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Methyl 3-(4-methylphenoxy)propanoate is an organic compound with the chemical formula C12H16O3. It is a colorless to pale yellow liquid with a fruity, floral, and green odor. This ester is formed by the reaction of 4-methylphenol and propionic acid, and it is widely used in the fragrance industry as a fixative and scent enhancer. It can be found in various personal care products, such as perfumes, soaps, and lotions, as well as in food flavorings. The compound is known for its ability to provide a pleasant aroma and improve the overall scent profile of the products it is used in.

7497-92-9

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7497-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7497-92-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7497-92:
(6*7)+(5*4)+(4*9)+(3*7)+(2*9)+(1*2)=139
139 % 10 = 9
So 7497-92-9 is a valid CAS Registry Number.

7497-92-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-(4-methylphenoxy)propanoate

1.2 Other means of identification

Product number -
Other names 3-p-tolyloxy-propionic acid methyl ester

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:7497-92-9 SDS

7497-92-9Relevant academic research and scientific papers

Novel compounds

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, (2008/06/13)

A compound of formula (I): STR1 or a salt, ester or amide thereof, in which Y is a group --O(CH2)m --, --(CH2)m -- or --CH=CH-- where m is an integer of from 1 to 5 n is an integer of from 4 to 14 X represents a double or triple bond, and each of A and B represents hydrogen when X is a double bond, or both A and B are absent when X is a triple bond, is useful in the treatment of allergic diseases.

Synthesis of Aryloxy Analogues of Arachidonic Acid via Wittig and Palladium Catalysed Cross-coupling Reactions

Buckle, Derek R.,Fenwick, Ashley E.,Outred, D. James,Rockell, Caroline J. M.

, p. 3144 - 3177 (2007/10/02)

The synthesis of o- and p-phenoxy analogues of arachidonic acid is described.In particular, the Wittig olefination reaction of hydroxy and alkyloxy benzaldehydes has been investigated and the products shown to be highly dependent on the solvent used.E/Z isomer control was difficult to achieve in most cases, although there was a tendency towards Z-isomer formation in dimethyl sulphoxide compared to tetrahydrofuran, particularly for the phenolic compounds.Specific Z-isomer formation was achieved by the partial reduction of alkynes derived from appropriately protected bromophenols via Heck or palladium catalysed cross-coupling reactions.

Synthesis of Peptide Alkaloids. 5. New Method for Synthesis of Ansa Peptides. Amino Acids and Peptides. 34

Schmidt, Ulrich,Lieberknecht, Albrecht,Griesser, Helmut,Talbiersky, Jorg

, p. 3261 - 3264 (2007/10/02)

Fourteen-membered para-ansa compounds and 13-membered meta-ansa compounds have been synthesized by catalytic hydrogenation of the pentafluorophenyl esters of ω-(Z)-amino carboxylic acids in 50percent and 80percent yields, respectively.

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