Anthrone - ACS, ≥97% , CAS No.90-44-8

CAS: 90-44-8 Cat. No.: A108572 Fórmula: C₁₄H₁₀O Peso molecular: 194.23 Beilstein Registry Number: 1910173 Número CE: 201-994-0

GRAU & PUREZA ACS, ≥97%

Synonyms

9-Oxoanthracene | DTXCID0029391 | DTXSID1049431 | FP0FJ7K744 | A0509 | 9-anthrone | SY010357 | Epitope ID:116188 | Anthracen-9(10H)-one (Anthrone) | SCHEMBL18143 | ANTHRONE | Anthrone, analytical standard | EN300-19192 | AP-065/41069590 | (10H)-9-Anthrace

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Visão geral

Anthrone, also known as 9(10H)-Anthracenone, is a planar tricyclic aromatic ketone. In acidic conditions, anthrone reacts with carbohydrate to yield a blue-green color.
Application
The anthrone method is a colorimetric assay to detect reducing and nonreducing sugars.
Anthrone is used in the quantitative determination of streptomycin.
It has been used to detect carbohydrate containing lipids and to measure sugar content such as sucrose and trehalose in the liquid medium.

Especificações

Sinónimos

9-Oxoanthracene | DTXCID0029391 | DTXSID1049431 | FP0FJ7K744 | A0509 | 9-anthrone | SY010357 | Epitope ID:116188 | Anthracen-9(10H)-one (Anthrone) | SCHEMBL18143 | ANTHRONE | Anthrone, analytical standard | EN300-19192 | AP-065/41069590 | (10H)-9-Anthrace

Especificações e pureza

ACS, ≥97%

Condições de armazenamento de armazenamento

Protected from light,Room temperature,Argon charged

Enviado em

Normal

Grau

ACS

Pureza

≥97%

Nomes e identificadores

Sorrisos canónicos

C1C2=CC=CC=C2C(=O)C3=CC=CC=C31

IUPAC Name

10H-anthracen-9-one

InChIKey

RJGDLRCDCYRQOQ-UHFFFAOYSA-N

INCHI

1S/C14H10O/c15-14-12-7-3-1-5-10(12)9-11-6-2-4-8-13(11)14/h1-8H,9H2

SMILES isoméricas

C1C2=CC=CC=C2C(=O)C3=CC=CC=C31

WGK Alemanha

3

RTECS

CB8925500

Peso molecular

194.23

Beilstein

1910173

Reaxy-Rn

1910173

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1910173&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Anthracenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Anthracenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Anthracenes
• Alternative Parents: Aryl ketones Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Anthracene - Aryl ketone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound
• Descrição: This compound belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings.
• External Descriptors: anthracenes

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

Alvos associados (humanos)

ALOX5 Tclin Arachidonate 5-lipoxygenase (6568 Activities)

Discover Target: ALOX5

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

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

HaCaT (4069 Activities)

Explore this target

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

Alvos associados (não humanos)

Txnrd2 Thioredoxin reductase 2, mitochondrial (18 Activities)

Discover Target: Txnrd2

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

Mecanismos de ação

Propriedades químicas e físicas

• Solubilidade: Soluble in ethyl acetate (20 mg/ml), water (0.5 mg/ml at 20 °C), acetone, ethanol (very slightly), and ether (slightly). Soluble in acetone, hot benzene, concentrated sulfuric acid, hot dilute alkali and most organic solvents. Insoluble in water.
• Sensibilidade: Air sensitive ;Light sensitive
• Ponto de ebulição (°C): 721°C
• Ponto de fusão (°C): 155°C
• Peso molecular: 194.230 g/mol
• XLogP3: 3.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 194.073 Da
• Monoisotopic Mass: 194.073 Da
• Topological Polar Surface Area: 17.100 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 234.000
• 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