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CAS No.: | 21890-57-3 |
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Name: | 3-chloro-5-hydroxy-2-methylnaphthalene-1,4-dione |
Molecular Structure: | |
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Formula: | C11H7ClO3 |
Molecular Weight: | 222.628 |
Synonyms: | CHLOROPLUMBAGIN;5-hydroxy-2-methyl-3-chloro-1,4-naphthoquinone;2-methyl-3-chloro-5-hydroxy-1,4-naphthoquinone;3-Chloro-plumbagin; |
Density: | 1.49g/cm3 |
Boiling Point: | 389.3°C at 760 mmHg |
Flash Point: | 189.3°C |
PSA: | 54.37000 |
LogP: | 2.28400 |
5-hydroxy-2-methyl-1,4-naphthoquinone
A
5-hydroxy-2-methyl-3-chloro-1,4-naphthoquinone
B
3,6-dichloro-5-hydroxy-2-methyl-[1,4]naphthoquinone
Conditions | Yield |
---|---|
With chlorine; acetic acid |
5-hydroxy-2-methyl-1,4-naphthoquinone
5-hydroxy-2-methyl-3-chloro-1,4-naphthoquinone
Conditions | Yield |
---|---|
With chlorine In chloroform for 24h; Ambient temperature; | 85 mg |
With hydrogenchloride; potassium permanganate; acetic acid; sodium acetate for 1h; | 240 mg |
3-Chlorplumbaginacetat
5-hydroxy-2-methyl-3-chloro-1,4-naphthoquinone
Conditions | Yield |
---|---|
With aluminium trichloride In dichloromethane for 3h; Ambient temperature; |
3-chlorojuglone
dimethyl sulfoxide
5-hydroxy-2-methyl-3-chloro-1,4-naphthoquinone
Conditions | Yield |
---|---|
With dihydrogen peroxide 1.) dioxan, room temp., 30 min, 2.) dioxan, 15 min; Yield given. Multistep reaction; |
5-Acetoxy-3-chlor-1,4-naphthochinon
dimethyl sulfoxide
5-hydroxy-2-methyl-3-chloro-1,4-naphthoquinone
Conditions | Yield |
---|---|
Yield given. Multistep reaction; |
5-Acetoxy-3-chlor-1,4-naphthochinon
A
5-hydroxy-2-methyl-3-chloro-1,4-naphthoquinone
Conditions | Yield |
---|---|
With ammonium peroxydisulfate; aluminium trichloride; silver nitrate; 4-nitro-benzoic acid 1.) CH3CN, water, 80 deg C, 40 min, 2.) CH2Cl2, r.t., 3 h; Yield given. Multistep reaction. Yields of byproduct given; |
5-Acetoxy-3-chlor-1,4-naphthochinon
4-nitro-benzoic acid
A
5-hydroxy-2-methyl-3-chloro-1,4-naphthoquinone
B
nitrobenzene
Conditions | Yield |
---|---|
With ammonium peroxydisulfate; aluminium trichloride; silver nitrate 1.) CH3CN, water, 80 deg C, 40 min, 2.) CH2Cl2, r.t., 3 h; Yield given. Multistep reaction. Yields of byproduct given; |
5-hydroxy-2-methyl-1,4-naphthoquinone
A
5-hydroxy-2-methyl-3-chloro-1,4-naphthoquinone
B
2-methyl-5-hydroxy-2,3-epoxy-2,3-dihydro-1,4-naphthoquinone
Conditions | Yield |
---|---|
With hydrogenchloride; sodium perborate; sulfuric acid 1.) ethanol, 2 min; Yield given. Multistep reaction. Yields of byproduct given; |
acetic acid
5-hydroxy-2-methyl-3-chloro-1,4-naphthoquinone
Conditions | Yield |
---|---|
With diacetyl peroxide |
5-hydroxy-2-methyl-1,4-naphthoquinone
A
5-hydroxy-2-methyl-3-chloro-1,4-naphthoquinone
Conditions | Yield |
---|---|
With chlorine; acetic acid |