1,2,3,4-tetraphenylcyclopenta-1,3-diene

1,2,3,4-tetraphenylcyclopenta-1,3-diene - Names and Identifiers

Name	1,2,3,4-Tetraphenyl-1,3-cyclopentadiene
Synonyms	NSC 72113 1,2,3,4-Tetraphenylcyclopentadiene 1,2,3,4-Tetraphebyl-1,3-cyclopentadene 1,2,3,4-tetraphenylcyclopenta-1,3-diene 1,2,3,4-TETRAPHENYL-1,3-CYCLOPENTADIENE 1,2,3,4-Tetraphenylcyclopenta-1,3-diene 2,3,4,5-Tetraphenyl-2,4-cyclopentadiene 1,2,3,4-Tetraphenyl-1,3-cyclopentadiene 1,3-Cyclopentadiene, 1,2,3,4-tetraphenyl- (8CI) cyclopenta-1,3-diene-1,2,3,4-tetrayltetrabenzene 1,1',1'',1'''-cyclopenta-1,3-diene-1,2,3,4-tetrayltetrabenzene Benzene, 1,1',1'',1'''-(1,3-cyclopentadiene-1,2,3,4-tetrayl)tetrakis- (9CI)
CAS	15570-45-3
EINECS	239-619-8
InChI	InChI=1/C29H22/c1-5-13-22(14-6-1)26-21-27(23-15-7-2-8-16-23)29(25-19-11-4-12-20-25)28(26)24-17-9-3-10-18-24/h1-20H,21H2

1,2,3,4-tetraphenylcyclopenta-1,3-diene - Physico-chemical Properties

Molecular Formula	C29H22
Molar Mass	370.48
Density	1.1223 (estimate)
Melting Point	180-182 °C (lit.)
Boling Point	435.37°C (rough estimate)
Flash Point	280.9°C
Solubility	soluble in Toluene
Vapor Presure	2.83E-11mmHg at 25°C
Appearance	powder to crystal
Color	White to Light yellow to Light orange
Storage Condition	Room Temprature
Refractive Index	1.8780 (estimate)
MDL	MFCD00001355

1,2,3,4-tetraphenylcyclopenta-1,3-diene - Risk and Safety

Safety Description	24/25 - Avoid contact with skin and eyes.
WGK Germany	3
HS Code	29029090

1,2,3,4-tetraphenylcyclopenta-1,3-diene - Introduction

1,2, 3,4-tetraphenyl-1, 3-cyclopentadiene is an organic compound often abbreviated as A (TBCP). The following is an introduction to the nature, use, formulation and safety information of TBCP:

Nature:
- TBCP is a colorless crystal with a low melting point and boiling point.
-It is insoluble in water, but soluble in organic solvents such as benzene and methanol.
- TBCP has stable chemical properties and good heat resistance.

Use:
- TBCP is often used as a starting material for organic synthesis, and can further synthesize a variety of organic compounds, such as high molecular polymers, drugs and dyes.
-It can also be used in the field of electronics, as a component of organic electronic materials, light-emitting diodes and solar cells.

Method:
A common preparation method of-TBCP is through the substitution reaction of cyclopentadiene. Usually, benzene is used as the substitution reagent and the reaction is carried out in the presence of a catalyst.
-The reaction conditions require higher reaction time.

Safety Information:
- TBCP has low toxicity, but it still needs to be handled carefully to avoid inhalation and skin contact.
-When using TBCP, appropriate protective measures should be taken, such as wearing gloves and respiratory protective equipment.
-Laboratory operations involving TBCP should be carried out in a well-ventilated place to avoid the accumulation of harmful substances.

Last Update：2024-04-09 02:00:42