Welcome to LookChem.com Sign In|Join Free
  • or
1-(4-METHYLPHENOXY)-2-PROPANAMINE, also known as Atomoxetine, is a chemical compound with the molecular formula C10H15NO. It is categorized as a secondary amine and is commonly used as an intermediate in the synthesis of various pharmaceuticals and organic compounds.

61711-87-3

Post Buying Request

61711-87-3 Suppliers

Recommended suppliers

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

61711-87-3 Usage

Uses

Used in Pharmaceutical Industry:
1-(4-METHYLPHENOXY)-2-PROPANAMINE is used as an intermediate for the synthesis of various pharmaceuticals and organic compounds, due to its chemical properties and reactivity.
Used in ADHD Treatment:
1-(4-METHYLPHENOXY)-2-PROPANAMINE is used as a selective norepinephrine reuptake inhibitor for the treatment of attention deficit hyperactivity disorder (ADHD), as it helps to increase the levels of norepinephrine in the brain, improving focus and reducing impulsivity.
Used in Depression and Anxiety Treatment Research:
1-(4-METHYLPHENOXY)-2-PROPANAMINE is being studied for its potential applications in the treatment of depression and anxiety disorders, due to its effects on neurotransmitter levels and its potential to modulate mood and behavior.

Check Digit Verification of cas no

The CAS Registry Mumber 61711-87-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,1 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61711-87:
(7*6)+(6*1)+(5*7)+(4*1)+(3*1)+(2*8)+(1*7)=113
113 % 10 = 3
So 61711-87-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO/c1-8-3-5-10(6-4-8)12-7-9(2)11/h3-6,9H,7,11H2,1-2H3

61711-87-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methylphenoxy)propan-2-amine

1.2 Other means of identification

Product number -
Other names -

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:61711-87-3 SDS

61711-87-3Downstream Products

61711-87-3Relevant academic research and scientific papers

A (different) bright ammonia amide carbamate derivative and application thereof (by machine translation)

-

Paragraph 0071; 0072; 0073; 0086; 0087, (2017/07/14)

The invention belongs to the field of plant, relates to a general formula (I) is shown in a (different) bright ammonia amide carbamate derivatives and their pharmaceutically acceptable salt, wherein substituent R has the definition given in the specification, the invention also relates to the general formula (I) preparation of compounds of the, specifically for the preparation of the intermediate of its development and application of plant disease control. (by machine translation)

Design, synthesis and effect of the introduction of a propargyloxy group on the fungicidal activities of 1-substituted phenoxypropan-2-amino valinamide carbamate derivatives

Li, Jian-Qiang,Wang, Zhi-Peng,Gao, Yang,Zhao, Wei-Guang

, p. 82131 - 82137 (2016/09/09)

The cell walls of oomycetes are composed of cellulose, making cellulose synthase enzymes good targets for carboxylic acid amide fungicides. Valinamide carbamates are amino acid fungicides that represent excellent alternatives to conventional synthetic pesticides in terms of their ability to reduce the negative impacts of these compounds on human health and the environment. In a continuation of our research towards the development of new cellulose synthase inhibitors, we have developed a series of "stretched" analogues of iprovalicarb by the introduction of an additional OCH2 linker. The bioassay results indicated that compounds containing a small group at the para-position of phenyl gave excellent fungicidal activities with EC50 values ranging from 0.59 to 2.06 μmol L-1. Most notably, the introduction of a propargyloxy group led to a pronounced increase in the fungicidal activity. Furthermore, compound 7o bearing a propargyloxy group was identified as the most promising candidate because of its excellent fungicidal potency against oomycete diseases and good fungicidal activity against non-oomycete diseases.

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 61711-87-3