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241819-52-3

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241819-52-3 Usage

Description

GAMMA-PHENYL-ALPHA-(TRIFLUOROMETHYL)is a chemical compound characterized by the presence of a phenyl group attached to the gamma carbon and a trifluoromethyl group attached to the alpha carbon. This molecule is recognized for its strong electron-withdrawing properties due to the trifluoromethyl group, and its aromatic phenyl group contributes to its stability and reactivity. These unique structural features make GAMMA-PHENYL-ALPHA-(TRIFLUOROMETHYL)a versatile and valuable building block in various fields.

Uses

Used in Pharmaceutical Industry:
GAMMA-PHENYL-ALPHA-(TRIFLUOROMETHYL)is utilized as a key building block in organic synthesis for the development of pharmaceuticals. Its unique properties allow for the creation of new chemical entities that can address various medical needs.
Used in Agrochemical Industry:
In the agrochemical sector, GAMMA-PHENYL-ALPHA-(TRIFLUOROMETHYL)serves as an essential component in the synthesis of compounds used in crop protection and pest management, contributing to the development of innovative and effective products.
Used in Materials Science:
GAMMA-PHENYL-ALPHA-(TRIFLUOROMETHYL)is employed in the field of materials science for the production of advanced materials with specific properties. Its electron-withdrawing nature and aromatic stability make it suitable for creating materials with tailored characteristics for various applications.
Used in Chemical Engineering:
In chemical engineering, GAMMA-PHENYL-ALPHA-(TRIFLUOROMETHYL)is applied in the design and development of new chemical processes and reactions. Its reactivity and stability make it a valuable tool for enhancing the efficiency and selectivity of chemical transformations.

Check Digit Verification of cas no

The CAS Registry Mumber 241819-52-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,1,8,1 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 241819-52:
(8*2)+(7*4)+(6*1)+(5*8)+(4*1)+(3*9)+(2*5)+(1*2)=133
133 % 10 = 3
So 241819-52-3 is a valid CAS Registry Number.

241819-52-3 Well-known Company Product Price

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  • Aldrich

  • (514977)  γ-Phenyl-α-(trifluoromethyl)-γ-butyrolactone,mixtureofcisandtrans  97%

  • 241819-52-3

  • 514977-1G

  • 983.97CNY

  • Detail

241819-52-3SDS

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 5-phenyl-3-(trifluoromethyl)oxolan-2-one

1.2 Other means of identification

Product number -
Other names 5-phenyl-3-(trifluoromethyl)-3,4,5-trihydrofuran-2-one

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:241819-52-3 SDS

241819-52-3Upstream product

241819-52-3Downstream Products

241819-52-3Relevant articles and documents

Fluorinated butanolides and butenolides - Part 9. Synthesis of 2-(trifluoromethyl)butan-4-olides by Wittig reaction using methyl 3,3,3-trifluoropyruvate

Palecek, Jiri,Kvicala, Jaroslav,Paleta, Oldrich

, p. 177 - 183 (2007/10/03)

2-(Trifluoromethyl)butan-4-olides 13 and 14 were prepared by a three-step synthesis starting from a Wittig reagent and methyl 3,3,3-trifluoropyruvate (1) as a building block. The Wittig reaction of (2-oxoalkyl)triphenylphosphonium bromides with pyruvate 1 gave intermediate 4-oxobutenoates 8 and 9, which were stepwise selectively reduced with zinc borohydride firstly at the double bond and subsequently at the oxo group to afford unstable 4-hydroxy-2-trifluoromethylalkanoates 11 and 12, which cyclised spontaneously to the end butenolides 13 and 14.

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