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14923-84-3

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14923-84-3 Usage

Description

1,6-DIAMINOPYRENE, also known as 1,6-Pyrenediamine, is an organic compound that serves as an intermediate in the synthesis of various compounds. It is known for its potential carcinogenic and mutagenic properties, making it a compound of interest in the field of environmental and health sciences.

Uses

Used in Chemical Synthesis:
1,6-DIAMINOPYRENE is used as an intermediate in the synthesis of 1,8-Dinitropyrene (D480270), which is a major mutagen found in contaminated sediments. The compound plays a crucial role in the production of this potential human carcinogen, highlighting its importance in the chemical industry.
Used in Environmental and Health Research:
Due to its potential carcinogenic and mutagenic properties, 1,6-DIAMINOPYRENE is used in research to study the effects of environmental contaminants on human health. This application helps in understanding the risks associated with exposure to such compounds and contributes to the development of strategies for risk assessment and mitigation.
Used in Industrial Applications:
Although not explicitly mentioned in the provided materials, 1,6-DIAMINOPYRENE may also find use in various industrial applications, such as in the production of dyes, pigments, or other specialty chemicals, where its unique chemical properties can be exploited for specific purposes. However, it is essential to consider the potential health and environmental risks associated with its use in these applications.

Check Digit Verification of cas no

The CAS Registry Mumber 14923-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,2 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14923-84:
(7*1)+(6*4)+(5*9)+(4*2)+(3*3)+(2*8)+(1*4)=113
113 % 10 = 3
So 14923-84-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H12N2/c17-13-8-4-10-2-6-12-14(18)7-3-9-1-5-11(13)16(10)15(9)12/h1-8H,17-18H2

14923-84-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-Diaminopyrene

1.2 Other means of identification

Product number -
Other names 1,6-DIAMINOPYRENE

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:14923-84-3 SDS

14923-84-3Relevant articles and documents

Diaminopyrene modified reduced graphene oxide as a novel electrode material for excellent performance supercapacitors

Kang, Hongwei,Zhang, Chengpeng,Xu, Yonggui,Zhang, Weiyang,Jiao, Jianhua,Li, Zhikun,Zhu, LeiLei,Liu, Xiaoqian

, p. 1507 - 1513 (2020/01/25)

In this paper, novel reduced graphene oxide (rGO) composites (DAPrGOs) modified by diaminopyrene (DAP) were successfully synthesized via a facile solvothermal reaction method and used for supercapacitors. Compared with the pristine rGO, the DAPrGO1 electrode showed distinctly better performance (397.63 F g-1vs. 80.29 F g-1 of pristine rGO at 0.5 A g-1) with small charge transfer resistance. When a symmetric device was fabricated using DAPrGO1 as the active material, it also exhibited a high capacitance of 82.70 F g-1 at 0.5 A g-1 with an energy density of 25.84 W h kg-1 at a power density of 375 W kg-1, and even offered a high power density of 7500 W kg-1 (18.71 W h kg-1) at 10 A g-1. Moreover, the device possessed good electrochemical stability up to 20 000 cycles, implying promising applications in energy storage fields.

Preparation of Pure Isomers of Dinitropyrenes

Hashimoto, Yuichi,Shudo, Koichi

, p. 1992 - 1994 (2007/10/02)

Isomers of dinitripyrenes (1,3-, 1,6-, and 1,8-dinitripyrenes) uncontamined by the other isomers were prepared from the corresponding diaminopyrenes by oxidation, or nucleophilic substitution with nitrite after diazotization.Keywords: dinitropyrene; 1,3-dinitropyrene; 1,6-dinitropyrene; 1,8-dinitropyrene; diaminopyrene; preparation of nitroarenes.

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