9,10-Di(2-naphthyl)anthracene

Suppliers

Names

[ CAS No. ]:
122648-99-1

[ Name ]:
9,10-Di(2-naphthyl)anthracene

[Synonym ]:
9,10-Di(naphthalen-2-yl)anthracen
9,10-Di(naphthalen-2-yl)anthracene
9,10-dinaphthalen-2-ylanthracene
Anthracene, 9,10-di-2-naphthalenyl-
9,10-Di-2-naphthalenyl-anthracene,ADN
MFCD00028944
9,10-Di(2-naphthyl)anthracene
9,10-Di(naphth-2-yl)anthracene

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
595.4±45.0 °C at 760 mmHg

[ Melting Point ]:
382-384ºC

[ Molecular Formula ]:
C34H22

[ Molecular Weight ]:
430.539

[ Flash Point ]:
314.8±22.8 °C

[ Exact Mass ]:
430.172150

[ LogP ]:
10.66

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.761

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
36/37/38

[ RIDADR ]:
NONH for all modes of transport

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 2-Bromonaphthalene
  • 9,10-Dibromo anthracene
  • 9,10-di-[2]naphthyl-9,10-dihydro-anthracene-9,10-diol
  • Anthraquinone

DownStream

Articles

Biosynthesis of cell envelope-associated phenolic glycolipids in Mycobacterium marinum.

J. Bacteriol. 197(6) , 1040-50, (2015)

Phenolic glycolipids (PGLs) are polyketide synthase-derived glycolipids unique to pathogenic mycobacteria. PGLs are found in several clinically relevant species, including various Mycobacterium tuberc...

Adenosine conjugated lipidic nanoparticles for enhanced tumor targeting.

Int. J. Pharm. 486 , 287-96, (2015)

Delivering chemotherapeutics by nanoparticles into tumor is impeded majorly by two factors: nonspecific targeting and inefficient penetration. Targeted delivery of anti-cancer agents solely to tumor c...

Genetic and chemical validation identifies Mycobacterium tuberculosis topoisomerase I as an attractive anti-tubercular target.

Tuberculosis (Edinb.) 95 , 589-98, (2015)

DNA topoisomerases perform the essential function of maintaining DNA topology in prokaryotes. DNA gyrase, an essential enzyme that introduces negative supercoils, is a clinically validated target. How...


More Articles

Related Compounds

  • 9,10-Di(2-naphthyl)anthracene
  • 2-Bromo-9,10-di(2-naphthyl)anthracene
  • 2-Methyl-9,10-di(2-naphthyl)anthracene
  • 2,6-Dibromo-9,10-di(2-naphthyl)anthracene
  • 9,10-di(2-naphthyl)anthracene-2-boronic acid
  • 2-(2-Methyl-2-propanyl)-9,10-di(2-naphthyl)anthracene
  • Benzenemethanamine, 3-chloro-I+/--(1-ethylpentyl)-N-methyl-
  • 4-Amino-4-cyclopropylpent-1-en-3-one
  • (3-Chlorophenyl)[4-(trifluoromethoxy)phenyl]methanamine
  • 1,1,1-Trifluoro-3-(1,2,3,4-tetrahydronaphthalen-1-yl)propan-2-amine
  • 1H-1,2,4-Triazole-5-ethanol, I+/--(4,5-dibromo-2-thienyl)-1-methyl-
  • 4-(2-Methylpiperidin-3-yl)-1lambda6-thiomorpholine-1,1-dione
  • 1-{5-[(Propan-2-yloxy)methyl]-1,3,4-thiadiazol-2-yl}ethan-1-amine
  • 2-[(Tert-butoxy)methyl]-4-methyl-1,3-oxazole-5-carboxylic acid
  • 1-(6-Chloro-2-pyrazinyl)-3-azetidinamine
  • 3-Chloro-2-propoxy-benzylamine
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.