D206008
trans,trans-1,4-Diphenyl-1,3-butadiene
98%
Synonym(s):
β,β′-Bistyryl, DPB
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25 G
R 2 254,98
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25 G
R 2 254,98
About This Item
Linear Formula:
C6H5CH=CHCH=CHC6H5
CAS Number:
Molecular Weight:
206.28
Beilstein:
1905939
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
form:
crystals
Assay:
98%
Recommended Products
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
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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.[3]
- 2,5-diphenylthiophene by oxidation reaction with potassium sulfide and DMSO.[1]
- 2-[(3E)-4-Phenyl-2-(phenylmethyl)-3-buten-1-yl]furan via nickel catalyzed hydrobenzylation reaction with furfural in the presence of N2H4.[2]
It can also be used as a ligand to prepare silver(I) coordination polymers by reacting with silver(I) salts.[3]
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Nickel-catalyzed regioselective hydrobenzylation of 1, 3-dienes with hydrazones
Lv Leiyang, et al.
ACS Catalysis, 9(10), 9199-9205 (2019)
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
David P Burgner et al.
PloS one, 10(5), e0125342-e0125342 (2015-05-06)
Pathogen-specific and overall infection burden may contribute to atherosclerosis and cardiovascular disease (CVD), but the effect of infection severity and timing is unknown. We investigated whether childhood infection-related hospitalisation (IRH, a marker of severity) was associated with subsequent adult CVD
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)
Mustafa Toprakçí et al.
Bioorganic & medicinal chemistry letters, 15(20), 4438-4446 (2005-09-03)
Monoamine oxidase (EC1.4.3.4; MAO) is a mitochondrial outer membrane flavoenzyme that catalyzes the oxidation of biogenic amines. It has two distinct isozymic forms designated MAO-A and MAO-B, each displaying different substrate and inhibitor specificities. They are the well-known targets for
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