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4-Bromobenzaldehyde

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4-Bromobenzaldehyde Basic information

Product Name:
4-Bromobenzaldehyde
Synonyms:
  • 4-Brombenzaldehyd
  • 4-bromo-benzaldehyd
  • Benzaldehyde, p-bromo-
  • Benzaldehyde,4-bromo-
  • p-bromo-benzaldehyd
  • AKOS BBS-00003194
  • 4-BROMOBENZYLALDEHYDE
  • 4-BROMOBENZALDEHYDE
CAS:
1122-91-4
MF:
C7H5BrO
MW:
185.02
EINECS:
214-365-0
Product Categories:
  • Pyridines ,Indolines ,Indoles
  • Aldehydes
  • FINE Chemical & INTERMEDIATES
  • Aromatic Aldehydes & Derivatives (substituted)
  • C7
  • Carbonyl Compounds
  • Benzaldehyde
  • Benzaldehyde (Building Blocks for Liquid Crystals)
  • Bifunctional Compounds (Building Blocks for Liquid Crystals)
  • Building Blocks for Liquid Crystals
  • Functional Materials
  • 1122-91-4
  • bc0001
Mol File:
1122-91-4.mol
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4-Bromobenzaldehyde Chemical Properties

Melting point:
55-58 °C(lit.)
Boiling point:
66-68°C 2mm
Density 
1.85 g/cm3
refractive index 
1.5727 (estimate)
Flash point:
228 °F
storage temp. 
Store below +30°C.
solubility 
Chloroform, Ethyl Acetate
form 
Crystalline Solid
color 
White
Water Solubility 
INSOLUBLE
Sensitive 
Air Sensitive
BRN 
507100
InChIKey
ZRYZBQLXDKPBDU-UHFFFAOYSA-N
LogP
2.75 at 25℃
CAS DataBase Reference
1122-91-4(CAS DataBase Reference)
NIST Chemistry Reference
Benzaldehyde, 4-bromo-(1122-91-4)
EPA Substance Registry System
Benzaldehyde, 4-bromo- (1122-91-4)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
22-36/37/38-43
Safety Statements 
26-36/37-36/37/39-22
RIDADR 
2811
WGK Germany 
2
RTECS 
CU4810000
Hazard Note 
Irritant/Harmful/Air Sensitive
TSCA 
Yes
HazardClass 
6.1(b)
PackingGroup 
III
HS Code 
29130000

MSDS

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4-Bromobenzaldehyde Usage And Synthesis

Chemical Properties

white crystalline solid

Uses

4-Bromobenzaldehyde is widely utilized as an intermediate for the preparation of agrochemicals, pharmaceuticals and other organic compounds. It is used as a precursor and reacts with sulfamethoxazole to prepare Schiff?s base, 4-[(4-Bromo-benzylidene)-amino]-N-(5-methyl-isoxazol-3-yl)-benzene sulfonamide, which can be used for the photo stability of polyvinyl chloride (PVC). It plays an important role in palladium-catalyzed mono- and bis-arylation of 3,4-(ethylenedioxy)thiophenes. It is employed in a cross-coupling study with potassium vinyltrifluoroborate.

Uses

Employed in palladium-catalyzed mono- and bis-arylation of 3,4-(ethylenedioxy)thiophenes. Also used in a cross-coupling study with potassium vinyltrifluoroborate.

Synthesis Reference(s)

Journal of the American Chemical Society, 81, p. 4113, 1959 DOI: 10.1021/ja01524a080
Tetrahedron Letters, 21, p. 813, 1980 DOI: 10.1016/S0040-4039(00)71512-7

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