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1-(2-Methoxy-5-trifluoromethylphenyl)ethanone is an organic compound with the molecular formula C10H9F3O2. It is a derivative of ethanone, featuring a methoxy group and a trifluoromethyl group attached to a phenyl ring. 1-(2-Methoxy-5-trifluoromethylphenyl)ethanone is known for its unique chemical properties and potential applications in various fields.

503464-99-1

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503464-99-1 Usage

Uses

1. Used in Pharmaceutical Industry:
1-(2-Methoxy-5-trifluoromethylphenyl)ethanone is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
2. Used in Synthesis and Evaluation of Disubstituted N1and N3-Imidazolidin-2-ones:
1-(2-Methoxy-5-trifluoromethylphenyl)ethanone is used as a key component in the synthesis and evaluation of disubstituted N1and N3-Imidazolidin-2-ones. These compounds have been identified as potential immunosuppressive agents, which can be beneficial in the treatment of autoimmune diseases and organ transplantation.
3. Used in Chemical Research:
Due to its unique structure and properties, 1-(2-Methoxy-5-trifluoromethylphenyl)ethanone is also used in chemical research for studying various reaction mechanisms and exploring new synthetic pathways. This can lead to the discovery of novel compounds with potential applications in different industries.
4. Used in Material Science:
1-(2-Methoxy-5-trifluoromethylphenyl)ethanone may also find applications in material science, where its unique properties can be utilized in the development of new materials with specific characteristics, such as improved stability, reactivity, or selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 503464-99-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,4,6 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 503464-99:
(8*5)+(7*0)+(6*3)+(5*4)+(4*6)+(3*4)+(2*9)+(1*9)=141
141 % 10 = 1
So 503464-99-1 is a valid CAS Registry Number.

503464-99-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H32652)  2'-Methoxy-5'-(trifluoromethyl)acetophenone, 97%   

  • 503464-99-1

  • 1g

  • 975.0CNY

  • Detail
  • Alfa Aesar

  • (H32652)  2'-Methoxy-5'-(trifluoromethyl)acetophenone, 97%   

  • 503464-99-1

  • 5g

  • 4918.0CNY

  • Detail

503464-99-1SDS

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 1-[2-methoxy-5-(trifluoromethyl)phenyl]ethanone

1.2 Other means of identification

Product number -
Other names 2′-Methoxy-5′-(trifluoromethyl)acetophenone

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:503464-99-1 SDS

503464-99-1Relevant articles and documents

Substituted Pyrrolidines and Methods of Use

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Paragraph 2166, (2018/04/20)

The invention discloses compounds of Formula (I) wherein R1, R2, R2A, R3, R3A, R4, and R5 are as defined herein. The present invention relates to compounds and their use in the treatment of cystic fibrosis, methods for their production, pharmaceutical compositions comprising the same, and methods of treating cystic fibrosis by administering a compound of the invention.

Discovery of potent selective orally active benzoxazepine-based orexin-2 receptor antagonists

Fujimoto, Tatsuhiko,Kunitomo, Jun,Tomata, Yoshihide,Marui, Shogo,Nishiyama, Keiji,Nakashima, Masato,Yoshikubo, Shin-Ichi,Hirai, Keisuke,Hirozane, Mariko

, p. 6414 - 6416 (2011/11/29)

During our efforts to identify a series of potent, selective, orally active human Orexin-2 Receptor (OX2R) antagonists, we elucidated structure-activity relationship (SAR) on the 7-position of a benzoxazepine scaffold by utilizing Hammett rp and Hansch-Fu

NOVEL OXIME DERIVATIVES AND THEIR USE AS ALLOSTERIC MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS

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Page/Page column 56, (2011/05/11)

The present invention provides new oxime derivatives of the general formula (I), pharmaceutical compositions containing them and their use for the treatment and/or prophylaxis of conditions associated with altered glutamatergic signalling and/or functions

THIAZOLE COMPOUNDS AS ACTIVATORS OF SOLUBLE GUANYLATE CYCLASE

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Page/Page column 32, (2010/04/03)

Disclosed are compounds of formula (I) wherein R1 and R2 are independently selected from hydrogen, halo, C1-4alkyl, C1-4alkoxy, CF3 and OCF3; -Y- represents formula (IA) R3 represents hydrogen, fluoro, chloro or C1-4alkyl; R4a and R4b each independently represent hydrogen, C1-4alkyl, C1-4alkoxy, CF3 or halo; and R5 represents a group Z-X; wherein Z is absent or represents (CH2)2 or O; and X represents formula (IB) wherein: J and L both represent CH, or one of J and L represents CH and the other represents N; when both J and L represent CH, R6 represents hydrogen, halo, CF3, C1-4alkyl or C1-4alkoxy in a meta or ortho position relative to the R7 substituent and R7 represents hydrogen, halo, CF3, OCF3, C1-4alkyl, C1-4alkoxy, CH2OH, CN, CONR8R9 or CO2H; or when one of J or L represents N, R6 represents hydrogen or halo in a meta or ortho position relative to the R7 substituent and R7 represents hydrogen, halo, CF3, C1-4alkyl, C1-4alkoxy, CH2OH, CN, CONR8R9 or CO2H; and R8 and R9 are independently selected from hydrogen and C1-4alkyl; or salts thereof which activate soluble guanylate cyclase (sGC), pharmaceutical compositions containing them, their use in medicine, and processes for their preparation.

Process for producing 4-substituted benzopyran derivatives

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, (2008/06/13)

The present invention relates to a first process for producing a 2,2-bis(fluoromethyl)-6-(perfluoroalkyl)-2H-1-benzopyran-4-carboxylic acid. The first process includes the steps of (a) reacting a 2,2-bis(fluoromethyl)-6-(perfluoroalkyl)-2H-1-benzopyran-4-

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