ChemicalBook--->CAS DataBase List--->58743-78-5

58743-78-5

58743-78-5 Structure

58743-78-5 Structure
IdentificationMore
[Name]

4-Ethoxy-[1,1'-biphenyl]-4'-carbonitrile
[CAS]

58743-78-5
[Synonyms]

2OCB
4-(4'-N-ETHYLOXYBIPHENYL)-BENZONITRILE
4-CYANO-4'-ETHOXYBIPHENYL
4-CYANO-4'-ETHYLOXYBIPHENYL
4-ETHOXY-4'-CYANOBIPHENYL
4'-ETHOXY-BIPHENYL-4-CARBONITRILE
AKOS BAR-2140
1’-biphenyl]-4-carbonitrile,4’-ethoxy-[
M6
4'-ethoxy[1,1'-biphenyl]-4-carbonitrile
4-Ethoxy-4'-Cyanobiphenyl,7CbC20H19N
4-(4''-N-ETHYLOXYBIPHENYL)-BENZONITRILE: 99.5%
4'-Ethoxy-4-cyanobiphenyl
4'-Ethoxy-4-biphenylcarbonitrile
[EINECS(EC#)]

261-417-3
[Molecular Formula]

C15H13NO
[MDL Number]

MFCD01218033
[Molecular Weight]

223.27
[MOL File]

58743-78-5.mol
Chemical PropertiesBack Directory
[Melting point ]

102 °C
[Boiling point ]

380.8±35.0 °C(Predicted)
[density ]

1.12±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

soluble in Toluene
[form ]

powder to crystal
[color ]

White to Almost white
[Usage]

Intermediates of Liquid Crystals
[InChI]

InChI=1S/C15H13NO/c1-2-17-15-9-7-14(8-10-15)13-5-3-12(11-16)4-6-13/h3-10H,2H2,1H3
[InChIKey]

VETJRGXWDLHERN-UHFFFAOYSA-N
[SMILES]

C1(C2=CC=C(OCC)C=C2)=CC=C(C#N)C=C1
[CAS DataBase Reference]

58743-78-5(CAS DataBase Reference)
[EPA Substance Registry System]

58743-78-5(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H302+H312+H332
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
[Risk Statements ]

22-36/37/38
[Safety Statements ]

26-36/37-60
[TSCA ]

TSCA listed
[HS Code ]

29269090
Hazard InformationBack Directory
[Chemical Properties]

white crystal
[Uses]

Intermediates of Liquid Crystals
[Synthesis]

4-Bromobenzonitrile

623-00-7

4-Ethoxyphenylboronic acid

22237-13-4

4-Ethoxy-[1,1'-biphenyl]-4'-carbonitrile

58743-78-5

General procedure for the synthesis of 4-ethoxy-4'-cyanobiphenyl from 4-bromobenzonitrile and 4-ethoxyphenylboronic acid: in typical experiments, a mixture of aryl bromide (0.50 mmol), phenylboronic acid (0.55 mmol), K2CO3 (1.5 mmol), 0.2 mol% of ligand, and 1 mol% of PdCl2(CH3CN)2 in 1.5 mL of ethanol was stirred. The reaction was carried out in air at 50 °C for 1.5 hours. Subsequently, the solvent ethanol was completely removed under vacuum at 0.09 MPa and 45 °C to give the crude product. Finally, the target product was isolated and purified by silica gel column chromatography.

[References]

[1] Journal of Materials Chemistry A, 2013, vol. 1, # 41, p. 12909 - 12918
[2] Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2017, vol. 87, # 1-2, p. 29 - 36
Spectrum DetailBack Directory
[Spectrum Detail]

4-Ethoxy-[1,1'-biphenyl]-4'-carbonitrile(58743-78-5)MS
4-Ethoxy-[1,1'-biphenyl]-4'-carbonitrile(58743-78-5)1HNMR
4-Ethoxy-[1,1'-biphenyl]-4'-carbonitrile(58743-78-5)13CNMR
4-Ethoxy-[1,1'-biphenyl]-4'-carbonitrile(58743-78-5)IR1
4-Ethoxy-[1,1'-biphenyl]-4'-carbonitrile(58743-78-5)IR2
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