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METHYL 5-BROMOSALICYLATE

METHYL 5-BROMOSALICYLATE Suppliers list
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Products Intro: Product Name:METHYL 5-BROMOSALICYLATE
CAS:4068-76-2
Purity:99% Package:1KG;30USD|25KG;25USD|100KG;20USD
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Products Intro: Product Name:methyl 5-bromo-2-hydroxybenzoate
CAS:4068-76-2
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:Methyl 5-Bromosalicylate
CAS:4068-76-2
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METHYL 5-BROMOSALICYLATE manufacturers

METHYL 5-BROMOSALICYLATE Basic information
Product Name:METHYL 5-BROMOSALICYLATE
Synonyms:RARECHEM AL BF 0040;TIMTEC-BB SBB002397;AKOS BBB/379;5-BROMOSALICYLIC ACID METHYL ESTER;ASISCHEM D13384;AURORA KA-2528;BUTTPARK 41\07-02;METHYL 5-BROMOSALICYLATE
CAS:4068-76-2
MF:C8H7BrO3
MW:231.04
EINECS:223-776-4
Product Categories:Aromatic Esters;C8 to C9;Carbonyl Compounds;Esters
Mol File:4068-76-2.mol
METHYL 5-BROMOSALICYLATE Structure
METHYL 5-BROMOSALICYLATE Chemical Properties
Melting point 61-65 °C (lit.)
Boiling point 266.6±20.0 °C(Predicted)
density 1.627±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka9.19±0.18(Predicted)
form Solid
color White to pale brown
InChIInChI=1S/C8H7BrO3/c1-12-8(11)6-4-5(9)2-3-7(6)10/h2-4,10H,1H3
InChIKeyFJYDBKPPGRZSOZ-UHFFFAOYSA-N
SMILESC(OC)(=O)C1=CC(Br)=CC=C1O
CAS DataBase Reference4068-76-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HazardClass IRRITANT
HS Code 2918290090
MSDS Information
ProviderLanguage
SigmaAldrich English
METHYL 5-BROMOSALICYLATE Usage And Synthesis
UsesMethyl 5-bromosalicylate was used as starting reagent in the synthesis of immobilization precursor of photoswitchable piperidine base.
Synthesis
Methanol

67-56-1

5-Bromosalicylic acid

89-55-4

METHYL 5-BROMOSALICYLATE

4068-76-2

General procedure for the synthesis of methyl 5-bromosalicylate from methanol and 5-bromosalicylic acid: Step a) Synthesis of methyl 5-bromosalicylate: thionyl chloride (440 g, 3.7 mol) was slowly added to a solution of toluene (2 L) containing 5-bromosalicylic acid (200 g, 0.92 mol) at 0 °C and the reaction was stirred. The reaction mixture was then heated to 70 °C and refluxed for 40 hours. Upon completion of the reaction, the excess solvent was removed by distillation. Ethyl acetate (2 L) was added to the crude product for dissolution, and the organic layer was washed sequentially with 10% cold aqueous sodium bicarbonate (2 x 1 L) and brine, and then dried. Finally, the solvent was removed by vacuum to afford methyl 5-bromosalicylate as a low melting point solid (190 g, 89% yield). TLC conditions: petroleum ether/ethyl acetate (7:3), Rf value: 0.6.

References[1] Bioorganic and Medicinal Chemistry Letters, 2004, vol. 14, # 10, p. 2621 - 2625
[2] Journal of Materials Chemistry, 1996, vol. 6, # 8, p. 1297 - 1307
[3] Organic Letters, 2014, vol. 16, # 19, p. 5140 - 5143
[4] Patent: WO2005/12280, 2005, A1. Location in patent: Page/Page column 46-47
[5] Patent: WO2005/11685, 2005, A1. Location in patent: Page/Page column 41
Tag:METHYL 5-BROMOSALICYLATE(4068-76-2) Related Product Information
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