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228575-98-2

Acetamide, N-[2-[(2-aminophenyl)ethynyl]phenyl]-2,2,2-trifluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 228575-98-2 Structure

  • Basic information

    1. Product Name: Acetamide, N-[2-[(2-aminophenyl)ethynyl]phenyl]-2,2,2-trifluoro-
    2. Synonyms:
    3. CAS NO:228575-98-2
    4. Molecular Formula: C16H11F3N2O
    5. Molecular Weight: 304.271
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 228575-98-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Acetamide, N-[2-[(2-aminophenyl)ethynyl]phenyl]-2,2,2-trifluoro-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetamide, N-[2-[(2-aminophenyl)ethynyl]phenyl]-2,2,2-trifluoro-(228575-98-2)
    11. EPA Substance Registry System: Acetamide, N-[2-[(2-aminophenyl)ethynyl]phenyl]-2,2,2-trifluoro-(228575-98-2)

  • 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: 228575-98-2(Hazardous Substances Data)

228575-98-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 228575-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,8,5,7 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 228575-98:
(8*2)+(7*2)+(6*8)+(5*5)+(4*7)+(3*5)+(2*9)+(1*8)=172
172 % 10 = 2
So 228575-98-2 is a valid CAS Registry Number.

228575-98-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-[2-(2-aminophenyl)ethynyl]phenyl]-2,2,2-trifluoroacetamide

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:228575-98-2 SDS

228575-98-2Relevant articles and documents

Synthesis of indolo[1,2-c]quinazolines from 2-alkynylaniline derivatives through Pd-catalyzed indole formation/cyclization with N,N-dimethylformamide dimethyl acetal

Arcadi, Antonio,Cacchi, Sandro,Fabrizi, Giancarlo,Ghirga, Francesca,Goggiamani, Antonella,Iazzetti, Antonia,Marinelli, Fabio

supporting information, p. 2411 - 2417 (2018/10/04)

An efficient strategy for the synthesis of 6-unsubstituted indolo[1,2-c]quinazolines is described. The Pd-catalyzed reaction of o-(oaminophenylethynyl) trifluoroacetanilides with Ar-B(OH)2 afforded 2-(o-aminophenyl)-3-arylindoles, that were converted to 1

Assembly of indolo[1,2-c]quinazolines using ZnBr2-promoted domino hydroamination-cyclization

Xu, Min,Xu, Ke,Wang, Shaozhong,Yao, Zhu-Jun

supporting information, p. 4675 - 4678 (2013/08/23)

An efficient protocol to generate indolo[1,2-c]quinazolines from acyclic alkyne substrates by ZnBr2-promoted domino hydroamination-cyclization has been established. The dichotomous properties of zinc salts involving alkynophilicity and oxophili

2-(o-aminoaryl)indole derivatives via the coupling-cyclization of o-alkynylanilines with o-halotrifluoroacetanilides in the presence of a palladium catalyst

Arcadi, Antonio,Cacchi, Sandro,Fabrizi, Giancarlo,Marinelli, Fabio,Parisi, Luca M.

, p. 475 - 482 (2007/10/03)

The reaction of o-ethynylanilines with o-halotrifluoroacetanilides in the presence of PdCl2(PPh3)2 and Et3N in DMF at 90 °C affords 2-(o-trifluoroacetamidoaryl)indoles. The presence of the free amino group was found to play a crucial role in favoring the cyclization step.

6-Aryl-11H-indolo[3,2-c]quinolines through the palladium-catalyzed carbonylative cyclization of o-(o-aminophenyl)trifluoroacetanilide with aryl iodides

Cacchi, Sandro,Fabrizi, Giancarlo,Pace, Paola,Marinelli, Fabio

, p. 620 - 622 (2007/10/03)

6-Aryl-11H-indolo[3,2-c]quinolines are prepared through a straightforward palladium-catalyzed carbonylative cyclization of o-(o'- aminophenylethynyl)trifluoroacetanilide with aryl iodides followed by the cyclization of the resultant 3-acylindole derivativ

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