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(Z)-3-(4-NITRO-PHENYL)-3-PHENYL-ACRYLIC ACID, with the molecular formula C15H11NO4, is a yellow crystalline powder derivative of acrylic acid. It features a nitrophenyl and a phenyl group, and has a molecular weight of 265.25 g/mol. This chemical compound serves as a fundamental building block in the synthesis of a variety of organic compounds and holds potential for use in pharmaceutical and agrochemical development, as well as in materials science and organic chemistry reactions.

17683-99-7

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17683-99-7 Usage

Uses

Used in Pharmaceutical and Agrochemical Development:
(Z)-3-(4-NITRO-PHENYL)-3-PHENYL-ACRYLIC ACID is used as a key intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into various drug molecules, potentially enhancing their therapeutic properties and effectiveness.
Used in Organic Chemistry Research:
(Z)-3-(4-NITRO-PHENYL)-3-PHENYL-ACRYLIC ACID is used as a reagent in organic chemistry reactions, facilitating the creation of new chemical entities and contributing to the advancement of chemical research.
Used in Materials Science:
(Z)-3-(4-NITRO-PHENYL)-3-PHENYL-ACRYLIC ACID may be utilized in the development of novel materials, potentially offering unique properties or improvements in existing material systems due to its specific molecular structure.

Check Digit Verification of cas no

The CAS Registry Mumber 17683-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,8 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17683-99:
(7*1)+(6*7)+(5*6)+(4*8)+(3*3)+(2*9)+(1*9)=147
147 % 10 = 7
So 17683-99-7 is a valid CAS Registry Number.

17683-99-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-nitrophenyl)-3-phenylprop-2-enoic acid

1.2 Other means of identification

Product number -
Other names -

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:17683-99-7 SDS

17683-99-7Relevant academic research and scientific papers

FENDILINE DERIVATIVES AND METHODS OF USE THEREOF

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Page/Page column 90, (2014/03/25)

Disclosed herein are novel derivatives of fendiline, including compounds of the formula: wherein the variables are defined herein. Also provided are pharmaceutical compositions, kits and articles of manufacture comprising these derivative compounds. Methods and intermediates useful for making the derivatives, and methods of using the derivatives, for example, for the inhibition of K-Ras plasma membrane localization, and compositions thereof, including for the treatment of cancer, are also provided.

Synthesis of coumarins via PIDA/I2-mediated oxidative cyclization of substituted phenylacrylic acids

Li, Jinming,Chen, Huiyu,Zhang-Negrerie, Daisy,Du, Yunfei,Zhao, Kang

, p. 4311 - 4320 (2013/04/24)

A variety of functionalized coumarins were synthesized from substituted phenylacrylic acids via PIDA/I2-mediated and irradiation-promoted oxidative carbon-oxygen bond formation. Our studies show that the oxygen in the pendant carboxylic acid group cyclizes favorably to the aryl ring that is cis to it. The main advantages of this method include good functional group tolerance and the transition-metal-free characteristic. The Royal Society of Chemistry 2013.

Novel azo derivatives as prodrugs of 5-aminosalicylic acid and amino derivatives with potent platelet activating factor antagonist activity

Carceller,Salas,Merlos,Giral,Ferrando,Escamilla,Ramis,García-Rafanell,Forn

, p. 3001 - 3013 (2007/10/03)

This paper describes the synthesis of a series of azo compounds able to deliver 5-aminosalicylic acid (5-ASA) and a potent platelet activating factor (PAF) antagonist in a colon-specific manner for the purpose of treating ulcerative colitis. We found it p

Diphenylpropenamides as SRS-A antagonists

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, (2008/06/13)

Certain new diphenylpropenamides having a carboxyalkanamido or a carboxyalkenamido group on one of the phenyl rings and their use for antagonizing the spasmogenic activity of the slow-reacting substance of anaphylaxis (SRS-A) in a human subject. In particular, the compounds of the invention are useful for preventing and treating certain obstructive airways diseases, notably allergic bronchial asthma, allergic rhinitis and certain skin disorders, in human subjects.

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