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14618-49-6

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14618-49-6 Usage

Description

N,N-Diallyl-2,2,2-Trifluoroacetamide (DAF) is an organic building block utilized in chemical synthesis, characterized by its density and refractive index at 25°C, which are 1.1300g/cm3 and 1.4130, respectively. It is known for its potential use in various chemical reactions, particularly the ring-closing metathesis (RCM) reaction.

Uses

Used in Chemical Synthesis:
N,N-Diallyl-2,2,2-Trifluoroacetamide is used as a substrate for the ring-closing metathesis (RCM) reaction, a key process in the synthesis of various complex organic compounds. Its role in this reaction is crucial for the formation of cyclic structures, which are essential in the development of pharmaceuticals, agrochemicals, and advanced materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N,N-Diallyl-2,2,2-Trifluoroacetamide is used as a building block for the synthesis of novel drug candidates. Its unique structure allows for the creation of molecules with specific biological activities, potentially leading to the development of new treatments for various diseases.
Used in Material Science:
N,N-Diallyl-2,2,2-Trifluoroacetamide is also used in the field of material science, where it contributes to the development of advanced materials with tailored properties. Its involvement in the synthesis of complex organic compounds can lead to the creation of materials with improved mechanical, electrical, or optical characteristics, depending on the specific application.
Used in Agrochemical Industry:
In the agrochemical industry, N,N-Diallyl-2,2,2-Trifluoroacetamide is used as a starting material for the synthesis of new pesticides or other agrochemical products. Its role in the RCM reaction allows for the creation of cyclic structures that can exhibit specific biological activities, potentially leading to more effective and targeted pest control solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 14618-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,1 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14618-49:
(7*1)+(6*4)+(5*6)+(4*1)+(3*8)+(2*4)+(1*9)=106
106 % 10 = 6
So 14618-49-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H10F3NO/c1-3-5-12(6-4-2)7(13)8(9,10)11/h3-4H,1-2,5-6H2

14618-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trifluoro-N,N-bis(prop-2-enyl)acetamide

1.2 Other means of identification

Product number -
Other names N-trifluoroacetyl diallylamine

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:14618-49-6 SDS

14618-49-6Relevant articles and documents

Electrochemical approach to trifluoroacetamide synthesis from 1,1,1-trichloro-2,2,2-trifluoroethane (CFC-113a) catalyzed by B12complex

Moniruzzaman, Mohammad,Yano, Yoshio,Ono, Toshikazu,Hisaeda, Yoshio,Shimakoshi, Hisashi

, (2021/03/09)

One-pot synthetic approach to produce trifluoroacetamide has been developed using an electrochemical method with the B12 complex as a catalyst under mild conditions, in open air at room temperature. Thirty examples of trifluoroacetamide were synthesized from 1,1,1-trichloro-2,2,2-trifluoroethane (CFC-113a) in moderate to good yields. This user-friendly strategy is compatible with a broad range of trifluoroacetamide syntheses.

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