Welcome to LookChem.com Sign In|Join Free
  • or
Benzenamine, 2-(1,1-diethoxy-2,2,3,3,4,4,4-heptafluorobutyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

181059-80-3

Post Buying Request

181059-80-3 Suppliers

Recommended suppliers

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

181059-80-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 181059-80-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,0,5 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 181059-80:
(8*1)+(7*8)+(6*1)+(5*0)+(4*5)+(3*9)+(2*8)+(1*0)=133
133 % 10 = 3
So 181059-80-3 is a valid CAS Registry Number.

181059-80-3SDS

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 2-(1,1-diethoxy-2,2,3,3,4,4,4-heptafluorobutyl)aniline

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:181059-80-3 SDS

181059-80-3Relevant academic research and scientific papers

Synthesis of aminophenyl and methoxyphenyl perfluoroalkyl ketones

Lee, Hyeran,Czarny, Agnieszka,Battiste, Merle A.,Strekowski, Lucjan

, p. 221 - 224 (2007/10/03)

The title compounds are obtained by direct hydrolysis of the corresponding 2/4-perfluoroalkyl-substituted anilines and anisoles by the system AcOH/HBr/H2O/Al2O3. A two-step preparation of 2/4-perfluoroacylanilines involves the treatment of the 2/4-perfluoroalkylaniline with sodium ethoxide followed by hydrolysis of the resultant diethyl acetal with hydriodic acid.

A novel synthesis of 4-perfluoroalkylquinolines and related substituted quinolines

Czarny, Agnieszka,Lee, Hyeran,Say, Martial,Strekowski, Lucjan

, p. 2089 - 2092 (2007/10/03)

In spite of inefficient hydrolysis of 1-(2-aminophenyl)-2,2,3,3,4,4,4-heptafluorobutan-1-one diethyl acetal (2), this compound undergoes readily the acid-catalyzed Friedl?nder reaction with enolizable ketones to give the corresponding quinolines (4-6). Th

Base-mediated reactions of ortho- and para-perfluoroalkylanilines

Strekowski, Lucjan,Lin, Shou-Yuan,Lee, Hyeran,Mason, J. Christian

, p. 4655 - 4658 (2007/10/03)

The title chemistry involves regioselectively a benzylic position of the perfluoroalkyl group and provides an easy access to substituted quinolines and methanes.

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 181059-80-3