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75706-11-5

2-ACETYL-3-ETHOXY-N-(4-TRIFLUOROMETHYLPHENYL)ACRYLAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 75706-11-5 Structure

  • Basic information

    1. Product Name: 2-ACETYL-3-ETHOXY-N-(4-TRIFLUOROMETHYLPHENYL)ACRYLAMIDE
    2. Synonyms: 2-ACETYL-3-ETHOXY-N-(4-TRIFLUOROMETHYLPHENYL)ACRYLAMIDE
    3. CAS NO:75706-11-5
    4. Molecular Formula: C14H14F3NO3
    5. Molecular Weight: 301.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 75706-11-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 449.2°C at 760 mmHg
    3. Flash Point: 225.5°C
    4. Appearance: /
    5. Density: 1.279g/cm3
    6. Vapor Pressure: 2.92E-08mmHg at 25°C
    7. Refractive Index: 1.509
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-ACETYL-3-ETHOXY-N-(4-TRIFLUOROMETHYLPHENYL)ACRYLAMIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-ACETYL-3-ETHOXY-N-(4-TRIFLUOROMETHYLPHENYL)ACRYLAMIDE(75706-11-5)
    12. EPA Substance Registry System: 2-ACETYL-3-ETHOXY-N-(4-TRIFLUOROMETHYLPHENYL)ACRYLAMIDE(75706-11-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 75706-11-5(Hazardous Substances Data)

75706-11-5 Usage

Chemical compound

2-ACETYL-3-ETHOXY-N-(4-TRIFLUOROMETHYLPHENYL)ACRYLAMIDE

Molecular structure

Complex

Composition

Acetyl, ethoxy, acrylamide groups, trifluoromethylphenyl substituent
Derivative of acrylamide

Uses

Production of polymers, laboratory reagent

Potential applications

Pharmaceuticals, agrochemicals

Trifluoromethylphenyl group

Enhances biological activity

Acetyl and ethoxy groups

Related to solubility and reactivity
Further research and testing needed to understand uses and effects

Check Digit Verification of cas no

The CAS Registry Mumber 75706-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,0 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75706-11:
(7*7)+(6*5)+(5*7)+(4*0)+(3*6)+(2*1)+(1*1)=135
135 % 10 = 5
So 75706-11-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H14F3NO3/c1-3-21-8-12(9(2)19)13(20)18-11-6-4-10(5-7-11)14(15,16)17/h4-8H,3H2,1-2H3,(H,18,20)/b12-8-

75706-11-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(ethoxymethylidene)-3-oxo-N-[4-(trifluoromethyl)phenyl]butanamide

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:75706-11-5 SDS

75706-11-5Relevant articles and documents

Exploiting intramolecular hydrogen bonding for the highly (: Z)-selective & metal free synthesis of amide substituted β-aminoenones

Subramaniam, Palaniraja,Ramasubbu, Chandrasekaran,Athiramu, Selvaraj

supporting information, p. 2541 - 2545 (2017/07/17)

Herein, we report the metal free and intramolecular hydrogen bonding (IMHB) directed (Z)-selective synthesis of amide substituted β-aminoenones. Systematically, we confirm the role of dual IMHB (CO?H-N) on the Z-direction using single-crystal X-ray analysis and 1D and 2D NMR studies. High stereoselectivity, atom efficiency, excellent yields and high purity are achieved by mere filtration. We avoid column purification and the formed by-product in the process is environmentally friendly.

Synthesis and immunosuppressant activity of pyrazole carboxamides

Wang, Alan X.,Xie, Qinghua,Lane, Ben,Mollison, Karl W.,Hsieh, Gin C.,Marsh, Kennan,Sheets, Michael P.,Luly, Jay R.,Coghlan, Michael J.

, p. 2787 - 2792 (2007/10/03)

A series of novel pyrazole carboxamides sis disclosed that demonstrate strong immunosuppressant activity in rodent and human mixed leukocyte response (MLR) assays (IC50 1 μM). The synthesis, biological activity, mode of action, and pharmacokinetic properties of this new lead series are discussed.

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