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

76068-42-3

Post Buying Request

76068-42-3 Suppliers

Recommended suppliers

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

76068-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76068-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,6 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76068-42:
(7*7)+(6*6)+(5*0)+(4*6)+(3*8)+(2*4)+(1*2)=143
143 % 10 = 3
So 76068-42-3 is a valid CAS Registry Number.

76068-42-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenylimino-1,1,1-trifluoro-2-pentanone

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:76068-42-3 SDS

76068-42-3Downstream Products

76068-42-3Relevant academic research and scientific papers

A highly regioselective Friedl?nder reaction mediated by lanthanum chloride

Chen, Ying,Huang, Jinkun,Hwang, Tsang-Lin,Li,Cui, Sheng,Chan, Johann,Bio, Matthew

body text, p. 3237 - 3241 (2012/07/31)

A highly efficient and regioselective Friedl?nder reaction of unsymmetrical 1,3-diketones with 2-aminoaryl aldehydes (ketones) is described. The methodology leads to the synthesis of a broad scope of substituted quinolines in high yield and excellent regioselectivity.

Quinoline formation via a modified Combes reaction: Examination of kinetics, substituent effects, and mechanistic pathways

Sloop, Joseph C.

experimental part, p. 110 - 117 (2010/04/05)

A comprehensive product regioselectlvity and kinetics study of the modified Combes quinoline synthesis shown below has been undertaken: This is the first reported investigation of the Combes condensation employing 19F NMR spectroscopy to monitor intermedi

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 76068-42-3