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B34680

Biphenyl-4-carboxaldehyde

Name: Biphenyl-4-carboxaldehyde
Brand: ALDRICH

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

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

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

Certificates of Analysis (COA)

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Syntheses and CO

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

New anthracene-based Schiff bases: Theoretical and experimental investigations of photophysical and electrochemical properties.

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 (

Fluorescent imino and secondary amino chitosans as potential sensing biomaterials.

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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