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3-(3-CHLOROPHENYL)PROPIONIC ACID

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3-(3-CHLOROPHENYL)PROPIONIC ACID Basic information

Product Name:
3-(3-CHLOROPHENYL)PROPIONIC ACID
Synonyms:
  • Benzenepropanoic acid, 3-?chloro-
  • ASINEX-REAG BAS 10861260
  • 3-(3-CHLOROPHENYL)PROPANOIC ACID
  • 3-(3-CHLOROPHENYL)PROPIONIC ACID
  • TIMTEC-BB SBB005906
  • 3-(3-Chlorophenyl)propionic acid ,98%
  • 3-Chlorophenyl-3-propanoic acid
  • 3-Chlorobenzenepropanoic acid
CAS:
21640-48-2
MF:
C9H9ClO2
MW:
184.62
EINECS:
626-900-9
Product Categories:
  • Building Blocks
  • Carbonyl Compounds
  • Carboxylic Acids
  • Chemical Synthesis
  • Organic Building Blocks
  • Pyridines ,Halogenated Heterocycles ,Heterocyclic Acids
  • Aromatic Propionic Acids
  • C9
  • Carbonyl Compounds
  • Carboxylic Acids
Mol File:
21640-48-2.mol
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3-(3-CHLOROPHENYL)PROPIONIC ACID Chemical Properties

Melting point:
72-76 °C (lit.)
Boiling point:
263.86°C (rough estimate)
Density 
1.1989 (rough estimate)
refractive index 
1.5242 (estimate)
storage temp. 
Sealed in dry,Room Temperature
form 
solid
pka
4.59(at 25℃)
Appearance
White to off-white Solid
CAS DataBase Reference
21640-48-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
22-41-43
Safety Statements 
26-39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29163990
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3-(3-CHLOROPHENYL)PROPIONIC ACID Usage And Synthesis

Chemical Properties

White to brown powder

Synthesis

7116-35-0

21640-48-2

B. The reaction solution from step A was transferred to a 2L four-necked flask and 60.0 g of sodium hydroxide solid was added and stirred thoroughly until completely dissolved. Subsequently, the reaction mixture was slowly heated to 60-65°C and maintained at this temperature for about 3 hours. The reaction progress was monitored by gas chromatography (GC), and after confirming that the reaction endpoint was reached, the reaction solution was cooled to 20 °C. After standing and layering, the aqueous phase was separated and slowly added to 190.1 g of 30% aqueous hydrochloric acid and the pH was adjusted to about 3.0. The organic phase was collected by standing and layering again. The organic phase was dried over anhydrous sodium sulfate to give 143.2 g of the target product 3-(3-chlorophenyl)propionic acid in 77.6% yield.

References

[1] Patent: CN108329197, 2018, A. Location in patent: Paragraph 0107; 0110

3-(3-CHLOROPHENYL)PROPIONIC ACID Preparation Products And Raw materials

Raw materials

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