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3-BROMO-5-CHLORO-BENZALDEHYDE

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Company Name: Hebei Chuanghai Biotechnology Co., Ltd
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Products Intro: Product Name:3-BROMO-5-CHLORO-BENZALDEHYDE
CAS:188813-05-0
Purity:99% Package:1KG;0.00;USD|25KG;0.00;USD
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CAS:188813-05-0
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CAS:188813-05-0
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Products Intro: Product Name:3-Bromo-5-chlorobenzaldehyde
CAS:188813-05-0
Purity:98%(Min,GC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:3-BROMO-5-CHLORO-BENZALDEHYDE
CAS:188813-05-0
Purity:99% Package:1KG,5KG,10KG

3-BROMO-5-CHLORO-BENZALDEHYDE manufacturers

3-BROMO-5-CHLORO-BENZALDEHYDE Basic information
Product Name:3-BROMO-5-CHLORO-BENZALDEHYDE
Synonyms:3-BROMO-5-CHLORO-BENZALDEHYDE;3-Bromo-5-chlorobenzladehyde;5-Chloro-3-bromobenzaldehyde;3-BroMo-5-chlorobenzaldehyde, 98%+;3-Bromo-5-chL;Benzaldehyde, 3-bromo-5-chloro-;CAS:188813-05-0;3-BROMO-5-CHLORO-BENZALDEHYDE 7651/500ghh
CAS:188813-05-0
MF:C7H4BrClO
MW:219.46
EINECS:
Product Categories:C7Chemical Synthesis;Aldehydes;Carbonyl Compounds;New Products for Chemical Synthesis;Organic Building Blocks
Mol File:188813-05-0.mol
3-BROMO-5-CHLORO-BENZALDEHYDE Structure
3-BROMO-5-CHLORO-BENZALDEHYDE Chemical Properties
Melting point 68-73 °C
Boiling point 264.0±20.0 °C(Predicted)
density 1.698±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility soluble in Methanol
form powder to crystal
color White to Light yellow
InChIInChI=1S/C7H4BrClO/c8-6-1-5(4-10)2-7(9)3-6/h1-4H
InChIKeyJGMGDYUVFBBCEQ-UHFFFAOYSA-N
SMILESC(=O)C1=CC(Cl)=CC(Br)=C1
Safety Information
Hazard Codes Xn,N
Risk Statements 36/37/38-51/53-22
Safety Statements 26-36/37/39-61-53
RIDADR UN 3077 9/PG 3
WGK Germany 3
HS Code 2913000090
Storage Class13 - Non Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
3-BROMO-5-CHLORO-BENZALDEHYDE Usage And Synthesis
Chemical Propertieswhite crystal powder
Synthesis
1,3-Dibromo-5-chlorobenzene

14862-52-3

N,N-Dimethylformamide

68-12-2

3-BROMO-5-CHLORO-BENZALDEHYDE

188813-05-0

Under nitrogen protection, 3,5-dibromochlorobenzene (27 g, 100 mmol) was dissolved in anhydrous isopropyl ether (300.0 mL) in a dry flask. The reaction mixture was cooled to -78 °C and stirred continuously under nitrogen atmosphere. A 2.6 M hexane solution of n-butyllithium (40 mL, 100 mmol) was slowly added dropwise to the above solution. After the dropwise addition was completed, the reaction mixture was continued to be stirred at -78 °C for 30 minutes. Subsequently, N,N-dimethylformamide (DMF, 7.5 g, 100 mmol) was added dropwise while keeping the temperature below -78 °C. After the reaction was completed, 80 mL of ammonium chloride solution was added to the mixture and stirring was continued for 15 minutes. The ether layer was separated, washed sequentially with water (2 x 250 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. Finally, the crude product was purified by silica gel fast column chromatography to afford the target compound 3-bromo-5-chlorobenzaldehyde (16 g, 67% yield).

References[1] Patent: WO2014/15054, 2014, A1. Location in patent: Page/Page column 174; 190
3-BROMO-5-CHLORO-BENZALDEHYDE Preparation Products And Raw materials
Raw materials1,3-Dibromo-5-chlorobenzene-->N,N-Dimethylformamide-->Diisopropyl ether-->Hexane-->n-Butyllithium
Preparation Products2-(3-broMo-5-chlorophenyl)-4,6-diphenyl-1,3,5-triazine
Tag:3-BROMO-5-CHLORO-BENZALDEHYDE(188813-05-0) Related Product Information
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