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3,5-Dibromobenzaldehyde

CAS No.
56990-02-4
Chemical Name:
3,5-Dibromobenzaldehyde
Synonyms
DBBA;3,5-DIBROMOBENZALDEHYDE;Benzaldehyde, 3,5-dibromo-;3,5-Dibromobenzaldehyde>3,5-Dibromobenzaldehyde,98%;3,5-DIBROMOBENZALDEHYDE 98%;3,5-Dibromobenzaldehyde//DBBA;3,5-dibromophenylformaldehyde;METHYL3,5-DIBROMOPHENYLACETATE;3,5-Dibromobenzaldehyde97%MinByG.C
CBNumber:
CB4253350
Molecular Formula:
C7H4Br2O
Molecular Weight:
263.91
MDL Number:
MFCD00156887
MOL File:
56990-02-4.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 02:30:53

3,5-Dibromobenzaldehyde Properties

Melting point 84-88 °C (lit.)
Boiling point 287.2±20.0 °C(Predicted)
Density 1.977±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility soluble in DMSO, Ethyl Acetate, Methanol
form Powder or Crystals
color White to light beige
Water Solubility insoluble
Sensitive Air Sensitive
BRN 2573432
InChI InChI=1S/C7H4Br2O/c8-6-1-5(4-10)2-7(9)3-6/h1-4H
InChIKey ZLDMZIXUGCGKMB-UHFFFAOYSA-N
SMILES C(=O)C1=CC(Br)=CC(Br)=C1
CAS DataBase Reference 56990-02-4(CAS DataBase Reference)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)
GHS05
Signal word  Danger
Hazard statements  H314
Precautionary statements  P260-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338-P363
PPE Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  C
Risk Statements  34
Safety Statements  26-36/37/39-45
RIDADR  UN 3261 8/PG 2
WGK Germany  3
HazardClass  8
PackingGroup 
HS Code  29130000
Storage Class 8A - Combustible corrosive hazardous materials
Hazard Classifications Skin Corr. 1B
NFPA 704
1
2 0

3,5-Dibromobenzaldehyde price More Price(80)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 515396 3,5-Dibromobenzaldehyde 56990-02-4 5g $87.3 2026-04-30 Buy
TCI Chemical D2832 3,5-Dibromobenzaldehyde >97.0%(GC) 56990-02-4 5g $66 2026-04-30 Buy
TCI Chemical D2832 3,5-Dibromobenzaldehyde >97.0%(GC) 56990-02-4 25g $263 2026-04-30 Buy
Usbiological 272976 3,5-Dibromobenzaldehyde Asreported 56990-02-4 5g $347 2026-06-03 Buy
Usbiological 272976 3,5-Dibromobenzaldehyde Asreported 56990-02-4 10g $489 2026-06-03 Buy
Product number Packaging Price Buy
515396 5g $87.3 Buy
D2832 5g $66 Buy
D2832 25g $263 Buy
272976 5g $347 Buy
272976 10g $489 Buy

3,5-Dibromobenzaldehyde Chemical Properties,Uses,Production

Description

3,5-Dibromobenzaldehyde is a white or beige solid with a melting point of 84-88 °C. Its boiling point and density are estimated to be 287.2±20.0 °C and 1.977±0.06 g/cm3, respectively. It is insoluble in water.

Synthesis

1,3,5-tribromobenzene (3.01 g, 9.6 mmol) in diethyl ether (80 mL) was cooled to -78°C followed by the addition of one equivalent of n-BuLi dropwise (2.5 M, 3.8 mL). The reaction was stirred for 30 minutes then DMF (740 µL, 9.6 mmol) was added dropwise to the reaction and stirred at -78°C for one hour. The vessel was then placed in an ice bath and stirred for 30 minutes. A 10% HCl solution (100 mL) was added to quench the reaction followed by CHCl3 (150 mL). The organic layer was collected and the aqueous layer washed with CHCl3 (80 mL). The organic layers where combined and dried over MgSO4 and the solvent removed. The crude product was purified by column chromatography eluting with 10% EtOAc in hexanes. Spectral data for the title compound was not reported in the literature reference. Yield: 1.93 g of the title compound (77%). 1H NMR (CDCl3, 300 MHz): δ = 9.90 (s, 1H), 7.92 (d, 2H), 7.60 (s, 1H); 13C NMR (CDCl3, 75 MHz) δ = 189.3, 139.7, 139.0, 131.37, 124.1; GC-MS [M+H]+ 262.8709, calcd 262.8707
3,5-Dibromobenzaldehyde

Uses

3,5-Dibromobenzaldehyde is a dibrominated benzaldehyde that is a very useful building block for the preparation of a wide range of biologically active compounds such as a antibacterials. The non-AIE active compound 3,5-dibromobenzaldehyde (DBB) could be used as the core to synthesize AIE luminogens, which differs from the traditional synthetic methods that are heavily dependent on the AIE active core. The three obtained DBB derivatives (S1, S2 and S3) displayed typical AIE features in which the quantum efficiencies of the solid film state were much higher than their solution state. The emission of these DBB derivatives could be fine-tuned by varying the substituents on the DBB rings[1].

Application

Reactant involved in:
Suzuki-Miyaura cross-coupling reactions
Synthesis of blue fluorescent dye derivatives for organic light emitting diodes
Sharpless kinetic resolution for the formation of Baylis-Hillman enal adducts
Synthesis of podophyllotoxin mimetic pyridopyrazoles as anticancer agents
Allylic alkylation
Synthesis of C2-symmetric biphosphine ligand I

References

[1] Kuang, Yunsuo et al. “Novel AIEgens with a 3,5-dibromobenzaldehyde skeleton: molecular design, synthesis, tunable emission and detection application.” Analytical Methods 46 (2018): 5486–5492.

56908-88-4
56990-02-4
Synthesis of 3,5-Dibromobenzaldehyde from 3,5-Dibromobenzyl bromide
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3,5-Dibromobenzaldehyde97%MinByG.C 3,5-Dibromobenzaldehyde,98% 3,5-DIBROMOBENZALDEHYDE 3,5-DIBROMOBENZALDEHYDE 98% METHYL3,5-DIBROMOPHENYLACETATE 3,5-Dibromobenzaldehyde> Benzaldehyde, 3,5-dibromo- 3,5-dibromophenylformaldehyde 3,5-Dibromobenzaldehyde//DBBA DBBA 56990-02-4 52990-02-4 56880-02-4 Br2C6H3CHO Building Blocks for Dendrimers C7 Carbonyl Compounds Building Blocks Aldehydes Organic Building Blocks intermediate fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis, functional materials, Aromatic Aldehydes OLED Functional Materials Aldehydes C7 Carbonyl Compounds Aromatic Aldehydes & Derivatives (substituted) Benzaldehyde Adehydes, Acetals & Ketones Bromine Compounds Building Blocks for Dendrimers