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B34680

Sigma-Aldrich

Biphenyl-4-carboxaldehyde

99%

Synonym(s):

4-Phenylbenzaldehyde

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About This Item

Linear Formula:
C6H5C6H4CHO
CAS Number:
3218-36-8
Molecular Weight:
182.22
Beilstein:
606693
EC Number:
221-742-3
MDL number:
MFCD00006947
UNSPSC Code:
12352100
PubChem Substance ID:
24891721
NACRES:
NA.22

Quality Level

200

Assay

99%

form

crystals

bp

184 °C/11 mmHg (lit.)

mp

57-59 °C (lit.)

SMILES string

O=Cc1ccc(cc1)-c2ccccc2

InChI

1S/C13H10O/c14-10-11-6-8-13(9-7-11)12-4-2-1-3-5-12/h1-10H

InChI key

ISDBWOPVZKNQDW-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P301 + P312 + P330

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

352.0 - 381.9 °F

Flash Point(C)

177.8 - 194.4 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM4792
BCCK2456
BCCB6834
BCBZ6807
BCBS1639V

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Mariela M Nolasco et al.
Molecules (Basel, Switzerland), 25(6) (2020-03-22)
The present work emphasizes the value of periodic density functional theory (DFT) calculations in the assessment of the vibrational spectra of molecular crystals. Periodic calculations provide a nearly one-to-one match between the calculated and observed bands in the inelastic neutron
Yuki Okabe et al.
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 22(5), 713-725 (2017-01-14)
The construction of molecular catalysts that are active toward CO
Danuta Sek et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 175, 24-35 (2016-12-25)
The new Schiff bases bearing anthracene unit were synthesized from 2-aminoanthracene and various aldehydes such as: benzaldehyde, 4-(diphenylamino)benzaldehyde, 9-phenanthrenecarboxaldehyde, 9-anthracenecarboxaldehyde, and biphenyl-4-carboxaldehyde, 2-naphthaldehyde. Resulted azomethines were characterized by IR, NMR (
Sorel Jatunov et al.
Carbohydrate polymers, 123, 288-296 (2015-04-07)
A variety of fluorescent imino and secondary amino chitosans were synthesized under very mild conditions by reaction of the biopolymer amino functions with aromatic aldehydes in an acidified methanolic suspension. Simultaneous reactions of several aldehydes with chitosan were successfully carried

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