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3-(4-methoxyphenoxy)propan-1-amine

Detailed Information

  • Product Name:3-(4-methoxyphenoxy)propan-1-amine
  • CasNo.:100841-00-7
  • MF:C10H15NO2
  • MW:181.235

pd_nature

  • Purity:99%
  • pd_boiling:36-37 °C
  • Packing:
  • Throughput:

Product Details;

CasNo: 100841-00-7

MF: C10H15NO2

Quality Factory Sells Top Purity 99% 3-(4-methoxyphenoxy)propan-1-amine 100841-00-7 with Safe Delivery

  • Molecular Formula:C10H15NO2
  • Molecular Weight:181.235
  • Vapor Pressure:0.000874mmHg at 25°C 
  • Melting Point:36-37 °C 
  • Boiling Point:304.4oC at 760 mmHg 
  • PKA:9.45±0.10(Predicted) 
  • Flash Point:150.4oC 
  • PSA:44.48000 
  • Density:1.04g/cm3 
  • LogP:2.12310 

3-(4-methoxyphenoxy)propan-1-amine(Cas 100841-00-7) Usage

General Description

3-(4-methoxyphenoxy)propan-1-amine, also known as 2-(4-methoxyphenoxy)propan-1-amine or PPG-14 butyl ether, is a chemical compound with the molecular formula C10H15NO2. It belongs to the class of amines and is derived from propan-1-amine. It is commonly used as an ingredient in various personal care and cosmetic products, suchagent for liquid household and personal care products, as well as an ingredient in lubricants and paints. It is also sometimes used as a fragrance ingredient in perfumes and colognes.

InChI:InChI=1/C10H15NO2/c1-12-9-3-5-10(6-4-9)13-8-2-7-11/h3-6H,2,7-8,11H2,1H3

100841-00-7 Relevant articles

Antitumour indolequinones: Synthesis and activity against human pancreatic cancer cells

Inman, Martyn,Visconti, Andrea,Yan, Chao,Siegel, David,Ross, David,Moody, Christopher J.

, p. 4848 - 4861 (2014/07/07)

An important determinant of the growth i...

Enantioselective synthesis of the PPARα agonist (R)-K-13675 via (S)-2-hydroxybutyrolactone

Yamazaki, Yukiyoshi,Araki, Takaaki,Koura, Minoru,Shibuya, Kimiyuki

, p. 1017 - 1022 (2008/12/22)

Enantioselective synthesis of enantiomer...

PROCESS FOR PRODUCTION OF OPTICALLY ACTIVE PPAR-ACTIVATING COMPOUND AND INTERMEDIATE OF THE SAME

-

, (2008/06/13)

A process for obtaining a compound (1) a...

OPTICALLY ACTIVE PPAR-ACTIVATING COMPOUND INTERMEDIATE AND METHOD FOR PRODUCING SAME

-

Page/Page column 7; 9, (2008/06/13)

The present invention provides a product...

100841-00-7 Process route

2-(4-Methoxyphenoxy)cyanoethane
63815-39-4

2-(4-Methoxyphenoxy)cyanoethane

3-(4-methoxyphenoxy)propan-1-amine
100841-00-7

3-(4-methoxyphenoxy)propan-1-amine

Conditions
Conditions Yield
With borane-THF; In tetrahydrofuran; at 65 ℃; for 5h;
90%
2-(4-Methoxyphenoxy)cyanoethane; With borane-THF; In tetrahydrofuran; at 80 ℃; for 3.16667h;
With sodium hydroxide; water; In tetrahydrofuran; at 0 - 80 ℃; for 12.4h;
79%
With sodium hydroxide; In tetrahydrofuran; toluene;
79%
2-(4-Methoxyphenoxy)cyanoethane; With borane-THF; In tetrahydrofuran; at 80 ℃; for 3.16h;
With sodium hydroxide; In tetrahydrofuran; water; at 0 - 80 ℃; for 12.25h;
79%
With borane-THF; In tetrahydrofuran;
<i>N</i>-[3-(4-methoxy-phenoxy)-propyl]-phthalimide
100840-46-8

N-[3-(4-methoxy-phenoxy)-propyl]-phthalimide

3-(4-methoxyphenoxy)propan-1-amine
100841-00-7

3-(4-methoxyphenoxy)propan-1-amine

Conditions
Conditions Yield
With methylamine; In methanol; at 20 ℃; for 4h;
58%
With hydrazine hydrate; In ethanol; Heating;

100841-00-7 Upstream products

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    N-[3-(4-methoxy-phenoxy)-propyl]-phthalimide

  • 63815-39-4
    63815-39-4

    2-(4-Methoxyphenoxy)cyanoethane

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    4-methoxy-phenol

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100841-00-7 Downstream products

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    n-butyl (R)-2-[3-[N-[3-(4-methoxyphenoxy)propyl]aminomethyl]phenoxy]butyrate

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    (2R)-2-[3-[[1,3-benzoxazol-2-yl-[3-(4-methoxyphenoxy)propyl]amino]methyl]phenoxy]butanoic acid

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    848258-31-1

    C28H30N2O6

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