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Technology Process of 4-Amino-1-bromo-9,10-dihydro-9,10-dioxoanthracene-3,5-disulphonic acid

4-Amino-1-bromo-9,10-dihydro-9,10-dioxoanthracene-3,5-disulphonic acid

Base Information
  • Chemical Name:4-Amino-1-bromo-9,10-dihydro-9,10-dioxoanthracene-3,5-disulphonic acid
  • CAS No.:82-32-6
  • Molecular Formula:C14H8 Br N O8 S2
  • Molecular Weight:462.24922
  • Hs Code.:
  • European Community (EC) Number:201-410-4
  • DSSTox Substance ID:DTXSID30231507
  • Nikkaji Number:J192.600D
  • Wikidata:Q83112448
  • Mol file:82-32-6.mol
4-Amino-1-bromo-9,10-dihydro-9,10-dioxoanthracene-3,5-disulphonic acid

Synonyms:82-32-6;4-Amino-1-bromo-9,10-dihydro-9,10-dioxoanthracene-3,5-disulphonic acid;8-amino-5-bromo-9,10-dioxoanthracene-1,7-disulfonic acid;EINECS 201-410-4;C14H8BrNO8S2;DTXSID30231507;1,7-Anthracenedisulfonic acid, 8-amino-5-bromo-9,10-dihydro-9,10-dioxo-;8-Amino-5-bromo-9,10-dihydro-9,10-dioxo-1,7-anthracenedisulfonic acid

Suppliers and Price of 4-Amino-1-bromo-9,10-dihydro-9,10-dioxoanthracene-3,5-disulphonic acid
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 4-Amino-1-bromo-9,10-dihydro-9,10-dioxoanthracene-3,5-disulphonic acid
Chemical Property:
  • PSA：185.66000 
  • Density:2.072g/cm3 
  • LogP:4.04290 
  • XLogP3:0.9
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:9
  • Rotatable Bond Count:2
  • Exact Mass:460.88747
  • Heavy Atom Count:26
  • Complexity:830
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC2=C(C(=C1)S(=O)(=O)O)C(=O)C3=C(C(=CC(=C3C2=O)Br)S(=O)(=O)O)N
Refernces

Expedient synthesis of a novel class of pseudoaromatic amino acids: Tetrahydroindazol-3-yl- and tetrahydrobenzisoxazol-3-ylalanine derivatives

10.1016/j.tetlet.2003.11.133

The study presents a concise synthesis method for a novel class of homochiral aromatic amino acid surrogates, featuring tetrahydroindazole or benzisoxazole systems. These surrogates were synthesized through the acylation of cyclic 1,3-diketone by the side-chain carboxyl functionality of specific amino acid precursors, followed by a regioselective condensation with hydrazine, N-benzylhydrazine, and hydroxylamine. The synthetic strategy is versatile, allowing for the creation of structurally diverse derivatives. These novel amino acids can be efficiently incorporated into proteins and have potential applications in imparting unique properties to biological peptides. The study also includes the synthesis of Na-Fmoc-protected derivatives, which are useful for solid-phase peptide assembly, and the exploration of the stereochemistry integrity of the homochiral starting material through chemical transformations. The synthesized amino acids offer opportunities as structural surrogates of tryptophan and as building blocks for designing molecular probes.

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