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4-Bromocinnamaldehyde

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4-Bromocinnamaldehyde Basic information
Product Name:4-Bromocinnamaldehyde
Synonyms:4-BROMOCINNAMALDEHYDE;2-PROPENAL, 3-(4-BROMOPHENYL)-,(2E);(E)-3-(4-Bromophenyl)propenal;(E)-4-Bromocinnamaldehyde;4-Bromo-trans-cinnamaldehyde;E-3-(4-Bromophenyl)-2-propenal;3-(4-broMophenyl)acrylaldehyde;trans-4-Bromocinnamaldehyde >
CAS:49678-04-8
MF:C9H7BrO
MW:211.06
EINECS:
Product Categories:aldehydes;Miscellaneous Reagents
Mol File:49678-04-8.mol
4-Bromocinnamaldehyde Structure
4-Bromocinnamaldehyde Chemical Properties
Melting point 70-74°C
Boiling point 310.5±17.0 °C(Predicted)
density 1.466±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
solubility Chloroform, Dichloromethane, Ethyl Acetate, Hexane
form Solid
color Light Yellow
λmax298nm(CHCl3)(lit.)
InChI1S/C9H7BrO/c10-9-5-3-8(4-6-9)2-1-7-11/h1-7H/b2-1+
InChIKeyXYRAWLRFGKLUMW-OWOJBTEDSA-N
SMILESBrc1ccc(\C=C\C=O)cc1
CAS DataBase Reference49678-04-8
Safety Information
Safety Statements 22-24/25
WGK Germany 3
HS Code 2913.00.4000
Storage Class11 - Combustible Solids
MSDS Information
4-Bromocinnamaldehyde Usage And Synthesis
Chemical PropertiesLight Yellow Solid
Synthesis
1-Bromo-4-cyclopropylbenzene

1124-14-7

4-Bromocinnamaldehyde

49678-04-8

Isoxazole, 5-(4-bromophenyl)-4,5-dihydro-

90712-56-4

GENERAL METHOD: Sodium nitrite (0.69 g, 0.01 mol) was added in batches over 10-15 min to a mixture containing 0.01 mol arylcyclopropane (1a-1l), trifluoroacetic acid (5.2 g) and chloroform (15 mL).The reaction mixture was cooled and then slowly heated up to 20°C and maintained at that temperature for 1 hr. Upon completion of the reaction, the mixture was poured into 100 mL of cold water. The organic phase was separated and the aqueous phase was extracted with chloroform (2 x 10 mL), the organic phase and the extract were combined and subsequently washed with water (2 x 30 mL) and dried with anhydrous magnesium sulfate. The solvent was removed under reduced pressure and the residue was analyzed by 1H NMR. The target compound 21 was purified by crystallization. The exact composition of the reaction mixture is detailed in Table 1.The physical constants and spectral data of the obtained compounds 2a [16], 2b [30] and 21 [28] are in agreement with the literature reports.

References[1] Russian Journal of Organic Chemistry, 2016, vol. 52, # 3, p. 397 - 403
[2] Zh. Org. Khim., 2016, vol. 52, # 3, p. 417 - 423,7
4-Bromocinnamaldehyde Preparation Products And Raw materials
Raw materials1-Bromo-4-cyclopropylbenzene-->Trifluoroacetic acid-->Sodium nitrite-->Chloroform
Tag:4-Bromocinnamaldehyde(49678-04-8) Related Product Information
4-Bromomethylbenzoic acid alpha-Hexylcinnamaldehyde 3-(trifluoromethyl) Cinnamaldehyde 4-Bromobenzoic acid trans,trans-2,4-Undecadienal Cinnamaldehyde 4-Bromophenol 4-Pentylbromobenzene α-Methylcinnamaldehyde 4'-Bromoacetophenone α-Bromocinnamaldehyde 4-Bromo-2-fluorocinnamic acid 4'-BROMOFLAVONE ETHYL TRANS-4-BROMOCINNAMATE 4-Bromocinnamic acid trans-3-Bromocinnamaldehyde,3-BROMOCINNAMALDEHYDE trans-Cinnamaldehyde 4-(4-BROMO-PHENYL)-BUT-3-EN-2-ONE