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Merck

B57001

Sigma-Aldrich

2-Bromobenzaldehyde

98%

Sinónimos:

2-Formylbromobenzene

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About This Item

Fórmula lineal:
BrC6H4CHO
Número de CAS:
Peso molecular:
185.02
Beilstein/REAXYS Number:
636132
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

98%

form

liquid

refractive index

n20/D 1.595 (lit.)

bp

230 °C (lit.)

mp

16-19 °C (lit.)

density

1.585 g/mL at 25 °C (lit.)

SMILES string

Brc1ccccc1C=O

InChI

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

InChI key

NDOPHXWIAZIXPR-UHFFFAOYSA-N

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General description

2-Bromobenzaldehyde is a versatile building block used in Suzuki-Miyaura and Buchwald-Hartwig reactions, cross-coupling reactions to form carbon-carbon or carbon-heteroatom bonds

Application

Synthetic applications of 2-bromobenzaldehyde include:
  • Synthesis of aza-fused polycyclic quinolines through copper-catalyzed cascade reaction.
  • Preparation of 1-substituted indazoles by CuI-catalyzed coupling with N-aryl hydrazides.
  • It is a key starting material in the total synthesis of an anticancer agent, (-)-taxol.
  • Palladium/copper-catalyzed coupling and cyclization of terminal acetylenes derived from 2-bromobenzaldehyde and unsaturated imines can be used in the synthesis of wide range of isoquinolines, including decumbenine B.
  • Fluoren-9-ones can be synthesized by annulation of arynes, generated in situ from 2-(trimethylsilyl)aryl triflates, with 2-bromobenzaldehyde in the presence of palladium(0) catalyst.
  • It can also be used to build a variety of steroid frameworks, in which ring A is derived from 2-bromobenzaldehyde.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

203.0 °F - closed cup

flash_point_c

95 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Los clientes también vieron

Palladium-catalyzed one-pot Suzuki-Miyaura cross coupling followed by oxidative lactonization: a novel and efficient route for the one-pot synthesis of benzo [c] chromene-6-ones
R Singha, et al.
Tetrahedron Letters, 54, 657-660 (2013)
Synthesis of aza-fused polycyclic quinolines through copper-catalyzed cascade reactions.
Cai Q, et al.
Organic Letters, 12(7), 1500-1503 (2010)
A gold-catalyzed domino process to the steroid framework.
Hildebrandt D and Dyker G
The Journal of Organic Chemistry, 71(18), 6728-6733 (2006)
Enantioselective total synthesis of (?)-taxol.
Kusama H, et al.
Journal of the American Chemical Society, 122(16), 3811-3820 (2000)
Assembly of N, N-Disubstituted Hydrazines and 1-Aryl-1 H-indazoles via Copper-Catalyzed Coupling Reactions.
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Organic Letters, 14(10), 2552-2555 (2012)

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