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2-(5-bromopyridin-2-yl)acetic acid

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CAS:192642-85-6
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CAS:192642-85-6
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2-(5-bromopyridin-2-yl)acetic acid manufacturers

2-(5-bromopyridin-2-yl)acetic acid Basic information
Product Name:2-(5-bromopyridin-2-yl)acetic acid
Synonyms:5-Bromopyridine-2-acetic acid;5-BroMopyridin-2-acetic acid;5-BroMo-2-pyridineacetic acid, 98%;(5-broMopyridin-2-yl)acetic acid;5-BroMo-2-pyridylacetic acid;2-(5-bromopyridin-2-yl)acetic acid;2-(5-Bromopyridin-2-yl)ethanoic acid, 5-Bromo-2-(carboxymethyl)pyridine;2-(5-Bromo-2-pyridyl)acetic Acid
CAS:192642-85-6
MF:C7H6BrNO2
MW:216.03
EINECS:
Product Categories:
Mol File:192642-85-6.mol
2-(5-bromopyridin-2-yl)acetic acid Structure
2-(5-bromopyridin-2-yl)acetic acid Chemical Properties
Melting point 120-123℃
Boiling point 326.2±27.0 °C(Predicted)
density 1.710±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
form powder
pka3.81±0.10(Predicted)
AppearanceLight yellow to yellow Solid
InChIInChI=1S/C7H6BrNO2/c8-5-1-2-6(9-4-5)3-7(10)11/h1-2,4H,3H2,(H,10,11)
InChIKeyATKULCGQSLCGEK-UHFFFAOYSA-N
SMILESC1(CC(O)=O)=NC=C(Br)C=C1
CAS DataBase Reference192642-85-6
Safety Information
Hazard Codes Xn
Risk Statements 22-41
Safety Statements 26-39
WGK Germany 3
HazardClass IRRITANT
HS Code 2933399990
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Dam. 1
MSDS Information
2-(5-bromopyridin-2-yl)acetic acid Usage And Synthesis
Synthesis
DIETHYL(5-BROMOPYRIDIN-2-YL)MALONATE

1215098-80-8

2-(5-bromopyridin-2-yl)acetic acid

192642-85-6

General procedure for the synthesis of 2-(5-bromopyridin-2-yl)acetic acid from diethyl malonate: In Example 40, diethyl 2-(5-bromopyridin-2-yl)-malonate (16.6 g, 52.5 mmol) was dissolved in methanol (200 mL) followed by addition of 2N aqueous sodium hydroxide solution (105 mL, 210 mmol). The reaction mixture was stirred at room temperature for 3 h, after which the solvent was removed by vacuum concentration. The residue was dissolved in water and neutralized with 2N hydrochloric acid to pH 3-4. Subsequently, the solid formed was collected by filtration, washed sequentially with water and ether, and dried to give a white solid product that did not require further purification (9.0 g, 80% yield). Results of mass spectrometry analysis: calculated value 215 (MH+), measured value 215 (MH+).

References[1] Patent: US2010/69328, 2010, A1. Location in patent: Page/Page column 36
[2] Patent: WO2016/34673, 2016, A1. Location in patent: Page/Page column 100
[3] Patent: WO2014/53967, 2014, A1. Location in patent: Page/Page column 160; 161
2-(5-bromopyridin-2-yl)acetic acid Preparation Products And Raw materials
Raw materialsDIETHYL(5-BROMOPYRIDIN-2-YL)MALONATE-->Sodium hydroxide-->Water-->Methanol-->Hydrochloric acid
Tag:2-(5-bromopyridin-2-yl)acetic acid(192642-85-6) Related Product Information
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