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1-Bromonaphthalen-2-yl 2,3-diphenylquinoxaline-6-carboxylate is a complex organic compound with the molecular formula C31H20BrN2O2. It is characterized by a naphthalene ring substituted with a bromine atom at the 1-position, and a quinoxaline ring with a carboxylate group at the 6-position. The quinoxaline ring is further adorned with two phenyl groups at the 2 and 3 positions. 1-bromonaphthalen-2-yl 2,3-diphenylquinoxaline-6-carboxylate is of interest in the field of organic chemistry and materials science, potentially for its electronic properties or as a building block in the synthesis of more complex molecules. It is likely to be used in research settings to explore its chemical reactivity, stability, and possible applications in areas such as pharmaceuticals or advanced materials.

7047-14-5

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7047-14-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7047-14-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,4 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7047-14:
(6*7)+(5*0)+(4*4)+(3*7)+(2*1)+(1*4)=85
85 % 10 = 5
So 7047-14-5 is a valid CAS Registry Number.

7047-14-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-bromonaphthalen-2-yl) 2,3-diphenylquinoxaline-6-carboxylate

1.2 Other means of identification

Product number -
Other names 5-<4-Nitro-phenyl>-1.2.4-dithiazolon-3

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:7047-14-5 SDS

7047-14-5Relevant academic research and scientific papers

Thioacyl Isocyanates, XII. Preparation and Comparison of Aliphatic, Aromatic, and Heteroaromatic Compounds

Goerdeler, Joachim,Nandi, Kumaresh

, p. 549 - 563 (2007/10/02)

Many 1,2,4-dithiazol-3-ones (2), especially with aliphatic and heterocyclic substituents, and some thiazoline-4,5-diones (3) were synthesized from thioamides (1).Extrusion of sulfur or carbon monoxide, respectively, afforded the thioacyl isocyanates 5.Rea

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