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2-Methoxy-4-(trifluoromethyl)aniline, with the molecular formula C8H8F3NO, is an aromatic amine featuring a methoxy group and a trifluoromethyl group attached to the benzene ring. 2-METHOXY-4-(TRIFLUOROMETHYL)ANILINE is recognized for its role as a versatile intermediate in the synthesis of pharmaceuticals, agrochemicals, and organic compounds, as well as a building block for dyes, pigments, and polymers. The presence of the trifluoromethyl group is known to enhance the biological activity of compounds, making 2-Methoxy-4-(trifluoromethyl)aniline a significant component in medicinal chemistry research. It also serves as a reagent in organic synthesis and a UV absorber in specific applications. However, due to its potential hazards, including skin and eye irritation and harmful effects if ingested or inhaled, careful handling is required.

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  • 158727-56-1 Structure
  • Basic information

    1. Product Name: 2-METHOXY-4-(TRIFLUOROMETHYL)ANILINE
    2. Synonyms: 2-METHOXY-4-(TRIFLUOROMETHYL)ANILINE;2-Methoxy-4-(trifluoromethyl)aniline, 2-Amino-5-(trifluoromethyl)anisole
    3. CAS NO:158727-56-1
    4. Molecular Formula: C8H8F3NO
    5. Molecular Weight: 191.1504296
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 158727-56-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C(protect from light)
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-METHOXY-4-(TRIFLUOROMETHYL)ANILINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-METHOXY-4-(TRIFLUOROMETHYL)ANILINE(158727-56-1)
    11. EPA Substance Registry System: 2-METHOXY-4-(TRIFLUOROMETHYL)ANILINE(158727-56-1)
  • 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: 158727-56-1(Hazardous Substances Data)

158727-56-1 Usage

Uses

Used in Pharmaceutical Industry:
2-Methoxy-4-(trifluoromethyl)aniline is used as an intermediate in the synthesis of various pharmaceuticals for its ability to enhance the biological activity of compounds, contributing to the development of new medications.
Used in Agrochemical Industry:
In agrochemicals, 2-Methoxy-4-(trifluoromethyl)aniline serves as an intermediate, playing a crucial role in the creation of effective crop protection agents and other agricultural products.
Used in Organic Compounds Synthesis:
2-Methoxy-4-(trifluoromethyl)aniline is used as a building block in the preparation of various organic compounds, leveraging its chemical properties to form a wide range of products.
Used in Dyes and Pigments Industry:
2-METHOXY-4-(TRIFLUOROMETHYL)ANILINE is utilized as a building block for the preparation of dyes and pigments, where its unique structure contributes to the color and properties of the final products.
Used in Polymers Industry:
2-Methoxy-4-(trifluoromethyl)aniline is used in the synthesis of polymers, where its structural features can influence the polymer's characteristics, such as stability and reactivity.
Used as a Reagent in Organic Synthesis:
In organic synthesis, 2-Methoxy-4-(trifluoromethyl)aniline functions as a reagent, facilitating various chemical reactions and contributing to the formation of desired products.
Used as a UV Absorber:
2-Methoxy-4-(trifluoromethyl)aniline is employed as a UV absorber in certain applications, protecting materials from the damaging effects of ultraviolet radiation.

Check Digit Verification of cas no

The CAS Registry Mumber 158727-56-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,7,2 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 158727-56:
(8*1)+(7*5)+(6*8)+(5*7)+(4*2)+(3*7)+(2*5)+(1*6)=171
171 % 10 = 1
So 158727-56-1 is a valid CAS Registry Number.

158727-56-1 Well-known Company Product Price

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  • Aldrich

  • (JWP00404)  2-Methoxy-4-trifluoromethyl-aniline  AldrichCPR

  • 158727-56-1

  • JWP00404-1G

  • 4,832.10CNY

  • Detail

158727-56-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methoxy-4-(trifluoromethyl)aniline

1.2 Other means of identification

Product number -
Other names PC4598

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:158727-56-1 SDS

158727-56-1Relevant articles and documents

Vapochromic Luminescent π-Conjugated Systems with Reversible Coordination-Number Control of Hypervalent Tin(IV)-Fused Azobenzene Complexes

Gon, Masayuki,Tanaka, Kazuo,Chujo, Yoshiki

, p. 7561 - 7571 (2021)

The dynamic and reversible changes of coordination numbers between five and six in solution and solid states, based on hypervalent tin(IV)-fused azobenzene (TAz) complexes, are reported. It was found that the TAz complexes showed deep-red emission owing t

METHODS AND COMPOUNDS FOR RESTORING MUTANT p53 FUNCTION

-

, (2021/04/02)

Mutations in oncogenes and tumor suppressors contribute to the development and progression of cancer. The present disclosure describes compounds and methods to recover wild-type function to p53 mutants. The compounds of the present invention can bind to mutant p53 and restore the ability of the p53 mutant to bind DNA and activate downstream effectors involved in tumor suppression. The disclosed compounds can be used to reduce the progression of cancers that contain a p53 mutation.

QUINOLINONE DERIVATIVES AS METHIONINE ADENOSYLTRANSFERASE 2A INHIBITORS

-

, (2021/12/31)

Disclosed herein are certain quinolinone derivatives of Formula (A) that are methionine adenosyltransferase 2A (MAT2A) inhibitors. Also disclosed are pharmaceutical compositions comprising such compounds and methods of treating diseases treatable by inhibition of MAT2A such as cancer, including cancers characterized by reduced or absence of methylthioadenosine phosphorylase (MTAP) activity.

Preparation method of trifluoromethylamine

-

Paragraph 0023-0026; 0027-0045; 0046-0056; 0076-0086, (2018/09/28)

The invention relates to a preparation method of trifluoromethylamine. The method includes the following steps that aromatic amine shown in the formula (1) and a trifluoromethyl reagent shown in the formula (2) react in a solvent under the condition that an alkali and/or nickel compound exists, and the trifluoromethylamine compound shown in the formula (3) is generated. According to the preparation method of trifluoromethylamine, aromatic amine and 1-trifluoromethyl-1,2-iodobenzoyl-3(H)-ketone serve as raw materials and react under the condition that the alkali and/or nickel compound exists through the amino positioning effect on aromatic nucleus. The synthesis steps of the method are simple, the cost of the raw materials is low, the production cost of trifluoromethylamine can be greatly reduced, and large-scale industrialized production is promoted.

Nickel-Catalyzed Direct C-H Trifluoromethylation of Free Anilines with Togni's Reagent

Gao, Xianying,Geng, Yang,Han, Shuaijun,Liang, Apeng,Li, Jingya,Zou, Dapeng,Wu, Yusheng,Wu, Yangjie

supporting information, p. 3732 - 3735 (2018/07/22)

An efficient nickel-catalyzed C-H trifluoromethylation for the synthesis of trifluoromethylated free anilines using Togni's reagent has been developed. This approach exhibits a good functional group tolerance, good regioselectivity, and chemoselectivity under mild conditions. The newly developed economical one-step method is a better alternative to synthesize trifluoromethylated free anilines.

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