Welcome to LookChem.com Sign In|Join Free
  • or
5,6,7,8-Tetrahydroquinoxaline-2,3-dicarbonitrile is a heterocyclic compound with the molecular formula C8H8N4. It is a derivative of quinoxaline, a fused bicyclic aromatic compound consisting of a pyrazine ring fused to a benzene ring. The tetrahydro prefix indicates that the compound has undergone hydrogenation, reducing the degree of unsaturation in the molecule. The presence of two carbonitrile groups (-CN) at the 2 and 3 positions further characterizes 5,6,7,8-tetrahydroquinoxaline-2,3-dicarbonitrile, which is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity.

52197-14-5

Post Buying Request

52197-14-5 Suppliers

Recommended suppliers

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

52197-14-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52197-14-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,9 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52197-14:
(7*5)+(6*2)+(5*1)+(4*9)+(3*7)+(2*1)+(1*4)=115
115 % 10 = 5
So 52197-14-5 is a valid CAS Registry Number.

52197-14-5SDS

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 5,6,7,8-tetrahydroquinoxaline-2,3-dicarbonitrile

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:52197-14-5 SDS

52197-14-5Downstream Products

52197-14-5Relevant academic research and scientific papers

The symmetrical porphyrazine with annulated six membered rings

Onay, Hilal,Esat, Burak,?ztürk, Ramazan

, p. 1314 - 1316 (2010)

Tetrakis(cyclohexylpyrazino)porphyrazinato magnesium(II) with annulated six membered rings has been prepared by two different methods. In Method A: cyclotetramerization of 2,3-dicyano-5,6-cyclohexanopyrazine (1) in the presence of Mg(OPr)2 in n-propanol afforded the tetrakis(cyclohexylpyrazino)porphyrazinato magnesium(II) (2). In Method B: selenodiazole rings on the periphery of tetrakis(selenodiazole)porphyrazinato magnesium(II) were opened by the action of H2S to yield the vicinal diamino functionalities. The ring closure of the vicinal diamino groups with 1,2-cyclohexanedione afforded the tetrakis(cyclohexylpyrazino) porphyrazinato magnesium(II) (2).

A new facile, efficient synthesis and structure peculiarity of quinoxaline derivatives with two benzimidazole fragments

Mamedov, Vakhid A.,Zhukova, Nataliya A.,Syakaev, Victor V.,Gubaidullin, Aidar T.,Beschastnova, Tat'Yana N.,Adgamova, Dil'Bar I.,Samigullina, Aida I.,Latypov, Shamil K.

supporting information, p. 1403 - 1416 (2013/02/23)

A highly efficient and versatile method for the synthesis of quinoxaline derivatives with two benzimidazole fragments have been developed on the basis of the ring contraction of 3-(benzimidazo-2-yl)quinoxalin-2(1H)-one with 1,2-diaminobenzene and its various types of substituted and condensed derivatives. Owing to the inter- and intramolecular processes, involving self association, proton exchange, conformational, and/or tautomeric exchanges between several forms for most of the bis-benzimidazolylquinoxalines signals of bridged and neighboring carbon atoms and the hydrogen atoms of the neighboring carbon atoms of benzimidazole fragments in the NMR spectra are broadened. The conjugation between the benzimidazole fragments and the quinoxaline core of the molecules is increased from the quinoxaline derivative (10c) to its thiadiazol[f]- (17) and pyrrolo[a]-(19) annulated derivatives, resulting in a greater planarity of the molecule as a whole.

Direct and catalytic synthesis of quinoxaline derivatives from epoxides and ene-1,2-diamines

Antoniotti, Sylvain,Du?ach, Elisabet

, p. 3971 - 3973 (2007/10/03)

We describe here a new synthesis of quinoxaline derivatives by a Bi-catalyzed oxidative coupling of epoxides and ene-1,2-diamines.

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 52197-14-5