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Methyl 2-methyl-3-(trifluoromethyl)benzoate is a synthetic organic compound belonging to the benzoate family, with the chemical formula C10H9F3O2. It is characterized by the presence of a trifluoromethyl group attached to a benzoate ester, which likely contributes to its unique properties. Although specific information about its physical characteristics is limited, it is expected to share common features with other benzoates, such as being slightly soluble in water and having a sweet or fruity smell. As a chemical compound, it should be handled with care and appropriate safety measures.

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  • 346603-63-2 Structure
  • Basic information

    1. Product Name: Methyl 2-Methyl-3-(trifluoroMethyl)benzoate
    2. Synonyms: Methyl 2-Methyl-3-(trifluoroMethyl)benzoate;2-Methyl-3-(trifluoromethyl)benzoic acid methyl ester
    3. CAS NO:346603-63-2
    4. Molecular Formula: C10H9F3O2
    5. Molecular Weight: 218.1724696
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 346603-63-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 220℃
    3. Flash Point: 68℃
    4. Appearance: /
    5. Density: 1.231
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: Methyl 2-Methyl-3-(trifluoroMethyl)benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 2-Methyl-3-(trifluoroMethyl)benzoate(346603-63-2)
    11. EPA Substance Registry System: Methyl 2-Methyl-3-(trifluoroMethyl)benzoate(346603-63-2)
  • 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: 346603-63-2(Hazardous Substances Data)

346603-63-2 Usage

Uses

Used in Chemical Research:
Methyl 2-methyl-3-(trifluoromethyl)benzoate is used as a research compound for its unique property of having a trifluoromethyl group attached to a benzoate ester. This characteristic makes it valuable in various chemical research applications, where its properties can be explored and utilized for the development of new compounds and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, methyl 2-methyl-3-(trifluoromethyl)benzoate can be used as an intermediate or building block in the synthesis of various pharmaceutical compounds. Its unique structure and properties may contribute to the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
Methyl 2-methyl-3-(trifluoromethyl)benzoate may also find applications in the agrochemical industry, where it can be used as a precursor or intermediate in the synthesis of various agrochemicals, such as pesticides and herbicides. Its unique properties may contribute to the development of more effective and environmentally friendly agrochemicals.
Used in Flavor and Fragrance Industry:
Due to its potential sweet or fruity smell, methyl 2-methyl-3-(trifluoromethyl)benzoate can be used as a flavoring agent or fragrance ingredient in the food and cosmetics industries. Its unique aroma profile may add a distinct character to various products, enhancing their sensory appeal.

Check Digit Verification of cas no

The CAS Registry Mumber 346603-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,6,6,0 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 346603-63:
(8*3)+(7*4)+(6*6)+(5*6)+(4*0)+(3*3)+(2*6)+(1*3)=142
142 % 10 = 2
So 346603-63-2 is a valid CAS Registry Number.

346603-63-2SDS

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 Methyl 2-methyl-3-(trifluoromethyl)benzoate

1.2 Other means of identification

Product number -
Other names Methyl 2-methyl-3-trifluoromethylbenzoate

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:346603-63-2 SDS

346603-63-2Relevant articles and documents

Pyridazone derivative and its uses

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Paragraph 0127, (2022/01/12)

The present invention belongs to the pharmaceutical field, specifically relates to a pyridazone derivative and its uses, compounds thereof and pharmaceutically acceptable salts, solvates including hydrates, polycrystallines, prodrugs, co-crystallines, tau

Isosteric analogs of lenalidomide and pomalidomide: Synthesis and biological activity

Ruchelman, Alexander L.,Man, Hon-Wah,Zhang, Weihong,Chen, Roger,Capone, Lori,Kang, Jian,Parton, Anastasia,Corral, Laura,Schafer, Peter H.,Babusis, Darius,Moghaddam, Mehran F.,Tang, Yang,Shirley, Michael A.,Muller, George W.

, p. 360 - 365 (2013/02/23)

A series of analogs of the immunomodulary drugs lenalidomide (1) and pomalidomide (2), in which the amino group is replaced with various isosteres, was prepared and assayed for immunomodulatory activity and activity against cancer cell lines. The 4-methyl and 4-chloro analogs 4 and 15, respectively, displayed potent inhibition of tumor necrosis factor-α (TNF-α) in LPS-stimulated hPBMC, potent stimulation of IL-2 in a human T cell co-stimulation assay, and anti-proliferative activity against the Namalwa lymphoma cell line. Both of these analogs displayed oral bioavailability in rat.

ISOINDOLINONE DERIVATIVES

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Page/Page column 10, (2012/11/13)

The present invention relates to compounds of the formula I, as well as pharmaceutically-acceptable salts thereof, pharmaceutical compositions containing said compounds and methods of using said compounds in the treatment or prophylaxis of diseases and disorders. The compounds and compositions disclosed herein are glucokinase activators useful for the treatment or prophylaxis of metabolic diseases and disorders, for example diabetes mellitus, including type II diabetes mellitus.

THIAZOLOPYRIMIDINONE DERIVATIVES AS PI3 KINASE INHIBITORS

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Page/Page column 101, (2010/12/18)

This invention relates to the use of thiazolopyrimidinone derivatives for the modulation, notably the inhibition of the activity or function of the phosphoinositide 3' OH kinase family (hereinafter PI3 kinases), suitably, PI3Kα, PI3Kδ, PI3Kβ, and/or PI3Kγ

Tricyclic compounds

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Page/Page column 62-63, (2010/01/31)

The present invention is to provide novel tricyclic compounds having leukotriene antagonistic action and represented by the formula: wherein R1 represents a halogen atom, etc., R2 represents a nitro group, etc., A represents a 5-membered or a 6-membered heteroaromatic ring group containing 1 to 3 hetero atoms selected from the group consisting of a nitrogen atom, an oxygen atom and a sulfur atom, etc., B represents a formula: —OCH2—, etc., X represents a sulfur atom, etc., Y represents C1-C10 alkylene group which may have a halogen atom, etc. as a substituent(s), Z represents a carboxyl group whic may be protected, etc., represents a single bond or a double bond, m is an integer of 1 to 4, n is an integer of 1 to 3, or a pharmaceutically acceptable salt thereof.

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