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Methyl 4-formyl-3-methylbenzoate is a chemical compound with the molecular formula C10H10O3. It is a white crystalline solid that is commonly used in the synthesis of various organic compounds and pharmaceuticals. Methyl 4-formyl-3-methylbenzoate is also known for its pleasant, fruity odor, making it a popular choice in the production of perfumes and flavorings. Methyl 4-formyl-3-methylbenzoate is considered to be relatively stable under normal conditions, but may react with strong oxidizing agents. Careful handling and adherence to proper safety protocols are essential when working with Methyl 4-formyl-3-methylbenzoate in a laboratory or industrial setting.

24078-24-8

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24078-24-8 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 4-formyl-3-methylbenzoate is used as an intermediate in the synthesis of various pharmaceuticals for its versatile chemical structure and reactivity, contributing to the development of new drugs and medications.
Used in Perfumery:
Methyl 4-formyl-3-methylbenzoate is used as a fragrance ingredient for its pleasant, fruity odor, enhancing the scent profiles of various perfumes and colognes.
Used in Flavor Industry:
Methyl 4-formyl-3-methylbenzoate is used as a flavoring agent to impart a fruity taste to food products, beverages, and other consumables, adding depth and complexity to their flavor profiles.
Used in Organic Synthesis:
Methyl 4-formyl-3-methylbenzoate is used as a key building block in the synthesis of a wide range of organic compounds, including specialty chemicals, dyes, and other industrial products, due to its reactive functional groups and structural properties.

Check Digit Verification of cas no

The CAS Registry Mumber 24078-24-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,7 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24078-24:
(7*2)+(6*4)+(5*0)+(4*7)+(3*8)+(2*2)+(1*4)=98
98 % 10 = 8
So 24078-24-8 is a valid CAS Registry Number.

24078-24-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-formyl-3-methylbenzoate

1.2 Other means of identification

Product number -
Other names -

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:24078-24-8 SDS

24078-24-8Relevant academic research and scientific papers

P2X3 MODULATORS

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Paragraph 00241, (2021/08/20)

Provided herein are P2X3 modulators and methods of utilizing P2X3 modulators in the treatment of diseases, disorders, or conditions. Also described herein are pharmaceutical compositions containing such compounds.

LSD1 INHIBITORS AND USES THEREOF

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Paragraph 00181, (2016/11/17)

Provided are novel compounds of Formula (I) and pharmaceutically acceptable salts thereof, which are useful for treating a variety of diseases, disorders or conditions, associated with LSDl. Also provided are pharmaceutical compositions comprising the novel compounds of Formula (I), pharmaceutically acceptable salts thereof, and methods for their use in treating one or more diseases, disorders or conditions, associated with LSDl.

Efficient three-component synthesis of diversely substituted tetrahydro-1H-cyclopenta[c]quinolines

Ni?o, Patricia,Caba, Marta,Aguilar, Nuria,Terricabras, Emma,Albericio, Fernando,Fernàndez, Joan-Carles

, p. 854 - 881 (2017/01/18)

The synthesis of highly functionalized substituted tetrahydro-1H-cyclopenta[c]quinoline (I) and its reduced derivatives hexahydro-1H-cyclopenta[c]quinolines (II) via Povarov reaction in high diastereoselectivity and high to moderate yields is described he

INHIBITORS OF HEPATITIS C VIRUS POLYMERASE

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Paragraph 560; 562, (2016/10/11)

The present invention provides, among other things, compounds represented by the general Formula I: (I) and pharmaceutically acceptable salts thereof, wherein L and A (and further substituents) are as defined in classes and subclasses herein and compositions (e.g., pharmaceutical compositions) comprising such compounds, which compounds are useful as inhibitors of hepatitis C virus polymerase, and thus are useful, for example, as medicaments for the treatment of HCV infection.

NMDA RECEPTOR MODULATORS AND USES RELATED THERETO

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Page/Page column 38, (2014/03/21)

This disclosure relates to NMDA modulators and used related thereto such as for treatment of central nervous system disorders. In certain embodiments, compounds disclosed herein are NR2C subunit-selective NMDA potentiators. In certain embodiments, the disclosure contemplates compounds and pharmaceutical compositions. In certain embodiments, the disclosure contemplates compounds disclosed herein as prodrugs, optionally substituted with one or more substituents, derivatives, or salts thereof. In certain embodiments, the disclosure relates to methods of treating or preventing nervous system disorders comprising administering an effective amount of a composition comprising compound disclosed herein to a subject in need thereof.

Design, synthesis, and structure-activity relationship of a novel series of GluN2C-selective potentiators

Zimmerman, Sommer S.,Khatri, Alpa,Garnier-Amblard, Ethel C.,Mullasseril, Praseeda,Kurtkaya, Natalie L.,Gyoneva, Stefka,Hansen, Kasper B.,Traynelis, Stephen F.,Liotta, Dennis C.

supporting information, p. 2334 - 2356 (2014/04/17)

NMDA receptors are tetrameric complexes composed of GluN1 and GluN2A-D subunits that mediate a slow Ca2+-permeable component of excitatory synaptic transmission. NMDA receptors have been implicated in a wide range of neurological diseases and thus represent an important therapeutic target. We herein describe a novel series of pyrrolidinones that selectively potentiate only NMDA receptors that contain the GluN2C subunit. The most active analogues tested were over 100-fold selective for recombinant GluN2C-containing receptors over GluN2A/B/D-containing NMDA receptors as well as AMPA and kainate receptors. This series represents the first class of allosteric potentiators that are selective for diheteromeric GluN2C-containing NMDA receptors.

Substituted tricyclic compounds with activity towards ep1 receptors

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Paragraph 0091, (2013/10/22)

The present invention belongs to the field of EP1 receptor ligands. More specifically it refers to compounds of general formula (I) having great affinity and selectivity for the EP1 receptor. The invention also refers to the process for their preparation,

SUBSTITUTED TRICYCLIC COMPOUNDS WITH ACTIVITY TOWARDS EP1 RECEPTORS

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Page/Page column 40; 41, (2013/10/22)

The present invention belongs to the field of EPl receptor ligands. More specifically it refers to compounds of general formula (I) having great affinity and selectivity for the EPl receptor. The invention also refers to the process for their preparation, to their use as medicament for the treatment and/or prophylaxis of diseases or disorders mediated by the EPl receptor as well as to pharmaceutical compositions comprising them.

SUBSTITUTED TRICYCLIC COMPOUNDS WITH ACTIVITY TOWARDS EP1 RECEPTORS

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Page/Page column 48; 49, (2013/10/22)

The present invention belongs to the field of EP1 receptor ligands. More specifically it refers to compounds of general formula (I) having great affinity and selectivity for the EP1 receptor. The invention also refers to the process for their preparation, to their use as medicament for the treatment and/or prophylaxis of diseases or disorders mediated by the EP1 receptor as well as to pharmaceutical compositions comprising them.

A concise synthesis of the pennsylvania green fluorophore and labeling of intracellular targets with O6-benzylguanine derivatives

Mottram, Laurie F.,Maddox, Ewa,Schwab, Markus,Beaufils, Florent,Peterson, Blake R.

, p. 3741 - 3744 (2008/02/12)

We report improved syntheses of the Pennsylvania Green and 4-carboxy-Pennsylvania Green fluorophores; the latter compound was prepared from methyl 4-iodo-3-methylbenzoate in a three-pot process (32% overall yield). Chinese hamster ovary cells expressing O

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