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About This Item
Linear Formula:
C6H5CH=CHCH=CHC6H5
CAS Number:
Molecular Weight:
206.28
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1905939
Assay:
98%
Form:
crystals
Quality Level
assay
98%
form
crystals
bp
350 °C (lit.)
mp
150-152 °C (lit.)
SMILES string
c1ccc(cc1)\C=C\C=C\c2ccccc2
InChI
1S/C16H14/c1-3-9-15(10-4-1)13-7-8-14-16-11-5-2-6-12-16/h1-14H/b13-7+,14-8+
InChI key
JFLKFZNIIQFQBS-FNCQTZNRSA-N
Application
trans,trans-1,4-Diphenyl-1,3-butadiene can be used as a reactant to synthesize:
It can also be used as a ligand to prepare silver(I) coordination polymers by reacting with silver(I) salts.
- 2,5-diphenylthiophene by oxidation reaction with potassium sulfide and DMSO.
- 2-[(3E)-4-Phenyl-2-(phenylmethyl)-3-buten-1-yl]furan via nickel catalyzed hydrobenzylation reaction with furfural in the presence of N2H4.
It can also be used as a ligand to prepare silver(I) coordination polymers by reacting with silver(I) salts.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Liang Chen et al.
Organic letters, 20(23), 7392-7395 (2018-11-22)
A novel, atom economical, and transition-metal-free strategy for the synthesis of thiophenes from substituted buta-1-enes with potassium sulfide has been presented. The reaction achieves double C-S bond formations via cleavage of multiple C-H bonds and provides an efficient approach to
Nickel-catalyzed regioselective hydrobenzylation of 1, 3-dienes with hydrazones
Lv Leiyang, et al.
ACS Catalysis, 9(10), 9199-9205 (2019)
Syntheses and structural studies on silver (I) coordination polymers with trans, trans-1, 4-dipenyl-1, 3-butadiene
Zhong JC, et al.
Inorganica chimica acta, 342, 202-208 (2003)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| D206008-5G | 04061833317488 |
| D206008-25G | 04061833561485 |
