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2-Methyl-4-(trifluoromethoxy)phenol is a chemical compound characterized by the molecular formula C9H9F3O2. It is a white powder with a melting point of 43-46°C and a boiling point of 108-112°C. This versatile compound is known for its applications in various industries due to its unique properties.

129676-67-1

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129676-67-1 Usage

Uses

Used in Pharmaceutical Industry:
2-Methyl-4-(trifluoromethoxy)phenol is used as a raw material for the production of pharmaceuticals. Its chemical structure allows it to be a key component in the synthesis of various medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Methyl-4-(trifluoromethoxy)phenol serves as a crucial raw material in the formulation of pesticides and other agricultural chemicals. Its presence in these products helps to enhance their effectiveness in protecting crops and controlling pests.
Used in Organic Compounds Synthesis:
2-Methyl-4-(trifluoromethoxy)phenol is utilized as an intermediate in the synthesis of various organic compounds. Its unique structure makes it a valuable building block for creating a wide range of chemical products.
Used in Dyes and Pigments Industry:
2-Methyl-4-(trifluoromethoxy)phenol is also employed in the synthesis of dyes and pigments, where it contributes to the development of vibrant colors and hues for various applications, including textiles, plastics, and inks.
Used in Personal Care Products:
Due to its antimicrobial properties, 2-Methyl-4-(trifluoromethoxy)phenol is used in personal care products to provide preservative and antimicrobial benefits, ensuring the safety and efficacy of these products.
Used in Household Disinfectants:
2-Methyl-4-(trifluoromethoxy)phenol's antimicrobial properties also make it suitable for use in household disinfectants. It helps to eliminate harmful microorganisms and maintain a clean and hygienic environment in homes.
However, it is essential to handle 2-Methyl-4-(trifluoromethoxy)phenol with care, as it can cause skin and eye irritation upon contact. Proper safety measures should be taken during its use to minimize potential risks.

Check Digit Verification of cas no

The CAS Registry Mumber 129676-67-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,6,7 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129676-67:
(8*1)+(7*2)+(6*9)+(5*6)+(4*7)+(3*6)+(2*6)+(1*7)=171
171 % 10 = 1
So 129676-67-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H7F3O2/c1-5-4-6(2-3-7(5)12)13-8(9,10)11/h2-4,12H,1H3

129676-67-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-4-(trifluoromethoxy)phenol

1.2 Other means of identification

Product number -
Other names PC8770

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:129676-67-1 SDS

129676-67-1Relevant academic research and scientific papers

Antimycotically active substituted 2-aminothiazoles

-

, (2008/06/13)

A 2-aminothiazole of the formula STR1 in which R1 represents hydrogen or alkyl and R2 represents a radical of the formula STR2 where R3, R4, R5 and R6 independently of one another in each case represent hydrogen, halogen, nitro, alkyl, alkoxy, alkoxycarbonyl, dialkylamino, alkylthio, alkylsulphinyl, alkylsulphonyl, halogenoalkyl, halogenoalkoxy, halogenoalkylthio, halogenoalkylsulphinyl or halogenoalkylsulphonyl, X represents oxygen, sulphur, sulphinyl or sulphonyl and Ar represents an unsubstituted aryl or a substituted aryl radical, and their physiologically tolerable acid addition salts.

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