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42523-38-6

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42523-38-6 Usage

General Description

7-NITRO-9-OXO-4-FLUORENECARBOXYLIC ACID is a chemical compound with the molecular formula C15H9NO5. It is a nitroaromatic compound that is commonly used in the synthesis of pharmaceuticals and agrochemicals. 7-NITRO-9-OXO-4-FLUORENECARBOXYLIC ACID is known for its high reactivity and is often used as a precursor in organic synthesis. It can also be used as a research chemical in various fields, including medicinal chemistry and pharmacology. The compound is classified as a carboxylic acid, which means it contains a carboxyl group consisting of a carbonyl group and a hydroxyl group bonded to a carbon atom. Its chemical properties make it valuable for a wide range of applications in the chemical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 42523-38-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,5,2 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 42523-38:
(7*4)+(6*2)+(5*5)+(4*2)+(3*3)+(2*3)+(1*8)=96
96 % 10 = 6
So 42523-38-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H7NO5/c16-13-9-2-1-3-10(14(17)18)12(9)8-5-4-7(15(19)20)6-11(8)13/h1-6H,(H,17,18)

42523-38-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-nitro-9-oxofluorene-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 7-Nitro-9-fluorenone-4-carboxylic acid

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:42523-38-6 SDS

42523-38-6Relevant articles and documents

Boosting the photovoltaic thermal stability of fullerene bulk heterojunction solar cells through charge transfer interactions

Yi Ho, Carr Hoi,Cao, Huanyang,Lu, Yong,Lau, Tsz-Ki,Cheung, Sin Hang,Li, Ho-Wa,Yin, Hang,Chiu, Ka Lok,Ma, Lik-Kuen,Cheng, Yuanhang,Tsang, Sai-Wing,Lu, Xinhui,So, Shu Kong,Ong, Beng S.

supporting information, p. 23662 - 23670 (2017/11/30)

Fullerene-based bulk heterojunction organic solar cells (BHJ-OSCs) represent one of the current state-of-the-art organic solar cells. Nonetheless, most of these devices still suffer from adverse performance degradation due to thermally induced morphology changes of active layers. We herein demonstrate that the photovoltaic performance stability of BHJ-OSCs can be profoundly enhanced with an appositely functionalized 9-fluorenylidene malononitrile. The latter, through charge transfer (CT) interactions with a donor polymer, enables the formation of a frozen 3-dimensional mesh-like donor polymer matrix, which effectively restrains free movement of embedded fullerene molecules and suppresses their otherwise uncontrolled aggregation. 9-Fluorenylidene malononitrile derivatives with multiple CT interaction sites are particularly effective as preservation of a power conversion efficiency of over 90% under severe thermal stress has been accomplished. The generality of this novel strategy has been affirmed with several common donor polymers, manifesting it to be hitherto the most efficient approach to stabilized fullerene-based BHJ-OSCs.

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