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2-Fluoro-4'-amino benzophenone, also known as 4'-Amino-2-fluorobenzophenone, is a chemical compound with the molecular formula C13H10FNO. It is a benzophenone derivative characterized by a fluorine atom substitution at the 2-position and an amino group at the 4'-position. 2-FLUORO-4'-AMINO BENZOPHENONE is recognized for its unique electronic and optical properties, making it a versatile building block in various chemical and pharmaceutical applications.

10055-39-7

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10055-39-7 Usage

Uses

Used in Pharmaceutical Industry:
2-Fluoro-4'-amino benzophenone is used as a key building block in the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Coatings, Adhesives, and Inks Industry:
In the manufacturing of UV-curable coatings, adhesives, and inks, 2-Fluoro-4'-amino benzophenone serves as an essential component. Its photoreactive properties enable the formulation of high-performance materials that cure rapidly under UV light, offering advantages in terms of durability and application efficiency.
Used in Organic Electronics and Materials Science:
2-Fluoro-4'-amino benzophenone has potential applications in the field of organic electronics and materials science due to its distinct electronic and optical characteristics. It can be utilized in the development of advanced materials for use in electronic devices, such as organic light-emitting diodes (OLEDs) and photovoltaic cells.
It is crucial to handle 2-Fluoro-4'-amino benzophenone with care, as it may present certain hazards associated with its use. Proper safety measures should be implemented during its production, storage, and application to mitigate any potential risks.

Check Digit Verification of cas no

The CAS Registry Mumber 10055-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,5 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10055-39:
(7*1)+(6*0)+(5*0)+(4*5)+(3*5)+(2*3)+(1*9)=57
57 % 10 = 7
So 10055-39-7 is a valid CAS Registry Number.

10055-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-aminophenyl)-(2-fluorophenyl)methanone

1.2 Other means of identification

Product number -
Other names 4-amino-2'-fluoro benzophenone

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:10055-39-7 SDS

10055-39-7Relevant academic research and scientific papers

Coumarin-surfactant modified polyoxometalate catalyzed cross dehydrogenative coupling of benzyl alcohol with the: Para -C-H of unprotected aniline

Xu, Qian,Yu, Gang,Liu, Min,Peng, Chang,Banks, M. Katherine,Xu, Weijian,Wu, Ruoxi,Lu, Yanbing

, p. 5133 - 5136 (2018/10/24)

This paper presents a novel method for synthesizing para-aminobenzophenone and its derivatives (p-ABPs) using a coumarin-surfactant modified polyoxometalate as the catalyst. Preliminary mechanistic studies indicate that the reaction has undergone an oxidative cross dehydrogenative coupling process. This method has the advantages of an easy process, a convenient raw material source, safe and green oxidants, and tolerances of several functional groups.

Therapeutic amides

-

, (2008/06/13)

Amides having formula I: STR1 wherein E, X, R2 and R3 have the meanings given in the specification, and pharmaceutically acceptable salts and pharmaceutically acceptable in vivo hydrolysable esters thereof, which are useful in the treatment of urinary incontinence. Further provided are processes for preparing the amides and pharmaceutical compositions containing them.

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