3,5-Dibromosalicylaldehyde

3,5-Dibromosalicylaldehyde Basic information
Product Name:3,5-Dibromosalicylaldehyde
Synonyms:LABOTEST-BB LT00137784;3,5-DIBROMO-2-HYDROXYBENZALDEHYDE;3,5-DIBROMOSALICYLADEHYDE;3,5-DIBROMOSALICYLALDEHYDE;3,5-DIBROMOSILICYLALDEHYDE;SALOR-INT L497649-1EA;OTAVA-BB BB7018801957;AKOS BBS-00003256
CAS:90-59-5
MF:C7H4Br2O2
MW:279.91
EINECS:202-003-4
Product Categories:Aldehydes;C7;Carbonyl Compounds;Aromatic Aldehydes & Derivatives (substituted);Benzaldehyde;Adehydes, Acetals & Ketones;Bromine Compounds;Phenols
Mol File:90-59-5.mol
3,5-Dibromosalicylaldehyde Structure
3,5-Dibromosalicylaldehyde Chemical Properties
Melting point 82-83.5 °C (lit.)
Boiling point 261.2±35.0 °C(Predicted)
density 1.9661 (rough estimate)
refractive index 1.4970 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility methanol: soluble25mg/mL, clear, yellow to brown
form Crystalline Powder
pka6.08±0.23(Predicted)
color Yellow to yellow-brown
Water Solubility Soluble in methanol 25 mg/mL. Insoluble in water.
Sensitive Air Sensitive
Merck 14,3027
BRN 1424739
InChIKeyJHZOXYGFQMROFJ-UHFFFAOYSA-N
CAS DataBase Reference90-59-5(CAS DataBase Reference)
NIST Chemistry Reference3,5-Dibromosalicylaldehyde(90-59-5)
EPA Substance Registry SystemBenzaldehyde, 3,5-dibromo-2-hydroxy- (90-59-5)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39-24/25
RIDADR UN 3077 9 / PGIII
WGK Germany 3
RTECS CU5609000
HazardClass 9
PackingGroup III
HS Code 29130000
MSDS Information
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3,5-Dibromo-2-hydroxybenzaldehyde English
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ACROS English
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3,5-Dibromosalicylaldehyde Usage And Synthesis
Chemical Propertiesyellow to yellow-brown crystalline powder
Uses3,5-Dibromosalicylaldehyde reacts with alkyl cyanoacetates in the presence of ammonium acetate to yield 4H- chromenes. It can be used in the synthesis of Schiff base and can be used as reactant for synthesis of Schiff base ligands which forms mononuclear complexes with copper(II), nickel(II), zinc(II) and cobalt(II).
General Description3,5-Dibromosalicylaldehyde reacts with alkyl cyanoacetates in the presence of ammonium acetate to yield 4H- chromenes.
4-benzyl-3,5-dibromo-2,6-dihydroxy-benzoic acid 3,5-DIBROMO-2-METHOXYBENZOIC ACID 4,5-Dibromosalicylaldehyde 3,5-DIBROMO-2,4-DIHYDROXYBENZALDEHYDE 3',5'-Dibromo-2'-hydroxypropiophenone 2-((3,5-Dibromo-2,6-dimethoxybenzamido)methyl)-1-ethylpyrrolidine hydr ochloride METHYL 3,5-DIBROMO-2-METHOXYBENZOATE 6,8-DIBROMO-3-FORMYLCHROMONE, 99% 6,8-Dibromo-2-thio-2H-1,3-benzoxazine-2,4(3H)-dione 3,5-DIBROMO-2-ETHOXYBENZALDEHYDE AKOS B005945 3,5-DIBROMOSALICYLAMIDE 4'-CHLORO-6,8-DIBROMOFLAVONE 3',5'-Dibromo-2'-hydroxyacetophenone 3,5-DIBROMO-2-HYDROXY-4-METHOXYBENZALDEHYDE 6,8-DIBROMOFLAVONE 3,5-Dibromosalicylaldehyde oxime PHENYL 3,5-DIBROMO-2-HYDROXYBENZOATE

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