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B57400

Sigma-Aldrich

4-Bromobenzaldehyde

ReagentPlus®, 99%

Sinônimo(s):

1-Bromo-4-formylbenzene, 4-Bromobenzaldehyde, 4-Bromobenzenealdehyde, 4-Formyl-1-bromobenzene, 4-Formylbromobenzene, 4-Formylphenyl bromide, p-Bromobenzaldehyde, p-Formylbromobenzene

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About This Item

Fórmula linear:
BrC6H4CHO
Número CAS:
1122-91-4
Peso molecular:
185.02
Beilstein:
507100
Número CE:
214-365-0
Número MDL:
MFCD00003377
Código UNSPSC:
12352100
ID de substância PubChem:
24891856
NACRES:
NA.22

linha de produto

ReagentPlus®

Ensaio

99%

Formulário

crystals

pf

55-58 °C (lit.)

cadeia de caracteres SMILES

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

InChI

1S/C7H5BrO/c8-7-3-1-6(5-9)2-4-7/h1-5H

chave InChI

ZRYZBQLXDKPBDU-UHFFFAOYSA-N

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Aplicação

4-Bromobenzaldehyde can be used as a reactant:
  • To synthesize vinyl esters by reacting with terminal alkynoates in the presence of triphenylphosphine catalyst.
  • In the palladium-catalyzed Mizoroki-Heck Cross-coupling reaction with styrene to synthesize arylated olefins.
  • In the Suzuki-Wittig reaction with formylphenylboronic acids to synthesize dimethyl biphenyl-diacrylates.

Informações legais

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H302,H315,H317,H319,H335

Classificações de perigo

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

228.2 °F - closed cup

Ponto de fulgor (°C)

109 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificados de análise (COA)

Lot/Batch Number
WXBD2523V
WXBD1571V
WXBD0893V
WXBC9374V
WXBC8917V

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Gary A Molander et al.
The Journal of organic chemistry, 71(26), 9681-9686 (2006-12-16)
We have previously reported that the palladium-catalyzed cross-coupling reaction of potassium vinyltrifluoroborate with aryl electrophiles proceeds with good yields. Herein, we describe recent progress in optimizing the reaction, as well as outlining the scope and limitations of the reaction. The
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The Ni-metallated porphyrin-based tetraphosphonic acid (Ni-tetra(4-phosphonophenyl)porphyrin, Ni-H8TPPP) was used for the synthesis of highly porous metal phosphonates containing the tetravalent cations Zr4+ and Hf4+. The compounds were thoroughly characterized regarding their sorption properties towards N2 and H2O as well as
Gugu Kubheka et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 191, 357-364 (2017-10-22)
The optical limiting (OL) properties of 3,5-dipyrenylvinyleneBODIPY dyes that contain both electron withdrawing and donating moieties have been investigated by using the z-scan technique at 532nm in the nanosecond pulse range. The extension of the π-conjugation at the 3,5-positions with
Ved Vati Singh et al.
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The metastable tetragonal Cu2Se phase as nanoflakes has been synthesized for the first time by treating CuCl2 taken in a mixture (1:1) of 1-octadecene and oleylamine with H2N-(CH2)3-SePh dissolved in 1-octadecene. Powder X-ray diffraction (PXRD), HRTEM, SEM-EDX and XPS have

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