1,2-Diaminoanthraquinone - ≥90%, used for 1,2-Diaminoanthraquinone (DAQ) can be used as a building block to prepare: Imidazoanthraquinone derivatives via palladium-catalyzed Suzuki–Miyaura and Sonogashira coupling reactions. Anthra[1,2-d]imidazole-6,11-di

CAS: 1758-68-5 Cat. No.: D124352 Summenformel: C₁₄H₁₀N₂O₂ Molekulargewicht: 238.24 EG-Nummer: 217-156-2

QUALITÄT & REINHEIT ≥90%

Synonyms

1,2-diamino-10-anthracenedione | NSC 39934 | BDBM50599586 | BIDD:GT0412 | MFCD00001219 | CCRIS 5602 | 1, 2-Diaminoanthraquinone | UPCMLD0ENAT5883742:001 | ANTHRAQUINONE, 1,2-DIAMINO- | EINECS 217-156-2 | SCHEMBL487001 | 1,2-Diamino-9,10-anthraquinone | 1,

Storage

Room temperature,Argon charged,Desiccated

Shipped In

Normal

Übersicht

1,2-Diaminoanthraquinone is a useful reagent for the direct detection of nitric oxide (NO) DAA is non-fluorescent; however, it reacts with NO, in the presence of oxygen, to form DAA triazole, yielding red fluorescence, which is visible with a rhodamine filter (λ ≥ 580 nm).
For the direct detection of nitric oxide.

Spezifikationen

Synonyme

1,2-diamino-10-anthracenedione | NSC 39934 | BDBM50599586 | BIDD:GT0412 | MFCD00001219 | CCRIS 5602 | 1, 2-Diaminoanthraquinone | UPCMLD0ENAT5883742:001 | ANTHRAQUINONE, 1,2-DIAMINO- | EINECS 217-156-2 | SCHEMBL487001 | 1,2-Diamino-9,10-anthraquinone | 1,

Spezifikationen & Reinheit

≥90%

Anmeldung

1,2-Diaminoanthraquinone (DAQ) can be used as a building block to prepare: Imidazoanthraquinone derivatives via palladium-catalyzed Suzuki–Miyaura and Sonogashira coupling reactions. Anthra[1,2-d]imidazole-6,11-diones by reacting with various aldehydes in

Storage

Room temperature,Argon charged,Desiccated

Verschickt in

Normal

Reinheit

≥90%

Namen und Kennungen

Pubchem Sid

504752689

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504752689

Kanonisches Lächeln

C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3)N)N

IUPAC Name

1,2-diaminoanthracene-9,10-dione

InChIKey

LRMDXTVKVHKWEK-UHFFFAOYSA-N

INCHI

1S/C14H10N2O2/c15-10-6-5-9-11(12(10)16)14(18)8-4-2-1-3-7(8)13(9)17/h1-6H,15-16H2

Isomere SMILES

C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3)N)N

WGK Deutschland

3

RTECS

CB6200000

Molekulargewicht

238.24

Reaxy-Rn

2125604

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2125604&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Klasse Anthracenes
      • Subclass Anthraquinones

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: Anthracenes
• Subclass: Anthraquinones
• Intermediate Tree Nodes: Not available
• Direct Parent: 2-aminoanthraquinones
• Alternative Parents: Aryl ketones Vinylogous amides Primary amines Organopnictogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: 2-aminoanthraquinone - Aryl ketone - Vinylogous amide - Ketone - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Aromatic homopolycyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as 2-aminoanthraquinones. These are organic compounds containing an anthraquinone ring system, which is substituted at the 2-position by an amino group.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Zugehörige Ziele (menschlich)

MAOA Tclin Monoamine oxidase A (11911 Activities)

Discover Target: MAOA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MAOB Tclin Monoamine oxidase B (8835 Activities)

Discover Target: MAOB

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TERT Tchem Telomerase reverse transcriptase (2428 Activities)

Discover Target: TERT

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: Soluble in DMSO (5 mg/ml). Insoluble in water.
• Empfindlichkeit: Air sensitive
• Schmelzpunkt (°C): 289-291°C
• Molekulargewicht: 238.240 g/mol
• XLogP3: 2.100
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 238.074 Da
• Monoisotopic Mass: 238.074 Da
• Topological Polar Surface Area: 86.200 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 382.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1