111128-12-2

  • Product Name:4-Bromomethylphenylacetic Acid
  • Molecular Formula:C10H11BrO2
  • Purity:99%
  • Molecular Weight:243.1
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Product Details;

CasNo: 111128-12-2

Molecular Formula: C10H11BrO2

Appearance: Beige-cream crystalline powder

Buy reliable Quality 4-Bromomethylphenylacetic Acid 111128-12-2 raw material with Honest Price

  • Molecular Formula:C10H11BrO2
  • Molecular Weight:243.1
  • Appearance/Colour:Beige-cream crystalline powder 
  • Vapor Pressure:2.54E-05mmHg at 25°C 
  • Melting Point:126-130 °C(lit.) 
  • Refractive Index:1.5220 (estimate) 
  • Boiling Point:344.2 °C at 760 mmHg 
  • PKA:4.29±0.10(Predicted) 
  • Flash Point:162 °C 
  • PSA:37.30000 
  • Density:1.485 g/cm3 
  • LogP:2.76960 

2-(4-Bromomethyl)phenylpropionic acid(Cas 111128-12-2) Usage

General Description

2-[4-(Bromomethyl)phenyl]propionic acid is a propionic acid derivative. Its enthalpy of vaporization at boiling point (421.15K) is 36.363kjoule/mol and density at 25°C is 1.4212g/ml.

InChI:InChI=1/C10H11BrO2/c1-7(10(12)13)9-4-2-8(6-11)3-5-9/h2-5,7H,6H2,1H3,(H,12,13)/p-1/t7-/m1/s1

111128-12-2 Relevant articles

Design, synthesis, and evaluation of novel 2-phenylpropionic acid derivatives as dual COX inhibitory-antibacterial agents

Karaca Gen?er, Hülya,Acar ?evik, Ulviye,Kaya ?avu?o?lu, Betül,Sa?l?k, Begüm Nurpelin,Levent, Serkan,Atl?, ?zlem,Ilg?n, Sinem,?zkay, Yusuf,Kaplanc?kl?, Zafer As?m

, p. 732 - 745 (2017)

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Method for synthesizing P-bromomethyl isobenzopropionic acid

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, (2021/10/27)

The invention provides a method for synt...

Preparation method of p-bromomethyl isophenylpropionic acid

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Paragraph 0014; 0015; 0044; 0049; 0050; 0051; 0056; 0057, (2020/08/09)

The invention belongs to the field of sy...

Production method of 2-(4-bromomethyl phenyl)propionic acid

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Paragraph 0017; 0022; 0028; 0029, (2020/03/06)

The invention discloses a production met...

Liquid-phase circulation preparation method for 2-(4-bromomethylphenyl)propionic acid

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Paragraph 0063-0075; 0077; 0089-0095; 0097-0099; 0101-0103, (2019/01/22)

The invention discloses a liquid-phase c...

111128-12-2 Process route

formaldehyd
50-00-0,30525-89-4,61233-19-0

formaldehyd

hydratropic acid
492-37-5,2328-24-7

hydratropic acid

2-[4-(bromomethyl)phenyl]propanoic acid
111128-12-2

2-[4-(bromomethyl)phenyl]propanoic acid

Conditions
Conditions Yield
With sulfuric acid; hydrogen bromide; at 35 - 70 ℃; for 11h; Temperature;
99%
With sulfuric acid; hydrogen bromide; at 35 - 90 ℃; for 11.5h; Temperature;
96%
formaldehyd; hydratropic acid; With hydrogen bromide; at 55 - 65 ℃;
With sulfuric acid; at 20 - 65 ℃;
96%
With 1-dodecyl-3-methylimidazol-1-ium bromide; hydrogen bromide; In water; at 60 ℃; for 6h; Reagent/catalyst;
87%
With hydrogen bromide; phosphorus tribromide; zinc dibromide; In n-heptane; water; at 80 - 90 ℃; for 14h;
86%
With hydrogen bromide; phosphorus tribromide; zinc dibromide; In water; at 80 - 90 ℃; for 10h; Concentration; Reagent/catalyst; Temperature; Time;
86.7%
With sulfuric acid; hydrogen bromide; at 50 - 120 ℃; for 3h; Time; Temperature;
80.8%
C<sub>10</sub>H<sub>10</sub>Br<sub>2</sub>O<sub>2</sub>

C10H10Br2O2

2-[4-(bromomethyl)phenyl]propanoic acid
111128-12-2

2-[4-(bromomethyl)phenyl]propanoic acid

Conditions
Conditions Yield
With tetra-(n-butyl)ammonium iodide; phosphonic acid diethyl ester; In water; toluene; at 5 - 85 ℃; for 6h; Reagent/catalyst; Inert atmosphere;
85.3%

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    formaldehyd

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