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35504-85-9

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35504-85-9 Usage

Description

(E)-3-(4-Fluorobenzoyl)acrylic acid, also known as 4-Fluorocinnamic acid, is an organic compound with the molecular formula C10H7FO2. It is a derivative of cinnamic acid with a fluorine substituent on the benzene ring. This chemical is commonly used in organic synthesis and pharmaceutical research as an intermediate for the production of various pharmaceuticals and agrochemicals. It possesses potential biological and pharmacological activities, making it a valuable compound in medicinal chemistry. Additionally, (E)-3-(4-Fluorobenzoyl)acrylic acid has the potential to be used in the development of new drug formulations and therapies due to its unique chemical structure and properties.

Uses

Used in Pharmaceutical Research:
(E)-3-(4-Fluorobenzoyl)acrylic acid is used as an intermediate in the synthesis of various pharmaceuticals for its potential biological and pharmacological activities.
Used in Agrochemical Production:
(E)-3-(4-Fluorobenzoyl)acrylic acid is used as an intermediate in the production of agrochemicals, contributing to the development of new compounds for agricultural applications.
Used in Medicinal Chemistry:
(E)-3-(4-Fluorobenzoyl)acrylic acid is used as a valuable compound in medicinal chemistry for its potential to be utilized in the development of new drug formulations and therapies.
Used in Organic Synthesis:
(E)-3-(4-Fluorobenzoyl)acrylic acid is used as a key component in organic synthesis, allowing for the creation of a variety of chemical compounds with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 35504-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,0 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 35504-85:
(7*3)+(6*5)+(5*5)+(4*0)+(3*4)+(2*8)+(1*5)=109
109 % 10 = 9
So 35504-85-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H7FO3/c11-8-3-1-7(2-4-8)9(12)5-6-10(13)14/h1-6H,(H,13,14)/b6-5+

35504-85-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (E) 4-(4-fluorophenyl)-4-oxo-2-butenoic acid

1.2 Other means of identification

Product number -
Other names β-(p-fluorobenzoyl)acrylic 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:35504-85-9 SDS

35504-85-9Relevant articles and documents

ENHANCER OF FERTILIZATION FUNCTION OF SPERM

-

, (2022/04/09)

An object of the present invention is to provide an agent for enhancing fertilization function of a mammal sperm, which comprises a low molecular compound which can be produced relatively easily and inexpensively as an active ingredient, and a method for enhancing fertilization function of a mammal sperm and a method for preparing a mammal fertilized egg, which use a low molecular compound which can be produced relatively easily and inexpensively. An agent comprising one or more compounds selected from the group consisting of compounds of the following formula (I0), formula (II), and formula (III), and physiologically acceptable salts thereof when R3 is OH is used as an agent for enhancing fertilization function of a mammal sperm.

Microwave-assisted synthesis of 4-oxo-2-butenoic acids by aldol-condensation of glyoxylic acid

Gai, Conghao,Leach, Andrew G.,Liu, Hang,Sprenger, Lukas J.,Uguen, Mélanie,Waring, Michael J.

, p. 30229 - 30236 (2021/10/20)

4-Oxobutenoic acids are useful as biologically active species and as versatile intermediates for further derivatisation. Currently, routes to their synthesis can be problematic and lack generality. Reaction conditions for the synthesis of 4-oxo-2-butenoic

Design, synthesis, and bioevaluation of a novel class of (E)-4-oxo-crotonamide derivatives as potent antituberculosis agents

Ren, Jinfeng,Xu, Jian,Zhang, Guoning,Xu, Changliang,Zhao, LiLi,You, XueFu,Wang, Yucheng,Lu, Yu,Yu, Liyan,Wang, Juxian

supporting information, p. 539 - 543 (2019/01/09)

A series of novel (E)-4-oxo-2-crotonamide derivatives were designed and synthesized to find potent antituberculosis agents. All the target compounds were evaluated for their in vitro activity against Mycobacterium tuberculosis H37Rv(MTB). Results reveal that 4-phenyl moiety at part A and short methyl group at part C were found to be favorable. Most of the derivatives displayed promising activity against MTB with MIC ranging from 0.125 to 4 μg/mL. Especially, compound IIIa16 was found to have the best activity with MIC of 0.125 μg/mL against MTB and with MIC in the range of 0.05–0.48 μg/mL against drug-resistant clinical MTB isolates.

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