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207-11-4

207-11-4

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207-11-4 Usage

Chemical Properties

beige to light brown powder

Check Digit Verification of cas no

The CAS Registry Mumber 207-11-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,0 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 207-11:
(5*2)+(4*0)+(3*7)+(2*1)+(1*1)=34
34 % 10 = 4
So 207-11-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H10N2/c1-2-10-15-14(9-1)19-17-12-7-3-5-11-6-4-8-13(16(11)12)18(17)20-15/h1-10H

207-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ACENAPHTHO(1,2-B)QUINOXALINE

1.2 Other means of identification

Product number -
Other names 7,12-diazabenzo<k>fluoranthen

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:207-11-4 SDS

207-11-4Related news

Acenaphtho[1,2-b]quinoxaline diimides derivative as a potential small molecule non-fullerene acceptor for organic solar cells09/30/2019

We designed and synthesized a small molecule acenaphtho[1,2-b]quinoxaline diimide derivative AQI-T2 as an electron-accepting material for non-fullerene organic solar cells. This molecule exhibits a relatively broad absorption band from 300 to 650 nm, with a moderately low-lying lowest unoccupied...detailed

Novel conjugated polymers with planar backbone bearing acenaphtho[1,2-b]quinoxaline acceptor subunit for polymer solar cells09/29/2019

Dialkoxy substituted acenaphtho [1,2-b]quinoxaline (AQx) is demonstrated to be a promising electronic acceptor subunit for constructing high performance donor-acceptor (D–A) photovoltaic copolymers. Using it as acceptor and benzo[1,2-b:4,5-b′]-dithiophene (BDT) or thiophene (T) as donor units,...detailed

Acenaphtho[1,2-b]quinoxaline and acenaphtho[1,2-b]pyrazine as corrosion inhibitors for mild steel in acid medium09/28/2019

The corrosion inhibition of mild steel in 1M H2SO4 using acenaphtho[1,2-b]quinoxaline and acenaphtho[1,2-b]pyrazine at 303–333K have been investigated. The study was performed using weight loss method, potentiodynamic polarization, and electrochemical impedance spectroscopy (EIS). Polarization ...detailed

207-11-4Relevant articles and documents

Condensation of 1-(dicyanomethylene)acenaphthene-2-one with aromatic diamines

El-Shaieb, Kamal M.

experimental part, p. 1150 - 1155 (2009/12/04)

1-(Dicyanomethylene)acenaphthene-2-one (1) reacts with 1,8- diaminonaphthalene (2) to yield two products, identified as acenaphtho[1,2-b] naphtho[1,8-ef][1,4]diazepine (3) and (Z)-2-(8-aminonaphthalen-1-ylamino)-2-(2- oxoacenaphthylen-1(2H)-ylidene)aceton

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