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136773-69-8

136773-69-8

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136773-69-8 Usage

Chemical Properties

Crystalline Solid

Uses

4-Chloro-7-fluoropyrrolo[1,2-a]quinoxaline (cas# 136773-69-8) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 136773-69-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,7,7 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 136773-69:
(8*1)+(7*3)+(6*6)+(5*7)+(4*7)+(3*3)+(2*6)+(1*9)=158
158 % 10 = 8
So 136773-69-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H6ClFN2/c12-11-10-2-1-5-15(10)9-4-3-7(13)6-8(9)14-11/h1-6H

136773-69-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-CHLORO-7-FLUOROPYRROLO[1,2-A]QUINOXALINE

1.2 Other means of identification

Product number -
Other names Pyrrolo[1,2-a]quinoxaline,4-chloro-7-fluoro

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:136773-69-8 SDS

136773-69-8Relevant articles and documents

Pyrroloquinoxaline hydrazones as fluorescent probes for amyloid fibrils

Gemma, Sandra,Colombo, Laura,Forloni, Gianluigi,Savini, Luisa,Fracasso, Claudia,Caccia, Silvio,Salmona, Mario,Brindisi, Margherita,Joshi, Bhupendra P.,Tripaldi, Pierangela,Giorgi, Gianluca,Taglialatela-Scafati, Orazio,Novellino, Ettore,Fiorini, Isabella,Campiani, Giuseppe,Butini, Stefania

scheme or table, p. 5137 - 5148 (2011/09/14)

Here we describe the identification and preliminary characterization of a new class of pyrrolo(imidazo)quinoxaline hydrazones as flurescent probes for Aβ1-42 fibrils. All the newly developed compounds were able to bind amyloid fibrils formed in

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