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alpha-Methylcinnamic acid

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alpha-Methylcinnamic acid manufacturers

alpha-Methylcinnamic acid Basic information
Product Name:alpha-Methylcinnamic acid
Synonyms:2-Methyl-3-phenyl-2-propenoic acid;alpha-Methylcinnamic acid,99%;α-Methylciamic acid;2M3B;alpha-Methylcinnamic acid 99%;(2E)-2-methyl-3-phenylacrylic acid;RARECHEM AL BM 0531;(2E)-2-Methyl-3-phenyl-2-propenoic acid
CAS:1199-77-5
MF:C10H10O2
MW:162.19
EINECS:214-847-0
Product Categories:Building Blocks;Carbonyl Compounds;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks;Carboxylic Acids;C10;Carbonyl Compounds;Cinnamic acid;1199-77-5;11
Mol File:1199-77-5.mol
alpha-Methylcinnamic acid Structure
alpha-Methylcinnamic acid Chemical Properties
Melting point 79-81 °C(lit.)
Boiling point 288 °C
density 1.0281 (rough estimate)
refractive index 1.6000 (estimate)
storage temp. Sealed in dry,Room Temperature
form Crystals or Crystalline Powder
pka4.82±0.10(Predicted)
color White to yellow
BRN 2042544
InChIInChI=1S/C10H10O2/c1-8(10(11)12)7-9-5-3-2-4-6-9/h2-7H,1H3,(H,11,12)
InChIKeyXNCRUNXWPDJHGV-BQYQJAHWSA-N
SMILESC(O)(=O)C(C)=CC1=CC=CC=C1
LogP2.600
CAS DataBase Reference1199-77-5(CAS DataBase Reference)
NIST Chemistry Reference«ALPHA»-methylcinnamic acid(1199-77-5)
Safety Information
Safety Statements 22-24/25
WGK Germany 3
HS Code 29163900
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
alpha-Methylcinnamic acid English
ACROS English
SigmaAldrich English
ALFA English
alpha-Methylcinnamic acid Usage And Synthesis
Chemical PropertiesWHITE TO YELLOWISH CRYSTALS OR CRYSTALLINE POWDER
UsesAlpha-methylcinnamic acid
Synthesis Reference(s)Journal of the American Chemical Society, 94, p. 2520, 1972 DOI: 10.1021/ja00762a060
Synthetic Communications, 19, p. 71, 1989 DOI: 10.1080/00397918908050954
Synthesis
Benzaldehyde

100-52-7

Propionic anhydride

123-62-6

alpha-Methylcinnamic acid

1199-77-5

General procedure: Propionic anhydride (300 mmol, 1.6 eq.) was slowly added to a reaction vial containing potassium carbonate (224 mmol, 1.2 eq.) at 0 °C. After stirring for 5 min, benzaldehyde (186 mmol, 1.0 eq.) was added dropwise to the mixture. The reaction mixture was heated to reflux and maintained for 12 hours. Upon completion of the reaction, the mixture was cooled to room temperature using an ice bath, followed by addition of water (appropriate amount) and solid Na2CO3 (30 g) to the reaction mixture. The resulting yellow precipitate was collected by filtration and the filtrate was acidified to pH 6.0 with concentrated HCl to precipitate a solid product of 2-methyl-3-phenylpropenoic acid.

References[1] Medicinal Chemistry Research, 2004, vol. 13, # 8-9, p. 660 - 676
[2] European Journal of Medicinal Chemistry, 2013, vol. 62, p. 632 - 648
[3] American Chemical Journal, 1906, vol. 36, p. 533
[4] Journal of the Chemical Society, 1877, vol. 31, p. 409
[5] Journal of the Chemical Society, 1878, vol. 33, p. 215
alpha-Methylcinnamic acid Preparation Products And Raw materials
Raw materialsBenzaldehyde-->Iodobenzene-->Bromobenzene-->Methacrylic acid-->Propionic anhydride
Preparation ProductsBMK methyl glycidate
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