Welcome to LookChem.com Sign In|Join Free

CAS

  • or

716-81-4

Post Buying Request

716-81-4 Suppliers

Recommended suppliersmore

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

716-81-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 716-81-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 716-81:
(5*7)+(4*1)+(3*6)+(2*8)+(1*1)=74
74 % 10 = 4
So 716-81-4 is a valid CAS Registry Number.

716-81-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-(trifluoromethyl)-3,4-dihydro-1H-quinoxalin-2-one

1.2 Other means of identification

Product number -
Other names 3,4-dihydro-7-trifluoromethyl-2(1H)-quinoxalinone

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:716-81-4 SDS

716-81-4Downstream Products

716-81-4Relevant articles and documents

Solid-phase traceless synthesis of selected nitrogen-containing heterocyclic compounds. The encore technique for directed sorting of modular solid support

Krchnak, Viktor,Smith, Jennifer,Vagner, Josef

, p. 1078 - 1106 (2001)

The acid lability of electron-rich N-benzylanilines has been exploited in a linker for the traceless solid-phase synthesis of benzimidazoles, 2-aminobenzimidazoles, quinoxalinones and tetrahydroquinoxalines. The target compound precursors were assembled o

A Combination of Visible-Light Organophotoredox Catalysis and Asymmetric Organocatalysis for the Enantioselective Mannich Reaction of Dihydroquinoxalinones with Ketones

Rostoll-Berenguer, Jaume,Blay, Gonzalo,Mu?oz, M. Carmen,Pedro, José R.,Vila, Carlos

supporting information, p. 6011 - 6015 (2019/08/26)

An enantioselective photooxidative Mannich reaction of dihydroquinoxalinones with ketones by the merger of organophotoredox and asymmetric organocatalysis is described. This protocol features very mild reaction conditions using simple and cheap catalysts (Eosin Y and (S)-Proline) for the synthesis of chiral quinoxaline derivatives with good to high yields (up to 94%) and excellent enantioselectivities (up to 99% ee).

Quinoxaline compounds as hypnotic agents

-

, (2008/06/13)

The present invention is concerned with the use of certain quinoxaline compounds as hypnotic agents.

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 716-81-4