16603-18-2

  • Product Name:3,4,5-TRIMETHOXYPHENYLACETONE
  • Molecular Formula:C12H16 O4
  • Molecular Weight:224.257
Inquiry

Product Details

pd_meltingpoint:58-62°C

Purity:99%

Manufacturer supply top purity 3,4,5-TRIMETHOXYPHENYLACETONE 16603-18-2 with GMP standards

  • Molecular Formula:C12H16 O4
  • Molecular Weight:224.257
  • Vapor Pressure:0.000451mmHg at 25°C 
  • Melting Point:58-62°C 
  • Boiling Point:314.9°Cat760mmHg 
  • Flash Point:136.1°C 
  • PSA:44.76000 
  • Density:1.078g/cm3 
  • LogP:1.84390 

3,4,5-TRIMETHOXYPHENYLACETONE(Cas 16603-18-2) Usage

General Description

3,4,5-Trimethoxyphenylacetone is a chemical compound with a molecular formula of C12H16O4. It is a phenylacetone derivative and is also known by the chemical name "Vanillin Acetate". 3,4,5-TRIMETHOXYPHENYLACETONE is a clear, colorless to yellowish liquid with a sweet, floral odor. It is commonly used as a flavoring agent in the food industry, particularly in the production of vanilla flavoring. Additionally, 3,4,5-trimethoxyphenylacetone has been studied for its potential antimicrobial and antioxidant properties. 3,4,5-TRIMETHOXYPHENYLACETONE is also used in the synthesis of various pharmaceuticals and other organic compounds.

InChI:InChI=1/C12H16O4/c1-8(13)5-9-6-10(14-2)12(16-4)11(7-9)15-3/h6-7H,5H2,1-4H3

16603-18-2 Relevant articles

A convenient and efficient one-pot synthesis of arylacetones from (E)-3-aryl-2-methylacrylic acids by curtius rearrangement

He, Xin,Cao, Chong,Liang, Jingwei,Li, Xinyang,Zhang, Tingjian,Meng, Fanhao

, p. 386 - 390 (2017/02/10)

A convenient and efficient method was de...

Iron-Mediated One-Pot Synthesis of 3,5-Diarylpyridines from β-Nitrostyrenes

Sathish, Manda,Chetna, Jadala,Hari Krishna, Namballa,Shankaraiah, Nagula,Alarifi, Abdullah,Kamal, Ahmed

, p. 2159 - 2165 (2016/03/15)

An operationally simple and mild one-pot...

Addressing challenges in palladium-catalyzed cross-couplings of aryl mesylates: Monoarylation of ketones and primary alkyl amines

Alsabeh, Pamela G.,Stradiotto, Mark

supporting information, p. 7242 - 7246 (2013/07/26)

Mor(DalPhos) for Me(sylates): Described ...

Palladium-catalyzed mono-α-arylation of acetone with aryl imidazolylsulfonates

Ackermann, Lutz,Mehta, Vaibhav P.

supporting information; experimental part, p. 10230 - 10233 (2012/09/22)

Set the ace(tone): A palladium catalyst ...

16603-18-2 Process route

1-(3,4,5-trimethoxyphenyl)-2-nitro-1-propene
5556-76-3

1-(3,4,5-trimethoxyphenyl)-2-nitro-1-propene

(3,4,5-trimethoxyphenyl)acetone
16603-18-2

(3,4,5-trimethoxyphenyl)acetone

Conditions
Conditions Yield
With hydrogen; acetic acid; nickel; at 25 ℃; for 15h;
65%
With hydrogenchloride; iron(III) chloride; iron;
With hydrogenchloride; iron(III) chloride; iron; In toluene; Heating;
(E)-1,2,3-trimethoxy-5-(2-nitroprop-1-enyl)benzene
38059-94-8

(E)-1,2,3-trimethoxy-5-(2-nitroprop-1-enyl)benzene

(3,4,5-trimethoxyphenyl)acetone
16603-18-2

(3,4,5-trimethoxyphenyl)acetone

Conditions
Conditions Yield
With iron; In acetic acid; at 20 ℃; for 0.5h;
94%

16603-18-2 Upstream products

  • 5556-76-3
    5556-76-3

    1-(3,4,5-trimethoxyphenyl)-2-nitro-1-propene

  • 317806-14-7
    317806-14-7

    1,2,3-trimethoxy-5-(2-nitro-propenyl)benzene

  • 107951-83-7
    107951-83-7

    1,2,3-Trimethoxy-5-[2-methylsulfanyl-2-(toluene-4-sulfonyl)-propyl]-benzene

  • 19037-58-2
    19037-58-2

    1-(3,5-dimethoxy-4-hydroxyphenyl)propan-2-one

16603-18-2 Downstream products

  • 136178-78-4
    136178-78-4

    2-(3,4,5-trimethoxybenzyl)-2,3-dimethyloxazolidine

  • 136178-71-7
    136178-71-7

    2,2-dimethoxy-1-(3,4,5-trimethoxyphenyl)propane

  • 157024-69-6
    157024-69-6

    2-isopropylcarbonyloxy-4-(3-methoxy-4,5-methylenedioxyphenyl)-2-methyl-1-(3,4,5-trimethoxyphenyl)butane

  • 50544-08-6
    50544-08-6

    5,5'-(2,3-dimethylbutane-1,4-diyl)bis(1,2,3-trimethoxybenzene)

Relevant Products