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112216

Sigma-Aldrich

4-Chlorobenzaldehyde

97%

Sinônimo(s):

p-Chlorobenzaldehyde

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About This Item

Fórmula linear:
ClC6H4CHO
Número CAS:
104-88-1
Peso molecular:
140.57
Beilstein:
385858
Número CE:
203-247-4
Número MDL:
MFCD00003379
Código UNSPSC:
12352100
eCl@ss:
39050405
ID de substância PubChem:
24847077
NACRES:
NA.22

Ensaio

97%

Formulário

solid

p.e.

213-214 °C (lit.)

pf

45-50 °C (lit.)

grupo funcional

aldehyde
chloro

cadeia de caracteres SMILES

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

InChI

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

chave InChI

AVPYQKSLYISFPO-UHFFFAOYSA-N

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Descrição geral

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.

Pictogramas

Exclamation markEnvironment
GHS07,GHS09

Palavra indicadora

Warning

Frases de perigo

H302,H315,H317,H319,H411

Classificações de perigo

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

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

197.6 °F - closed cup

Ponto de fulgor (°C)

92 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análise (COA)

Lot/Batch Number
STBK3721
STBJ7091
STBJ6342
STBJ5110
STBJ4612

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4-CHLORO-4'-METHOXYCHALCONE

4-Chlorobenzaldehyde dimethyl acetal 98%

Sigma-Aldrich

499110

4-Chlorobenzaldehyde dimethyl acetal

p-Tolualdehyde 97%

Sigma-Aldrich

T35602

p-Tolualdehyde

4-Chlorochalcone 97%

Sigma-Aldrich

558311

4-Chlorochalcone

4′-Chloroacetophenone 97%

Sigma-Aldrich

C19708

4′-Chloroacetophenone

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S525723

4-CHLORO-4'-METHYLCHALCONE

4'-CHLORO-4-METHOXYCHALCONE AldrichCPR

S547662

4'-CHLORO-4-METHOXYCHALCONE

4-Methylbenzaldehyde for synthesis

Sigma-Aldrich

8.06179

4-Methylbenzaldehyde

4-Chlorobenzaldehyde-2,3,5,6-d4 98 atom % D, 99% (CP)

Sigma-Aldrich

491535

4-Chlorobenzaldehyde-2,3,5,6-d4

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:
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)
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
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.
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