58493-50-8

  • Product Name:Stearoyl Vanillylamide
  • Molecular Formula:C26H45NO3
  • Purity:99%
  • Molecular Weight:419.648
InquiryAdd to cart

Product Details;

CasNo: 58493-50-8

Molecular Formula: C26H45NO3

Export Quality Factory Supply Stearoyl Vanillylamide 58493-50-8 Efficient Shipping

  • Molecular Formula:C26H45NO3
  • Molecular Weight:419.648
  • Vapor Pressure:2.46E-14mmHg at 25°C 
  • Melting Point:94.5-95 °C 
  • Refractive Index:1.499 
  • Boiling Point:586.1 °C at 760 mmHg 
  • PKA:9.76±0.20(Predicted) 
  • Flash Point:308.3 °C 
  • PSA:62.05000 
  • Density:0.973 g/cm3 
  • LogP:8.11880 

Octadecanamide, N-((4-hydroxy-3-methoxyphenyl)methyl)-(Cas 58493-50-8) Usage

InChI:InChI=1/C26H45NO3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-26(29)27-22-23-19-20-24(28)25(21-23)30-2/h19-21,28H,3-18,22H2,1-2H3,(H,27,29)

58493-50-8 Relevant articles

Highly efficient synthesis of capsaicin analogues by condensation of vanillylamine and acyl chlorides in a biphase H2O/CHCl3 system

Wang, Bo,Yang, Fan,Shan, Yi-Fan,Qiu, Wen-Wei,Tang, Jie

supporting information; experimental part, p. 5409 - 5412 (2009/10/17)

Highly efficient synthesis of capsaicin ...

Lipophilicity of capsaicinoids and capsinoids influences the multiple activation process of rat TRPV1

Morita, Akihito,Iwasaki, Yusaku,Kobata, Kenji,Iida, Tohko,Higashi, Tomohiro,Oda, Kyoko,Suzuki, Asami,Narukawa, Masataka,Sasakuma, Shiho,Yokogoshi, Hidehiko,Yazawa, Susumu,Tominaga, Makoto,Watanabe, Tatsuo

, p. 2303 - 2310 (2007/10/03)

Analogs of capsaicin, such as capsaicino...

N-acylvanillamides: Development of an expeditious synthesis and discovery of new acyl templates for powerful activation of the vanilloid receptor

Appendino, Giovanni,Minassi, Alberto,Morello, Aniello Schiano,De Petrocellis, Luciano,Di Marzo, Vincenzo

, p. 3739 - 3745 (2007/10/03)

A simple and general synthesis of vanill...

Vanilloids. 1. Analogs of Capsaicin with Antinociceptive and Antiinflammatory Activity

Janusz, John M.,Buckwalter, Brian L.,Young, Patricia A.,LaHann, Thomas R.,Farmer, Ralph W.,et al.

, p. 2595 - 2604 (2007/10/02)

As part of a program to establish struct...

58493-50-8 Process route

vanillylamine hydrochloride
7149-10-2

vanillylamine hydrochloride

Stearoyl chloride
112-76-5

Stearoyl chloride

N-Vanillyloctadecanamide
58493-50-8

N-Vanillyloctadecanamide

Conditions
Conditions Yield
vanillylamine hydrochloride; With sodium hydrogencarbonate; In water; at 20 ℃; for 0.5h;
Stearoyl chloride; In chloroform; water; at 20 ℃; for 0.5h;
96%
With pyridine;
vanillylamine hydrochloride
7149-10-2

vanillylamine hydrochloride

stearic acid
57-11-4

stearic acid

N-Vanillyloctadecanamide
58493-50-8

N-Vanillyloctadecanamide

Conditions
Conditions Yield
With diethyl cyanophosphonate; triethylamine; In tetrahydrofuran;
76%

58493-50-8 Upstream products

  • 1196-92-5
    1196-92-5

    Vanillylamin

  • 112-76-5
    112-76-5

    Stearoyl chloride

  • 7149-10-2
    7149-10-2

    vanillylamine hydrochloride

  • 57-11-4
    57-11-4

    stearic acid

Relevant Products

Shopping Cart

Clear Inquiry