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16,17-dimethoxyanthra[9,1,2-cde]benzo[rst]pentaphene-5,10-diyl bis(hydrogen sulphate)

  • CAS:2678-71-9
  • purity:99%
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Details

Buy Good Quality 16,17-dimethoxyanthra[9,1,2-cde]benzo[rst]pentaphene-5,10-diyl bis(hydrogen sulphate) 2678-71-9 with a minimum purity of 99%

  • Molecular Formula: C36H22 O10 S2
  • Molecular Weight: 678.697
  • Boiling Point: °Cat760mmHg 
  • Flash Point: °C 
  • PSA: 162.42000 
  • Density: 1.684g/cm3 
  • LogP: 10.32980 

16,17-dimethoxyanthra[9,1,2-cde]benzo[rst]pentaphene-5,10-diyl bis(hydrogen sulphate)(Cas 2678-71-9) Usage

Type of compound

Complex chemical compound
16,17-dimethoxyanthra[9,1,2-cde]benzo[rst]pentaphene-5,10-diyl bis(hydrogen sulphate) has a long and complicated name, indicating its complex nature.

Bis(hydrogen sulphate) salt

Contains two sulfate groups
The presence of two sulfate groups suggests potential applications in various chemical processes.

Fused polycyclic aromatic hydrocarbon

Contains dimethoxyanthra[9,1,2-cde]benzo[rst]pentaphene-5,10-diyl
The compound's molecular structure features a fused polycyclic aromatic hydrocarbon, which may contribute to its potential industrial and research applications.

Potential applications

Industrial and/or research applications
Given its complex molecular structure and the presence of sulfate groups, this chemical may have a range of potential uses in various fields.

Complex chemical properties

Likely to have complex and varied chemical properties
The complexity of the compound's structure and name suggests that it may exhibit a wide range of chemical properties.

Molecular structure

Contains multiple fused rings and functional groups

Solubility

Unknown, but potentially soluble in organic solvents
Given the presence of aromatic hydrocarbons and other functional groups, the compound may be soluble in organic solvents such as chloroform or acetone. However, this property would need to be confirmed through experimental testing.

Stability

Unknown, but may be sensitive to heat, light, or moisture
The stability of the compound is not provided, but it may be sensitive to heat, light, or moisture due to the presence of sulfate groups and aromatic hydrocarbons.

Reactivity

Unknown, but may react with nucleophiles, electrophiles, or other reactive species
The reactivity of the compound is not provided, but it may be reactive towards nucleophiles, electrophiles, or other reactive species due to the presence of its complex molecular structure and functional groups.

General Description

"16,17-dimethoxyanthra[9,1,2-cde]benzo[rst]pentaphene-5,10-diyl bis(hydrogen sulphate)" is a complex chemical compound with a long and complicated name. It is a type of bis(hydrogen sulphate) salt with the molecular structure containing two sulfate groups. The compound also contains dimethoxyanthra[9,1,2-cde]benzo[rst]pentaphene-5,10-diyl, which is a fused polycyclic aromatic hydrocarbon. This chemical is likely to have a range of potential industrial and/or research applications given its complex molecular structure and the presence of sulfate groups, which have demonstrated utility in a variety of chemical processes. Given the complexity of the compound's structure and name, it likely has complex and varied chemical properties.

InChI:InChI=1/C36H22O10S2/c1-43-27-15-25-17-7-3-5-9-21(17)35(45-47(37,38)39)23-13-11-19-20-12-14-24-30-26(18-8-4-6-10-22(18)36(24)46-48(40,41)42)16-28(44-2)34(32(20)30)33(27)31(19)29(23)25/h3-16H,1-2H3,(H,37,38,39)(H,40,41,42)

2678-71-9 Process route

Jade Green XBN
128-58-5

Jade Green XBN

16,17-dimethoxy-5,10-bis-sulfooxy-anthra[9,1,2-<i>cde</i>]benzo[<i>rst</i>]pentaphene
2678-71-9

16,17-dimethoxy-5,10-bis-sulfooxy-anthra[9,1,2-cde ]benzo[rst ]pentaphene

Conditions
Conditions Yield
With pyridine; chlorosulphuric acid; hydrogen sulfide; at 50 ℃;
With pyridine; sodium sulfide; anschliessendes Behandeln mit Chloroschwefelsaeure, zuletzt bei 45grad;
With sodium hydroxide; sodium dithionite; anschliessendes Behandeln mit Sulfo-trimethyl-ammonium-betain;
With sodium hydroxide; sodium dithionite; at 50 ℃; Behandeln des Reaktionsprodukts mit Chloroschwefelsaeure-methylester, Pyridin und Zink-Pulver, zuletzt bei 60grad;
With pyridine; sodium sulfide; anschliessendes Behandeln mit Chloroschwefelsaeure, zuletzt bei 45grad;
With pyridine; chlorosulphuric acid; hydrogen sulfide; at 50 ℃;
16,17-dimethoxy-anthra[9,1,2-<i>cde</i>]benzo[<i>rst</i>]pentaphene-5,10-diol
3951-01-7

16,17-dimethoxy-anthra[9,1,2-cde ]benzo[rst ]pentaphene-5,10-diol

16,17-dimethoxy-5,10-bis-sulfooxy-anthra[9,1,2-<i>cde</i>]benzo[<i>rst</i>]pentaphene
2678-71-9

16,17-dimethoxy-5,10-bis-sulfooxy-anthra[9,1,2-cde ]benzo[rst ]pentaphene

Conditions
Conditions Yield
With pyridine; chlorosulphuric acid;
With pyridine; chlorosulphuric acid; toluene;

2678-71-9 Upstream products

  • 42824-16-8
    42824-16-8

    pyridine-SO3 complex

  • 3951-01-7
    3951-01-7

    16,17-dimethoxy-anthra[9,1,2-cde ]benzo[rst ]pentaphene-5,10-diol

  • 128-58-5
    128-58-5

    Jade Green XBN