 - 30℃; for 8h;A 86%
B n/a
With tin(ll) chloride In hydrogenchloride; acetic acid for 5h; Heating;A 35%
B 50%
With hydrogenchloride; tin(II) chloride dihdyrate; acetic acid In water for 3h; Reflux; Inert atmosphere;A 23.8%
B 37.4%
With hydrogenchloride; tin; acetic acid
With hydrogenchloride; acetic acid; tin(ll) chloride In water at 120℃; for 12h; Overall yield = 80 percent; Overall yield = 7.5 g;
4-(2-AMINOETHYL)MORPHOLINE
2038-03-1

4-(2-AMINOETHYL)MORPHOLINE

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

1,8-bis-(2-morpholin-4-yl-ethylamino)-anthraquinone
3924-55-8

1,8-bis-(2-morpholin-4-yl-ethylamino)-anthraquinone

Conditions
ConditionsYield
In dimethyl sulfoxide for 0.25h; Heating;85%
(2-hydroxyethyl)(methyl)amine
109-83-1

(2-hydroxyethyl)(methyl)amine

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

1,8-bis((2-hydroxyethyl)(methyl)amino)-9,10-anthraquinone
345265-61-4

1,8-bis((2-hydroxyethyl)(methyl)amino)-9,10-anthraquinone

Conditions
ConditionsYield
With triethylamine In toluene at 120℃; for 72h; Inert atmosphere;85%
propylamine
107-10-8

propylamine

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

1,8-bis(propylamine)-anthraquinone

1,8-bis(propylamine)-anthraquinone

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 0.5h; Heating;83%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

ethanolamine
141-43-5

ethanolamine

1,8-bis-(2-hydroxy-ethylamino)-anthraquinone
75312-66-2

1,8-bis-(2-hydroxy-ethylamino)-anthraquinone

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 0.5h; Heating;80%
2-(aminoethyl)pyridine
2706-56-1

2-(aminoethyl)pyridine

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

1,8-bis[2-(2'-pyridinyl)ethylamino]-9,10-anthracenedione
123296-41-3

1,8-bis[2-(2'-pyridinyl)ethylamino]-9,10-anthracenedione

Conditions
ConditionsYield
In dimethyl sulfoxide for 0.25h; Heating;80%
In dimethyl sulfoxide at 150℃; for 0.166667h; Substitution;30%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

ethanolamine
141-43-5

ethanolamine

1-Chloro-8-(2-hydroxy-ethylamino)-anthraquinone

1-Chloro-8-(2-hydroxy-ethylamino)-anthraquinone

Conditions
ConditionsYield
In pyridine for 12h; Heating;80%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

Trimethylenediamine
109-76-2

Trimethylenediamine

1,8-bis[(3-aminopropyl)amino]anthraquinone
87075-42-1

1,8-bis[(3-aminopropyl)amino]anthraquinone

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 0.5h; Heating;80%
With tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate In acetonitrile for 12h; Reflux;80%
In dimethyl sulfoxide for 0.25h; Heating;70%
With caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; bis(dibenzylideneacetone)-palladium(0) In 1,4-dioxane for 24h; Heating;48%
In dimethyl sulfoxide at 150℃; for 4h; Schlenk technique; Inert atmosphere;23%
morpholine
110-91-8

morpholine

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

1,8-dimorpholinoanthraquinone

1,8-dimorpholinoanthraquinone

Conditions
ConditionsYield
With caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; bis(dibenzylideneacetone)-palladium(0) In 1,4-dioxane for 24h; Heating;79%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

diphenyl diselenide
1666-13-3

diphenyl diselenide

1,8-bis(phenylselanyl)anthraquinone

1,8-bis(phenylselanyl)anthraquinone

Conditions
ConditionsYield
Stage #1: diphenyl diselenide With sodium tetrahydroborate In ethanol; N,N-dimethyl-formamide; benzene at 110℃;
Stage #2: 1,8-dichloroanthraquinone With copper(l) iodide In ethanol; N,N-dimethyl-formamide; benzene for 20h; Heating;
78%
Stage #1: diphenyl diselenide With sodium tetrahydroborate In ethanol; N,N-dimethyl-formamide; benzene at 110℃;
Stage #2: 1,8-dichloroanthraquinone With copper(l) iodide In ethanol; N,N-dimethyl-formamide; benzene for 20h; Heating; Further stages.;
78%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

1,3-Diamino-2-hydroxypropane
616-29-5

1,3-Diamino-2-hydroxypropane

C20H24N4O4

C20H24N4O4

Conditions
ConditionsYield
In dimethyl sulfoxide at 150℃; for 4h; Schlenk technique; Inert atmosphere;78%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

phenol
108-95-2

phenol

A

C20H11ClO3

C20H11ClO3

B

1,8-diphenoxyanthracene-9,10-dione
82-17-7

1,8-diphenoxyanthracene-9,10-dione

Conditions
ConditionsYield
With copper; potassium hydroxide at 130℃; for 2h;A n/a
B 77%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

sodium 3-mercaptopropanesulfonate
17636-10-1

sodium 3-mercaptopropanesulfonate

C20H18O8S4(2-)*2Na(1+)

C20H18O8S4(2-)*2Na(1+)

Conditions
ConditionsYield
With sodium hydroxide In 1-methyl-pyrrolidin-2-one; water at 90℃; for 144h;77%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

phenylboronic acid
98-80-6

phenylboronic acid

1,8-Diphenyl-9,10-anthrachinon
33522-27-9

1,8-Diphenyl-9,10-anthrachinon

Conditions
ConditionsYield
With bis(tri-t-butylphosphine)palladium(0); potassium carbonate In 1,4-dioxane; water for 24h; Reflux;76.8%
phthalimide
136918-14-4

phthalimide

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

C30H14N2O6
209176-56-7

C30H14N2O6

Conditions
ConditionsYield
With quinoline; sodium acetate; copper In nitrobenzene at 180 - 200℃; for 1h;76%
With quinoline; sodium acetate; copper In nitrobenzene at 180 - 200℃; for 1h;
1-(2-aminoethyl)pyrrolidine
7154-73-6

1-(2-aminoethyl)pyrrolidine

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

1,8-Bis-(2-pyrrolidin-1-yl-ethylamino)-anthraquinone
123296-39-9

1,8-Bis-(2-pyrrolidin-1-yl-ethylamino)-anthraquinone

Conditions
ConditionsYield
In dimethyl sulfoxide for 0.25h; Heating;75%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

bis(pinacol)diborane
73183-34-3

bis(pinacol)diborane

C26H30B2O6

C26H30B2O6

Conditions
ConditionsYield
With tris-(dibenzylideneacetone)dipalladium(0); potassium acetate; XPhos In 1,4-dioxane for 24h; Miyaura Borylation Reaction; Glovebox; Inert atmosphere; Sealed tube;75%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

isopropylamine
75-31-0

isopropylamine

1,8-bis(isopropylamine)-anthraquinone

1,8-bis(isopropylamine)-anthraquinone

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 0.5h; Heating;74%
dichloromethane
75-09-2

dichloromethane

1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

(3R,5R,8R,9S,10S,12S,13R,14S,17R)-17-(5-aminopentan-2-yl)-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthrene-3,12-diol
86679-01-8

(3R,5R,8R,9S,10S,12S,13R,14S,17R)-17-(5-aminopentan-2-yl)-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthrene-3,12-diol

1,8-bis[(3α,5β,12α)-3,12-dihydroxycholan-24-ylamino]-9,10-anthraquinone

1,8-bis[(3α,5β,12α)-3,12-dihydroxycholan-24-ylamino]-9,10-anthraquinone

Conditions
ConditionsYield
Stage #1: 1,8-dichloroanthraquinone; (3R,5R,8R,9S,10S,12S,13R,14S,17R)-17-(5-aminopentan-2-yl)-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthrene-3,12-diol With caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; bis(dibenzylideneacetone)-palladium(0) In 1,4-dioxane at 100℃; for 24h; Buchwald-Hartwig Coupling; Inert atmosphere;
Stage #2: dichloromethane In water at 20℃; Inert atmosphere;
74%
1,8-dichloroanthraquinone
82-43-9

1,8-dichloroanthraquinone

1,8-difluoroanthraquinone
361-33-1

1,8-difluoroanthraquinone

Conditions
ConditionsYield
With cesium fluoride In dimethyl sulfoxide at 137℃; for 14h;71%
With cesium fluoride In dimethyl sulfoxide at 135℃; for 10h;60%
With potassium fluoride

82-43-9Relevant articles and documents

Hydrogen on Cobalt Phosphide

Delley, Murielle F.,Wu, Zishan,Mundy, M. Elizabeth,Ung, David,Cossairt, Brandi M.,Wang, Hailiang,Mayer, James M.

, p. 15390 - 15402 (2019/11/02)

Cobalt phosphide (CoP) is one of the most promising earth-abundant replacements for noble metal catalysts for the hydrogen evolution reaction (HER). Critical to HER is the binding of H atoms. While theoretical studies have computed preferred sites and energetics of hydrogen bound to transition metal phosphide surfaces, direct experimental studies are scarce. Herein, we describe measurements of stoichiometry and thermochemistry for hydrogen bound to CoP. We studied both mesoscale CoP particles, exhibiting phosphide surfaces after an acidic pretreatment, and colloidal CoP nanoparticles. Treatment with H2 introduced large amounts of reactive hydrogen to CoP, ca. 0.2 H per CoP unit, and on the order of one H per Co or P surface atom. This was quantified using alkyne hydrogenation and H-atom transfer reactions with phenoxy radicals. Reactive H atoms were even present on the as-prepared materials. On the basis of the reactivity of CoP with various molecular hydrogen donating and accepting reagents, the distribution of binding free energies for H atoms on CoP was estimated to be roughly 51-66 kcal mol-1 (δG°H 0 to -0.7 eV vs H2). Operando X-ray absorption spectroscopy gave preliminary indications about the structure of hydrogenated CoP, showing a slight lattice expansion and no significant change of the effective nuclear charge of Co under H2-flow. These results provide a new picture of catalytically active CoP, with a substantial amount of reactive H atoms. This is likely of fundamental relevance for its catalytic and electrocatalytic properties. Additionally, the approach developed here provides a roadmap to examine hydrogen on other materials.

Triazinyl dyes

-

, (2008/06/13)

Vat dyestuffs of the formula EQU1 wherein R represents alkyl with 1 to 4 carbon atoms, R1 and R2 represent hydrogen or alkyl with 1 to 4 carbon atoms and each of A1 and A2 represents a vattable radical with 3 to 7 condensed rings are characterized by improved resistance to alkali and are suitable for dyeing and printing the most diverse materials, in particular fibers made from natural or regenerated cellulose.

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