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6-[(2-aminoethyl)amino]-1,2,3,4-tetrahydronaphtho[2,3-f]quinoxaline-7,12-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16013-92-6

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16013-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16013-92-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,1 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16013-92:
(7*1)+(6*6)+(5*0)+(4*1)+(3*3)+(2*9)+(1*2)=76
76 % 10 = 6
So 16013-92-6 is a valid CAS Registry Number.

16013-92-6SDS

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 6-(2-aminoethylamino)-1,2,3,4-tetrahydronaphtho[3,2-f]quinoxaline-7,12-dione

1.2 Other means of identification

Product number -
Other names 6-(2-aminoethylamino)-1,2,3,4-tetrahydronaphtho<2,3-f>quinoxaline-7,12-dione

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:16013-92-6 SDS

16013-92-6Downstream Products

16013-92-6Relevant academic research and scientific papers

Antineoplastic anthraquinones. II [1]. Design and synthesis of 1,2-heteroannelated anthraquinones

Chang, Pong,Chen, Chia-Fu

, p. 367 - 371 (1996)

Based on the "2-phenyinaphthalene-type" structural pattern hypothesis, a number of heterocycle-fused anthraquinones were designed by taking morindaparvin-A (2a) as the lead structure. The compounds we synthesized and tested for antineoplastic activity include 1,2-alkylenedioxyanthraquinone, naphtho [2,3-f]-quinoxaline-7,12-dione, anthra[1,2-d]imidazole-6,11-dione and naphtho[2,3-f]quinoxaline-7,12-dione derivatives. Most of the synthesized anthraquinones possessed various degrees of anticancer activity. One of these compounds, 2-chloromethyl-1H-anthra[1,2-d]imidazole-6,11-dione (4b), exhibited cytotoxic activity against all tested human carcinoma cell lines.

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