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Methyl 2-(3-fluoro-4-Methylphenyl)acetate is a chemical compound with the molecular formula C11H13FO2. It is an ester formed by the condensation of 2-(3-fluoro-4-methylphenyl)acetic acid and methanol. Methyl 2-(3-fluoro-4-Methylphenyl)acetate is characterized by its fruity, floral, and sweet aroma, which makes it a versatile ingredient in various industries.

787585-29-9

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787585-29-9 Usage

Uses

Used in Flavor and Fragrance Industry:
Methyl 2-(3-fluoro-4-Methylphenyl)acetate is used as a flavor or fragrance ingredient for its distinctive fruity, floral, and sweet aroma. It is incorporated into the production of perfumes, soaps, and other personal care products to enhance their scent profiles.
Used in Food Industry:
In the food industry, Methyl 2-(3-fluoro-4-Methylphenyl)acetate is used as a flavoring agent to add a unique taste and aroma to a variety of products such as beverages, candies, and baked goods, enhancing their overall sensory appeal.
Used in Pharmaceutical Industry:
Methyl 2-(3-fluoro-4-Methylphenyl)acetate also has potential applications in the pharmaceutical industry, where it serves as an intermediate in the synthesis of various drugs. Its chemical properties make it a valuable component in the development of new medicinal compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 787585-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,7,5,8 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 787585-29:
(8*7)+(7*8)+(6*7)+(5*5)+(4*8)+(3*5)+(2*2)+(1*9)=239
239 % 10 = 9
So 787585-29-9 is a valid CAS Registry Number.

787585-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 2-(3-fluoro-4-methylphenyl)acetate

1.2 Other means of identification

Product number -
Other names methyl 2-(3-fluoro-4-methylphenyl)acetate

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:787585-29-9 SDS

787585-29-9Relevant academic research and scientific papers

Enantioselective Construction of Quaternary All-Carbon Centers via Copper-Catalyzed Arylation of Tertiary Carbon-Centered Radicals

Wu, Lianqian,Wang, Fei,Chen, Pinhong,Liu, Guosheng

supporting information, p. 1887 - 1892 (2019/02/05)

An enantioselective copper-catalyzed arylation of tertiary carbon-centered radicals, leading to quaternary all-carbon stereocenters, has been developed herein. The tertiary carbon-centered radicals, including both benzylic and nonbenzylic radicals, were produced by the addition of trifluoromethyl radical to α-substituted acrylamides, and subsequently captured by chiral aryl copper(II) species to give C-Ar bonds with excellent enantioselectivity. Importantly, an acylamidyl (CONHAr) group adjacent to the tertiary carbon radical is essential for the asymmetric radical coupling. The reaction itself features broad substrate scope, excellent functional group compatibility and mild conditions.

CaSR antagonist

-

Page/Page column 40; 71, (2010/02/10)

A compound represented by the following formula (1), a pharmaceutically acceptable salt thereof or an optically active form thereof: wherein each symbol is as defined in the specification. A compound having a calcium-sensing receptor antagonistic action, a pharmaceutical composition comprising the compound, particularly a calcium receptor antagonist and a therapeutic drug for osteoporosis are provided.

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