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112216

Sigma-Aldrich

4-Chlorobenzaldehyde

97%

Sinónimos:

p-Chlorobenzaldehyde

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About This Item

Fórmula lineal:
ClC6H4CHO
Número de CAS:
104-88-1
Peso molecular:
140.57
Beilstein/REAXYS Number:
385858
EC Number:
203-247-4
MDL number:
MFCD00003379
UNSPSC Code:
12352100
eCl@ss:
39050405
PubChem Substance ID:
24847077
NACRES:
NA.22

assay

97%

form

solid

bp

213-214 °C (lit.)

mp

45-50 °C (lit.)

functional group

aldehyde

SMILES string

[H]C(=O)c1ccc(Cl)cc1

InChI

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

InChI key

AVPYQKSLYISFPO-UHFFFAOYSA-N

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General description

4-Chlorobenzaldehyde reacts with 3-tert-butyl-N-4-chlorobenzyl-1-phenyl-1H-pyrazol-5-amine to form (E)-3-tert-Butyl-4-(4-chlorobenzyl)-N-(4-chlorobenzylidene)-1-phenyl-1H-pyrazol-5-amine by a microwave-mediated reaction.

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

197.6 °F - closed cup

flash_point_c

92 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Jairo Quiroga et al.
Acta crystallographica. Section C, Crystal structure communications, 69(Pt 9), 1039-1042 (2013-09-06)
The title compound, C27H25Cl2N3, is an unexpected but high-yield product from the microwave-mediated reaction between 3-tert-butyl-N-4-chlorobenzyl-1-phenyl-1H-pyrazol-5-amine and 4-chlorobenzaldehyde. Inversion-related pairs of molecules are linked by C-H···π(arene) hydrogen bonds to form cyclic centrosymmetric dimers, and dimers of this type are linked
[Experimental substantiation of an approximate safe level of p-chlorobenzaldehyde in the air of the work area].
A I Khalepo et al.
Gigiena truda i professional'nye zabolevaniia, (2)(2), 50-51 (1987-02-01)
Mohammed M Rahman et al.
Designed monomers and polymers, 21(1), 82-98 (2018-05-31)
A new category of thermally stable hybrid polyarylidene(azomethine-ether)s and copolyarylidene(azomethine-ether)s (PAAP) based on diarylidenecycloalkanones has been synthesized using solution polycondensation method. For potential cationic sensor development, a thin layer of PAAP onto a flat glassy carbon electrode (GCE, surface area:
M Reza Naimi-Jamal et al.
Molecular diversity, 14(3), 473-477 (2010-04-08)
Solvent-free one-pot synthesis of 2-amino-4H-chromene scaffold is described in a very simple, efficient, and environmentally benign method using sodium carbonate as a cheap and non-toxic catalyst with up to excellent yields.
Divya P Narayanan et al.
Journal of colloid and interface science, 520, 70-80 (2018-03-13)
A one pot synthesis of carbon dot incorporated porous coconut shell char derived sulphonated catalyst is reported here for the first time and is effectively used in the multicomponent synthesis of amidoalkyl naphthol. Macroporous nature of the char is revealed
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