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42135-22-8

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42135-22-8 Usage

Description

3-Nitrofluorenone is a nitrated polycyclic aromatic hydrocarbon (PAH) with mutagenic activity.

Uses

Used in Chemical Research:
3-Nitrofluorenone is used as a research chemical for studying its mutagenic properties and potential applications in various chemical reactions.
Used in Environmental Monitoring:
3-Nitrofluorenone is used as an indicator of environmental pollution, as it can be detected in air, water, and soil samples, providing information about the presence of PAHs and their potential health risks.
Used in Pharmaceutical Development:
3-Nitrofluorenone is used as a starting material in the synthesis of various pharmaceutical compounds, including drugs with potential therapeutic applications.
Used in Material Science:
3-Nitrofluorenone is used in the development of new materials with unique properties, such as high thermal stability and resistance to chemical degradation, for use in various industries.

Reactivity Profile

A nitrated ketone. Ketones are reactive with many acids and bases liberating heat and flammable gases (e.g., H2). The amount of heat may be sufficient to start a fire in the unreacted portion of the ketone. Ketones react with reducing agents such as hydrides, alkali metals, and nitrides to produce flammable gas (H2) and heat. Ketones are incompatible with isocyanates, aldehydes, cyanides, peroxides, and anhydrides. They react violently with aldehydes, HNO3, HNO3 + H2O2, and HClO4.

Health Hazard

ACUTE/CHRONIC HAZARDS: When heated to decomposition 3-nitrofluoren-9-one emits toxic fumes.

Fire Hazard

Flash point data for 3-nitrofluoren-9-one are not available. 3-nitrofluoren-9-one is probably combustible.

Check Digit Verification of cas no

The CAS Registry Mumber 42135-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,1,3 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 42135-22:
(7*4)+(6*2)+(5*1)+(4*3)+(3*5)+(2*2)+(1*2)=78
78 % 10 = 8
So 42135-22-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H7NO3/c15-13-10-4-2-1-3-9(10)12-7-8(14(16)17)5-6-11(12)13/h1-7H

42135-22-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Nitrofluorenone

1.2 Other means of identification

Product number -
Other names 3-nitrofluoren-9-one

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:42135-22-8 SDS

42135-22-8Relevant articles and documents

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Pan,H.-L. et al.

, p. 716 (1975)

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Palladium catalyzed domino C-H activation strategy: An access to 9- fluorenones

Patel, Anuj,Shaikh, Mahommedumar,Chikhalia, Kishor

supporting information, p. 236 - 245 (2018/12/11)

Palladium catalyzed domino C-H functionalization reaction of arylaldehyde with dihaloarene has been developed to access 9-flourenone molecules. Bidentate ligand assisted strategy, single step reaction, high yield and excellent functional group tolerance make this method concise and effective for the synthesis of 9-flourenone. In addition, proposed method has been successfully employed to synthesise Tilorone in gram scale.

Metallocene compounds, and preparation and use thereof for synthesis of poly-alpha-olefins as lubricating base oil

-

Paragraph 0058; 0059, (2018/10/04)

The present invention relates to a metallocene compound, and preparation and use thereof, and the compound can be used as a catalyst for synthesis of poly-α-olefin as lubricating base oil. The metallocene compound includes a substituted aryl group, a bridged atom, an optionally unsubstituted, 3-mono-substituted or 3,6-disubstituted 5H-indeno [1,2-b] pyridyl group or optionally unsubstituted, 3-mono-substituted or 3,6-disubstituted 5H-indeno [1,2-b] thiopyranyl group, and a metal coordination group. As a catalyst, the metallocene compound is shown to be structurally stable and high in catalytic efficiency, and the preparation of the catalyst is relatively easy in operation, high in yield, low in cost, low in pollution and easy to scale up for industrial production.

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