2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline

Catalog Number	ACM4733395-4
CAS	4733-39-5
Structure
Synonyms	1,10-Phenanthroline, 2,9-dimethyl-4,7-diphenyl-
IUPAC Name	2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline
Molecular Weight	360.45
Molecular Formula	C26H20N2
Canonical SMILES	CC1=CC(=C2C=CC3=C(C=C(N=C3C2=N1)C)C4=CC=CC=C4)C5=CC=CC=C5
InChI	STTGYIUESPWXOW-UHFFFAOYSA-N
InChI Key	InChI=1S/C26H20N2/c1-17-15-23(19-9-5-3-6-10-19)21-13-14-22-24(20-11-7-4-8-12-20)16-18(2)28-26(22)25(21)27-17/h3-16H,1-2H3
Boiling Point	279 - 283 °C
Melting Point	279-283 °C-lit.
Purity	98%
Density	1.2408 g/ml
Appearance	Yellow powder
EC Number	225-240-5
Exact Mass	360.162648646
Heavy Atom Count	28
Hydrogen Bond Acceptor Count	2
Hydrogen Bond Donor Count	0
Monoisotopic Mass	360.162648646
Rotatable Bond Count	2
Topological Polar Surface Area	25.8 Ų

Q&A

What is the molecular weight of 2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline?

The molecular weight of 2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline is 360.45.

What is the product category of 2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline?

The product categories of 2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline include Industrial/Fine Chemicals, electronic, Electronic Chemicals, Analytical Chemistry, and more.

At what temperature does 2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline melt?

2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline melts at 279-283 °C.

What are the synonyms for 2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline?

Some synonyms for 2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline include Bathocuproine subliMed grade and Bathocuproine.

What is the solubility of 2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline?

2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline is soluble in methanol, ethanol, 2-propanol, benzene, acetone, and partly miscible in water.

What is one of the uses of Bathocuproine?

Bathocuproine is used as a reagent for the determination of copper.

What is the primary function of Bathocuproine in organic photovoltaic cells?

Bathocuproine acts as an exciton-blocking barrier in organic photovoltaic cells, prohibiting exciton diffusion towards the Al electrode.

How is Bathocuproine commonly purified?

Bathocuproine is commonly purified by recrystallization from benzene.

What are some of the safety statements associated with Bathocuproine?

Safety statements associated with Bathocuproine include 24/25-36-26-37/39.

In what type of electronic devices is Bathocuproine commonly used?

Bathocuproine is commonly used in organic electronics and perovskite solar cells as a buffer layer between the acceptor and cathode layers.