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(E)-3-[3-(trifluoromethyl)phenyl]acrylonitrile, also known as 2-(3-trifluoromethylphenyl)-acrylonitrile, is a chemical compound characterized by its molecular formula C10H6F3N. It is a highly reactive and toxic liquid with a strong and distinct odor. (E)-3-[3-(trifluoromethyl)phenyl]acrylonitrile is recognized for its versatile applications in the synthesis of various organic compounds, making it a valuable asset in chemical research laboratories. However, due to its toxic and irritant properties, it requires careful handling and should only be used in well-ventilated areas with proper safety equipment.

58177-64-3

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58177-64-3 Usage

Uses

Used in Polymer Production:
(E)-3-[3-(trifluoromethyl)phenyl]acrylonitrile is used as a monomer in the polymer industry for the production of polymers with specific properties. Its unique structure contributes to the development of polymers with enhanced characteristics, such as improved strength, durability, and chemical resistance.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, (E)-3-[3-(trifluoromethyl)phenyl]acrylonitrile serves as a key intermediate in the synthesis of various drugs. Its reactive nature allows for the creation of new pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemicals:
(E)-3-[3-(trifluoromethyl)phenyl]acrylonitrile is also utilized in the agrochemical industry for the development of new pesticides and other agricultural chemicals. Its incorporation into these products can lead to improved effectiveness and targeted action against pests and diseases.
Used in Chemical Research:
As a highly reactive compound, (E)-3-[3-(trifluoromethyl)phenyl]acrylonitrile is commonly used in chemical research laboratories for the synthesis of various organic compounds. Its unique properties make it an essential tool for researchers in the development of new chemical entities and the exploration of novel reaction pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 58177-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,7 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58177-64:
(7*5)+(6*8)+(5*1)+(4*7)+(3*7)+(2*6)+(1*4)=153
153 % 10 = 3
So 58177-64-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H6F3N/c11-10(12,13)9-5-1-3-8(7-9)4-2-6-14/h1-5,7H/b4-2+

58177-64-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name E-3-(3-(trifluoromethyl)phenyl)acrylonitrile

1.2 Other means of identification

Product number -
Other names (E)-3-(3-Trifluoromethyl-phenyl)-acrylonitrile

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:58177-64-3 SDS

58177-64-3Downstream Products

58177-64-3Relevant academic research and scientific papers

Development and Utilization of a Palladium-Catalyzed Dehydration of Primary Amides to Form Nitriles

Al-Huniti, Mohammed H.,Rivera-Chávez, José,Colón, Katsuya L.,Stanley, Jarrod L.,Burdette, Joanna E.,Pearce, Cedric J.,Oberlies, Nicholas H.,Croatt, Mitchell P.

supporting information, p. 6046 - 6050 (2018/09/27)

A palladium(II) catalyst, in the presence of Selectfluor, enables the efficient and chemoselective transformation of primary amides into nitriles. The amides can be attached to aromatic rings, heteroaromatic rings, or aliphatic side chains, and the reactions tolerate steric bulk and electronic modification. Dehydration of a peptaibol containing three glutamine groups afforded structure-activity relationships for each glutamine residue. Thus, this dehydration can act similarly to an alanine scan for glutamines via synthetic mutation.

5, 7-SUBSTITUTED-IMIDAZO [1, 2-C] PYRIMIDINES AS INHIBITORS OF JAK KINASES

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Page/Page column 80, (2011/11/01)

Compounds of Formula I: (Formula should be inserted here) and stereoisomers and pharmaceutically acceptable salts and solvates thereof in which R1, R2, R3, R4, R5, R6, R7, X1 and X2 have the meanings given in the specification, are inhibitors of one or more JAK kinases and are useful in the treatment of autoimmune diseases, inflammatory diseases, rejection of transplanted organs, tissues and cells, as well as hematologic disorders and malignancies and their co-morbidities.

DATA PROCESSING DEVICE, PARTICULARLY A SET-TOP BOX FOR CONNECTION TO A RECEIVER, INPUT DEVICE FOR THE CONTROL OF A DATA PROCESSING DEVICE, AND METHOD FOR OPERATING A DATA PROCESSING DEVICE

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Page/Page column 26, (2008/06/13)

The invention relates to a data processing device, particularly a set-top box, and a method for operating the data processing device (16). The data processing device (16) is provided for the connection to a receiver (15) and a communication network. The data processing device (16) is configured to receive and process data sent from the communication network, comprising content data (2) and at least one identification date (3), and to transmit the processed data to the receiver (15) for the output thereof. The data processing device (16) is further configured to receive and process a code sent by an input device of the data processing device and/or of the receiver (15), the code being associated with a certain identification date (3) of the identification data. In response to the receipt of the code, a communication connection is established between the data processing device (16), or a communication terminal (19), and a unit of the communication network, which is associated with the certain identification date (3).

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