Cas no 86533-36-0 (Aristolindiquinone)

Aristolindiquinone structure
Aristolindiquinone structure
Product Name:Aristolindiquinone
CAS No:86533-36-0
MF:C12H10O4
MW:218.205403804779
CID:1852493
PubChem ID:442723
Update Time:2024-10-26

Aristolindiquinone Chemical and Physical Properties

Names and Identifiers

    • 4,5-dihydroxy-3,8-dimethylnaphthalene-1,2-dione
    • Aristolindiquinone
    • C10300
    • 2,5-Dihydroxy-3,8-dimethyl-1,4-naphthalenedione
    • 2,5-dihydroxy-3,8-dimethyl-1,4-naphthoquinone
    • Q27105837
    • 2,5-Dihydroxy-3,8-dimethyl-1,4-naphthalenedione (ACI)
    • DTXSID80331925
    • HY-N2471
    • AKOS040760276
    • CS-0022741
    • 86533-36-0
    • CHEBI:2823
    • AC1L9DAN
    • DTXCID60283019
    • DA-61206
    • Inchi： 1S/C12H10O4/c1-5-3-4-7(13)9-8(5)12(16)11(15)6(2)10(9)14/h3-4,13,15H,1-2H3
    • InChI Key： BEBGSFZOQXPJCT-UHFFFAOYSA-N
    • SMILES： O=C1C2C(=C(C=CC=2C)O)C(=O)C(C)=C1O

Computed Properties

  • Exact Mass: 218.05790880 g/mol
  • Monoisotopic Mass: 218.05790880 g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 0
  • Complexity: 383
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Molecular Weight: 218.20
  • XLogP3: 1.8
  • Topological Polar Surface Area: 74.6

Experimental Properties

  • Color/Form: Powder
  • Density: 1.452±0.06 g/cm3 (20 oC 760 Torr),
  • Solubility: Almost insoluble (0.028 g/l) (25 o C),

Aristolindiquinone Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI TAO SHU Biotechnology Co., Ltd.
TN1400-1 mg
Aristolindiquinone
 86533-36-0
1mg
 ￥4833.00 2022-04-26
TargetMol Chemicals
TN1400-5mg
Aristolindiquinone
 86533-36-0
5mg
 ￥ 3800 2024-07-20
TargetMol Chemicals
TN1400-5 mg
Aristolindiquinone
 86533-36-0 98%
5mg
 ￥ 3,800 2023-07-11
SHANG HAI TAO SHU Biotechnology Co., Ltd.
TN1400-1 mL * 10 mM (in DMSO)
Aristolindiquinone
 86533-36-0
1 mL * 10 mM (in DMSO)
 ￥ 3900 2023-09-07
TargetMol Chemicals
TN1400-1 ml * 10 mm
Aristolindiquinone
 86533-36-0
1 ml * 10 mm
 ￥ 3900 2024-07-20

Aristolindiquinone Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Monopotassium phosphate ,  Potassium nitrosodisulfonate Solvents: Methanol ,  Water
2.1 Reagents: Sulfuric acid Solvents: Methanol ,  Acetic anhydride
2.2 Reagents: Sodium methoxide Solvents: Methanol
3.1 Reagents: Hydrogen bromide Solvents: Water
Reference
Studies on Indian medicinal plants. Part LXXIX. Synthesis proves the structure of aristolindiquinone
Achari, Basudeb; et al, Tetrahedron, 1985, 41(1), 107-10

Production Method 2

Reaction Conditions
1.1 Reagents: Sodium dichromate Solvents: Dimethyl sulfoxide
1.2 Reagents: Sulfuric acid
2.1 Reagents: Zinc ,  Iodine Solvents: Diethyl ether ,  Benzene
3.1 Reagents: Potassium hydroxide Solvents: Methanol
4.1 Reagents: Oxalyl chloride Solvents: Benzene
4.2 Reagents: Tin tetrachloride Solvents: Benzene
4.3 Reagents: Hydrochloric acid Solvents: Water
5.1 Reagents: Monopotassium phosphate ,  Potassium nitrosodisulfonate Solvents: Methanol ,  Water
6.1 Reagents: Sulfuric acid Solvents: Methanol ,  Acetic anhydride
6.2 Reagents: Sodium methoxide Solvents: Methanol
7.1 Reagents: Hydrogen bromide Solvents: Water
Reference
Studies on Indian medicinal plants. Part LXXIX. Synthesis proves the structure of aristolindiquinone
Achari, Basudeb; et al, Tetrahedron, 1985, 41(1), 107-10

Production Method 3

Reaction Conditions
1.1 Reagents: Hydrogen bromide Solvents: Water
Reference
Studies on Indian medicinal plants. Part LXXIX. Synthesis proves the structure of aristolindiquinone
Achari, Basudeb; et al, Tetrahedron, 1985, 41(1), 107-10

Production Method 4

Reaction Conditions
1.1 Reagents: Sulfuric acid Solvents: Methanol ,  Acetic anhydride
1.2 Reagents: Sodium methoxide Solvents: Methanol
2.1 Reagents: Hydrogen bromide Solvents: Water
Reference
Studies on Indian medicinal plants. Part LXXIX. Synthesis proves the structure of aristolindiquinone
Achari, Basudeb; et al, Tetrahedron, 1985, 41(1), 107-10

Production Method 5

Reaction Conditions
1.1 Reagents: Oxalyl chloride Solvents: Benzene
1.2 Reagents: Tin tetrachloride Solvents: Benzene
1.3 Reagents: Hydrochloric acid Solvents: Water
2.1 Reagents: Monopotassium phosphate ,  Potassium nitrosodisulfonate Solvents: Methanol ,  Water
3.1 Reagents: Sulfuric acid Solvents: Methanol ,  Acetic anhydride
3.2 Reagents: Sodium methoxide Solvents: Methanol
4.1 Reagents: Hydrogen bromide Solvents: Water
Reference
Studies on Indian medicinal plants. Part LXXIX. Synthesis proves the structure of aristolindiquinone
Achari, Basudeb; et al, Tetrahedron, 1985, 41(1), 107-10

Production Method 6

Reaction Conditions
1.1 Reagents: Potassium hydroxide Solvents: Methanol
2.1 Reagents: Oxalyl chloride Solvents: Benzene
2.2 Reagents: Tin tetrachloride Solvents: Benzene
2.3 Reagents: Hydrochloric acid Solvents: Water
3.1 Reagents: Monopotassium phosphate ,  Potassium nitrosodisulfonate Solvents: Methanol ,  Water
4.1 Reagents: Sulfuric acid Solvents: Methanol ,  Acetic anhydride
4.2 Reagents: Sodium methoxide Solvents: Methanol
5.1 Reagents: Hydrogen bromide Solvents: Water
Reference
Studies on Indian medicinal plants. Part LXXIX. Synthesis proves the structure of aristolindiquinone
Achari, Basudeb; et al, Tetrahedron, 1985, 41(1), 107-10

Production Method 7

Reaction Conditions
1.1 Reagents: Zinc ,  Iodine Solvents: Diethyl ether ,  Benzene
2.1 Reagents: Potassium hydroxide Solvents: Methanol
3.1 Reagents: Oxalyl chloride Solvents: Benzene
3.2 Reagents: Tin tetrachloride Solvents: Benzene
3.3 Reagents: Hydrochloric acid Solvents: Water
4.1 Reagents: Monopotassium phosphate ,  Potassium nitrosodisulfonate Solvents: Methanol ,  Water
5.1 Reagents: Sulfuric acid Solvents: Methanol ,  Acetic anhydride
5.2 Reagents: Sodium methoxide Solvents: Methanol
6.1 Reagents: Hydrogen bromide Solvents: Water
Reference
Studies on Indian medicinal plants. Part LXXIX. Synthesis proves the structure of aristolindiquinone
Achari, Basudeb; et al, Tetrahedron, 1985, 41(1), 107-10

Production Method 8

Reaction Conditions
1.1 Reagents: Trifluoroacetic acid
2.1 Reagents: Sodium dichromate Solvents: Dimethyl sulfoxide
2.2 Reagents: Sulfuric acid
3.1 Reagents: Zinc ,  Iodine Solvents: Diethyl ether ,  Benzene
4.1 Reagents: Potassium hydroxide Solvents: Methanol
5.1 Reagents: Oxalyl chloride Solvents: Benzene
5.2 Reagents: Tin tetrachloride Solvents: Benzene
5.3 Reagents: Hydrochloric acid Solvents: Water
6.1 Reagents: Monopotassium phosphate ,  Potassium nitrosodisulfonate Solvents: Methanol ,  Water
7.1 Reagents: Sulfuric acid Solvents: Methanol ,  Acetic anhydride
7.2 Reagents: Sodium methoxide Solvents: Methanol
8.1 Reagents: Hydrogen bromide Solvents: Water
Reference
Studies on Indian medicinal plants. Part LXXIX. Synthesis proves the structure of aristolindiquinone
Achari, Basudeb; et al, Tetrahedron, 1985, 41(1), 107-10

Production Method 9

Reaction Conditions
1.1 Reagents: Sodium hydroxide Solvents: Water
2.1 Reagents: Trifluoroacetic acid
3.1 Reagents: Sodium dichromate Solvents: Dimethyl sulfoxide
3.2 Reagents: Sulfuric acid
4.1 Reagents: Zinc ,  Iodine Solvents: Diethyl ether ,  Benzene
5.1 Reagents: Potassium hydroxide Solvents: Methanol
6.1 Reagents: Oxalyl chloride Solvents: Benzene
6.2 Reagents: Tin tetrachloride Solvents: Benzene
6.3 Reagents: Hydrochloric acid Solvents: Water
7.1 Reagents: Monopotassium phosphate ,  Potassium nitrosodisulfonate Solvents: Methanol ,  Water
8.1 Reagents: Sulfuric acid Solvents: Methanol ,  Acetic anhydride
8.2 Reagents: Sodium methoxide Solvents: Methanol
9.1 Reagents: Hydrogen bromide Solvents: Water
Reference
Studies on Indian medicinal plants. Part LXXIX. Synthesis proves the structure of aristolindiquinone
Achari, Basudeb; et al, Tetrahedron, 1985, 41(1), 107-10

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