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Merck
CN

C23403

3-Chlorobenzaldehyde

97%

Synonym(s):

3-Chlorobenzaldehyde, 3-Chlorophenylcarboxaldehyde, m-Chlorobenzaldehyde, m-Chlorobenzenecarboxaldehyde

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About This Item

Linear Formula:
ClC6H4CHO
CAS Number:
587-04-2
Molecular Weight:
140.57
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24892318
EC Number:
209-596-9
Beilstein/REAXYS Number:
507098
MDL number:
MFCD00003350
Assay:
97%
Form:
liquid

Key Documents

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InChI key

SRWILAKSARHZPR-UHFFFAOYSA-N

InChI

1S/C7H5ClO/c8-7-3-1-2-6(4-7)5-9/h1-5H

SMILES string

[H]C(=O)c1cccc(Cl)c1

assay

97%

form

liquid

Quality Level

100

bp

213-214 °C (lit.)

mp

9-12 °C (lit.)

density

1.241 g/mL at 25 °C (lit.)

Related Categories

General description

3-Chlorobenzaldehyde is commonly used as a key building block in the synthesis of Schiff base ligands.

Storage Class

10 - Combustible liquids

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

wgk

WGK 2

flash_point_f

190.4 °F - closed cup

flash_point_c

88 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
STBL0613
STBK6179
STBJ3143
STBH5535
STBF5569V

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Synthesis and characterization of Cu (II), Co (II), Ni (II), Au (III), complexes with (Z)-1-(4-((3-chlorobenzylidene) amino) phenyl) ethan-1-one ligand
GS Al-Obaidy, et al.
Drug Invention Today, 13 (2020)
Yoon S Song et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 38(3), 513-531 (2021-02-05)
The migration of small molecular mass organic compounds from polypropylene (PP) copolymer films into food simulants during and after high pressure processing (HPP) was studied. An overlapping temperature profile was developed to isolate the pressure effect of HPP (700 MPa, 71°C
Adnan Ashraf et al.
European journal of medicinal chemistry, 159, 282-291 (2018-10-09)
Chalcones and 1,2-benzothiazines are two important classes of bioactive compounds, each scaffold endowed with diverse pharmacological activities. Combining both of these pharmacophores in a single molecule was aimed to yield multi-modal agents. Herein, we report a series of hybrid compounds

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