Welcome to LookChem.com Sign In|Join Free

CAS

  • or

39065-95-7

Post Buying Request

39065-95-7 Suppliers

Recommended suppliersmore

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

39065-95-7 Usage

Description

4-(Chloro-difluoro-methoxy)-phenylamine is an organic compound characterized by its chloro-difluoro-methoxy group attached to a phenylamine backbone. This molecule exhibits unique chemical properties due to the presence of the halogenated and fluorinated functional groups, which may contribute to its reactivity and potential applications in various chemical and pharmaceutical processes.

Uses

Used in Pharmaceutical Industry:
4-(Chloro-difluoro-methoxy)-phenylamine is used as a reactant for the preparation of arylphthalazines, which are potent and orally bioavailable inhibitors of VEGFR-2 (Vascular Endothelial Growth Factor Receptor-2). These inhibitors play a crucial role in the development and progression of various cancers by targeting the angiogenesis process, which is essential for tumor growth and metastasis. The unique structural features of 4-(Chloro-difluoro-methoxy)-phenylamine contribute to the enhanced efficacy and selectivity of the resulting arylphthalazine inhibitors.

Check Digit Verification of cas no

The CAS Registry Mumber 39065-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,6 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 39065-95:
(7*3)+(6*9)+(5*0)+(4*6)+(3*5)+(2*9)+(1*5)=137
137 % 10 = 7
So 39065-95-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClF2NO/c8-7(9,10)12-6-3-1-5(11)2-4-6/h1-4H,11H2

39065-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[chloro(difluoro)methoxy]aniline

1.2 Other means of identification

Product number -
Other names 4-Chlorodifluoromethoxyaniline

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:39065-95-7 SDS

39065-95-7Relevant articles and documents

Synergistic effects in Fe nanoparticles doped with ppm levels of (Pd + Ni). A new catalyst for sustainable nitro group reductions

Pang, Haobo,Gallou, Fabrice,Sohn, Hyuntae,Camacho-Bunquin, Jeffrey,Delferro, Massimiliano,Lipshutz, Bruce H.

supporting information, p. 130 - 135 (2018/01/12)

A remarkable synergistic effect has been uncovered between ppm levels of Pd and Ni embedded within iron nanoparticles that leads to mild and selective catalytic reductions of nitro-containing aromatics and heteroaromatics in water at room temperature. NaBH4 serves as the source of inexpensive hydride. Broad substrate scope is documented, along with several other features including: low catalyst loading, low residual metal in the products, and recycling of the catalyst and reaction medium, highlight the green nature of this new technology.

Hydrogenation on granular palladium-containing catalysts: II. Hydrogenation of nitroheterocyclic compounds

Kislyi,Tolkacheva,Semenov

, p. 269 - 271 (2007/10/03)

Nitroheterocyclic compounds were reduced in a classical reactor with an agitator equipped with a cell for fixed bed of catalyst. As catalysts were applied granular palladium catalysts (0.5% of Pd on γ-Al2O 3 and 2% of Pd on granulated carbon). Anilines and 3-amino-2(1H)-pyridones were obtained in high yield at reduction of the appropriate nitro compounds, and the activity of the catalyst samples only slightly decreased. Yet aminopyrazoles and aminoimidazoles obtained by hydrogenation on palladium were very sensitive to the presence of air even as hydrochlorides. In the course of hydrogenation of nitropyrazoles and nitroimidazoles the activity of the catalyst markedly decreased.

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

What can I do for you?
Get Best Price

Get Best Price for 39065-95-7