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TRANS,TRANS-1,4-DIPHENYL-1,3-BUTADIENE

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TRANS,TRANS-1,4-DIPHENYL-1,3-BUTADIENE Basic information

Product Name:
TRANS,TRANS-1,4-DIPHENYL-1,3-BUTADIENE
Synonyms:
  • 1,4-DIPHENYL-1,3-BUTADIENE
  • TRANS,TRANS-1,4-DIPHENYL-1,3-BUTADIENE
  • TRANS,TRANS-1,4-DIPHENYLBUTA-1,3-DIENE
  • T,T-1,4-DIPHENYL-1,3-BUTADIENE
  • (1E,3E)-1,4-Diphenylbuta-1,3-diene
  • (E,E)-(C6H5CH=CH)2
  • E,E)-1,4-Diphenylbutadiene
  • ll-trans-diphenylbutadiene
CAS:
538-81-8
MF:
C16H14
MW:
206.28
EINECS:
629-554-7
Product Categories:
  • Acyclic
  • Alkenes
  • Analytical Reagents
  • Analytical/Chromatography
  • Biochemicals and Reagents
  • Building Blocks
  • Chemical Synthesis
  • Fluorescence/Luminescence Spectroscopy
  • Luminescent Compounds/Detection
  • Organic Building Blocks
  • Scintillation Reagents
  • Spectroscopy
Mol File:
538-81-8.mol
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TRANS,TRANS-1,4-DIPHENYL-1,3-BUTADIENE Chemical Properties

Melting point:
150-152 °C(lit.)
Boiling point:
350 °C(lit.)
Density 
1.151 g/cm3
refractive index 
1.5000 (estimate)
Flash point:
350°C/720mm
storage temp. 
Sealed in dry,Room Temperature
form 
Crystals or Crystalline Powder
color 
White to slightly yellow
Water Solubility 
Slightly soluble in water.
Merck 
14,3320
BRN 
1905937
Stability:
Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey
JFLKFZNIIQFQBS-FNCQTZNRSA-N
CAS DataBase Reference
538-81-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
10-23
TSCA 
Yes
HS Code 
29029000

MSDS

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TRANS,TRANS-1,4-DIPHENYL-1,3-BUTADIENE Usage And Synthesis

Chemical Properties

light yellow crystalline powder

Uses

trans,trans-1,4-Diphenyl-1,3-butadiene reacts with Rieke metal complexes of barium and strontium to prepare metal-diene reagents, which is used for the carbocyclization with dichloroalkanes.

Definition

ChEBI: 1,4-diphenylbutadiene is an alkadiene. It has a role as a fluorochrome.

Purification Methods

Its solution in pet ether (b 60-70o) is chromatographed on an alumina-Celite column (4:1), and the column is washed with the same solvent. The main zone is cut out, eluted with ethanol and transferred to pet ether, which is then dried and evaporated [Pinckard et al. J Am Chem Soc 70 1938 1948]. Recrystallise it from hexane. [Beilstein 5 H 676, 9 IV 2319.]

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