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124974

Sigma-Aldrich

2-Chlorobenzaldehyde

99%

Sinônimo(s):

o-Chlorobenzaldehyde

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About This Item

Fórmula linear:
ClC6H4CHO
Número CAS:
Peso molecular:
140.57
Beilstein:
385877
Número CE:
Número MDL:
Código UNSPSC:
12352100
eCl@ss:
39050404
ID de substância PubChem:
NACRES:
NA.22

densidade de vapor

4.84 (vs air)

pressão de vapor

1.27 mmHg ( 50 °C)

Ensaio

99%

temperatura de autoignição

746 °F

índice de refração

n20/D 1.566 (lit.)

pb

209-215 °C (lit.)

pf

9-11 °C (lit.)

densidade

1.248 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

[H]C(=O)c1ccccc1Cl

InChI

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

chave InChI

FPYUJUBAXZAQNL-UHFFFAOYSA-N

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Descrição geral

2-Chlorobenzaldehyde undergoes alkynylation with phenylacetylene in the presence of catalytic ligands and dimethylzinc at 0°C to form binaphthyl-derived amino alcohols.

Aplicação

2-Chlorobenzaldehyde has been used in generation of small focused library of diversely functionalized dihydropyrimidine derivatives via one-pot three-component Biginelli cyclocondensation of β-ketoesters, aldehydes and thioureas.

Pictogramas

CorrosionExclamation mark

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

206.6 °F - closed cup

Ponto de fulgor (°C)

97 °C - closed cup

Equipamento de proteção individual

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Enantioselective alkynylation of aromatic aldehydes catalyzed by new chiral amino alcohol-based ligands.
Lu G, et al.
Tetrahedron Asymmetry, 12(15), 2147-2152 (2001)
M Rogojerov et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 61(7), 1661-1670 (2005-04-12)
Vibrational analysis of the two conformers of furfural and 2-chlorobenzaldehyde has been carried out on the basis of their IR and Raman spectra measured in isotropic and anisotropic (nematic liquid crystalline) solvent. The average orientation of the individual conformers in
E Schmid et al.
Mutagenesis, 6(4), 303-305 (1991-07-01)
The aneuploidy inducing capacity of 2-chlorobenzylidene malonitrile (CS), a chemical used as a riot control agent, and its hydrolysis products o-chlorobenzaldehyde and malonitrile was studied at various exposure conditions in V79 Chinese hamster cells. Chromosomes were counted in metaphase preparations
Doris Dallinger et al.
Nature protocols, 2(7), 1713-1721 (2007-07-21)
Here we report the generation of a small focused library of 12 diversely functionalized dihydropyrimidine (DHPM) derivatives via one-pot three-component Biginelli cyclocondensation of beta-ketoesters, aldehydes and (thio)ureas. By applying controlled microwave heating under sealed vessel conditions using a fully automated
Th Gomti Devi et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 62(4-5), 972-979 (2005-06-14)
The analysis of Raman anisotropy shift as a function of solvent concentration shows the weakening of pair interaction of the molecules due to the influence of solvent-induced perturbations. The present study deals with the effect of dielectric constant of the

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