4-Methoxybenzamide

  • CAS No.: 3424-93-9
  • Purity: 99%
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Quality Manufacturer Supply High Purity 99% 4-Methoxybenzamide 3424-93-9 with Reasonable Price

  • Molecular Formula: C8H9NO2
  • Molecular Weight: 151.165
  • Appearance/Colour: White crystalline powder 
  • Vapor Pressure: 0.001mmHg at 25°C 
  • Melting Point: 164-167 °C(lit.) 
  • Refractive Index: 1.546 
  • Boiling Point: 295.803 °C at 760 mmHg 
  • PKA: 16.34±0.50(Predicted) 
  • Flash Point: 161.563 °C 
  • PSA: 52.32000 
  • Density: 1.144 g/cm3 
  • LogP: 1.49440 

4-Methoxybenzamide(Cas 3424-93-9) Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 103, p. 6514, 1981 DOI: 10.1021/ja00411a050Synthesis, p. 395, 1975 DOI: 10.1055/s-1975-23770Tetrahedron Letters, 36, p. 7427, 1995 DOI: 10.1016/0040-4039(95)80003-4

InChI:InChI=1/C8H9NO2/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3,(H2,9,10)

3424-93-9 Relevant articles

The Acid-Catalyzed and Uncatalyzed Hydrolysis of Nitriles on Unactivated Alumina

Wilgus, Catherine Pala,Downing, Susan,Molitor, Erich,Bains, Satinder,Pagni, Richard M.,Kabalka, George W.

, p. 3469 - 3472 (1995)

Nitriles are selectively converted into ...

Influence of bulky yet flexible N-heterocyclic carbene ligands in gold catalysis

Collado, Alba,Patrick, Scott R.,Gasperini, Danila,Meiries, Sebastien,Nolan, Steven P.

, p. 1809 - 1814 (2015)

Three new Au(I) complexes of the formula...

A Mild Heteroatom (O -, N -, and S -) Methylation Protocol Using Trimethyl Phosphate (TMP)-Ca(OH) 2Combination

Tang, Yu,Yu, Biao

, (2022/03/27)

A mild heteroatom methylation protocol u...

Process Development of the Copper(II)-Catalyzed Dehydration of a Chiral Aldoxime and Rational Selection of the Co-Substrate

Gr?ger, Harald,Nonnhoff, Jannis

, (2021/12/14)

The access towards chiral nitriles remai...

Visible light-mediated synthesis of amides from carboxylic acids and amine-boranes

Chen, Xuenian,Kang, Jia-Xin,Ma, Yan-Na,Miao, Yu-Qi

supporting information, p. 3595 - 3599 (2021/06/06)

Here, a photocatalytic deoxygenative ami...

Method for preparing primary and secondary amide compounds

-

Paragraph 0057-0067, (2021/02/06)

The invention belongs to the field of or...

3424-93-9 Process route

4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

4-methoxyphenylacetamide
3424-93-9

4-methoxyphenylacetamide

4-methoxybenzoic acid
100-09-4

4-methoxybenzoic acid

Conditions
Conditions Yield
With pylyphosphoric acid; hydroxylamine hydrochloride; In acetic acid; at 118 - 120 ℃; for 1.5h;
35%
40%
4-methoxybenzonitrile
874-90-8

4-methoxybenzonitrile

4-methoxyphenylacetamide
3424-93-9

4-methoxyphenylacetamide

4-methoxybenzoic acid
100-09-4

4-methoxybenzoic acid

Conditions
Conditions Yield
fluorapatite; synthetic; sodium nitrite; In water; at 100 ℃; for 24h;
60%

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    4-Methoxypropiophenone

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