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2-methyl-4-(trifluoromethyl)phenol, also known as trifluorosaligenin, is a chemical compound characterized by the molecular formula C8H7F3O. It presents as a white crystalline solid with a melting point of 43-44°C and exhibits insolubility in water. 2-methyl-4-(trifluoromethyl)phenol is recognized for its versatile applications across different industries, primarily due to its bactericidal and fungicidal properties.

77227-90-8

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77227-90-8 Usage

Uses

Used in Industrial and Agricultural Applications:
2-methyl-4-(trifluoromethyl)phenol is utilized as a bacteriostat and fungicide, serving to inhibit the growth of bacteria and fungi in various settings. Its effectiveness in controlling microbial growth makes it a valuable asset in preserving the quality and safety of products in these industries.
Used in Pharmaceutical Production:
As an intermediate in the synthesis of pharmaceuticals, 2-methyl-4-(trifluoromethyl)phenol plays a crucial role in the development of new drugs. Its chemical properties allow it to be a building block for creating a range of medicinal compounds, contributing to advancements in healthcare.
Used in Organic Compound Synthesis:
2-methyl-4-(trifluoromethyl)phenol is also employed as an intermediate in the production of other organic compounds, highlighting its importance in the realm of organic chemistry and the creation of novel materials and substances with potential applications in various fields.
Used in Environmental Research:
2-methyl-4-(trifluoromethyl)phenol has been identified as a potential environmental contaminant, prompting research into its impact on human health and the environment. This role is significant for understanding and mitigating the effects of chemical contaminants in ecosystems and on public health.

Check Digit Verification of cas no

The CAS Registry Mumber 77227-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,2 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77227-90:
(7*7)+(6*7)+(5*2)+(4*2)+(3*7)+(2*9)+(1*0)=148
148 % 10 = 8
So 77227-90-8 is a valid CAS Registry Number.

77227-90-8Relevant academic research and scientific papers

MODULATORS OF MAS-RELATED G-PROTEIN RECEPTOR X4 AND RELATED PRODUCTS AND METHODS

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Page/Page column 110; 120, (2020/10/18)

Methods are provided for modulating MRGPR X4 generally, or for treating a MRGPR X4 dependent condition more specifically, by contacting the MRGPR X4 or administering to a subject in need thereof, respectively, an effective amount of a compound having the structure of Formula (I): (I) or a pharmaceutically acceptable isomer, racemate, hydrate, solvate, isotope, or salt thereof, wherein n, x, A, Q1, Q2, Z, R, R1, R2, R3, R4 and R5 are as defined herein. Pharmaceutical compositions containing such compounds, as well as to compounds themselves, are also provided.

UBIQUITIN-SPECIFIC-PROCESSING PROTEASE 7 (USP7) MODULATORS AND USES THEREOF

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Paragraph 0672, (2019/05/24)

Disclosed herein, inter alia, compounds and methods of use thereof for the modulation of USP7 activity.

ANTICANCER COMPOUNDS

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Paragraph 0178, (2018/05/03)

The invention provides compounds having the general formula I: and salts thereof, wherein the variables RA, RB, RC, L1, L2, L3, A, B, C, X, Y, Z, E, m, n, and p have the meaning as describe

N-(1-Benzyl-3,5-dimethyl?1H?pyrazol-4-yl)benzamides: Antiproliferative activity and effects on mTORC1 and autophagy

Ai, Teng,Willett, Rose,Williams, Jessica,Ding, Rui,Wilson, Daniel J.,Xie, Jiashu,Kim, Do-Hyung,Puertollano, Rosa,Chen, Liqiang

supporting information, p. 90 - 95 (2017/12/13)

Guided by antiproliferative activity in MIA PaCa-2 cells, we have performed preliminary structure?activity relationship studies on N-(1-benzyl-3,5-dimethyl-1H-pyrazol-4-yl)benzamides. Two selected compounds showed submicromolar antiproliferative activity

Syntheses and bioactivity of o- or p-trifluoromethylphenyl phosphates

Zhou, Xinming,He, Yantao,Wang, Miao,Ding, Yixiang

experimental part, p. 651 - 659 (2009/11/30)

o- and p-Trifluoromethylphenyl phosphates designed as mechanism-based phosphotyrosine phosphatase inactivators have been prepared. Some of them show herbicidal activities.

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