Welcome to LookChem.com Sign In|Join Free
  • or
1-Amino-4-(4-methylphenoxy)butane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75716-46-0

Post Buying Request

75716-46-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

75716-46-0 Usage

Structure

Butane backbone with an amino group (-NH2) and a 4-methylphenoxy substituent (-OC6H4-CH3)

Classification

Amine derivative

Usage

Commonly used in the synthesis of pharmaceutical compounds and as an intermediate in organic synthesis

Potential

Can be used in medicinal chemistry for the development of novel drugs due to its structural properties and potential pharmacological activity

Safety considerations

Handle with care, as it may have specific hazards associated with it.

Check Digit Verification of cas no

The CAS Registry Mumber 75716-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,1 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75716-46:
(7*7)+(6*5)+(5*7)+(4*1)+(3*6)+(2*4)+(1*6)=150
150 % 10 = 0
So 75716-46-0 is a valid CAS Registry Number.

75716-46-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Amino-4-(4-methylphenoxy)butane

1.2 Other means of identification

Product number -
Other names 4-p-tolyloxy-butylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:75716-46-0 SDS

75716-46-0Relevant academic research and scientific papers

N- versus O-arylation of aminoalcohols: Orthogonal selectivity in copper-based catalysts

Shafir, Alexandr,Lichtor, Phillip A.,Buchwald, Stephen L.

, p. 3490 - 3491 (2008/01/01)

Two complementary protocols for copper-catalyzed arylation of aminoalcohols were developed. Selective N-arylation was accomplished at room temperature using 2-isobutyrylcyclohexanone (a β-diketone) as supporting ligand, while selective O-arylation require

Imidazole compounds

-

, (2008/06/13)

A novel class of imidazo heterocyclic compounds, pharmaceutical compositions comprising them and use thereof in the treatment and/or prevention of diseases and disorders related to the histamine H3 receptor. More particularly, the compounds are useful for the treatment and/or prevention of diseases and disorders in which an interaction with the histamine H3 receptor is beneficial.

New, Easily Removable Poly(ethylene glycol) Supports for the Liquid-Phase Method of Peptide Synthesis

Pillai, V. N. Rajasekharan,Mutter, Manfred,Bayer, Ernst,Gatfield, Ian

, p. 5364 - 5370 (2007/10/02)

Poly(ethylene glycol) (PEG) was derivatized with a number of acid-cleavable and photocleavable anchoring groups in order to test the applicability of these derivatives as supports in liquid-phase peptide synthesis.PEG was subjected to rapid and quantitati

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 75716-46-0