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Methyl 4-acetyl-2-Methylbenzoate, also known as 4-acetyl-2-Methylbenzoic acid methyl ester, is a chemical compound belonging to the class of organic compounds known as benzoyl esters. It features a benzene ring with a methyl group and an acetyl group attached at specific positions, which allows for a wide range of potential reactions and applications. Methyl 4-acetyl-2-Methylbenzoate is characterized by a strong odor and is flammable, necessitating careful handling.

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  • 1036715-60-2 Structure
  • Basic information

    1. Product Name: Methyl 4-acetyl-2-Methylbenzoate
    2. Synonyms: Methyl 4-acetyl-2-Methylbenzoate
    3. CAS NO:1036715-60-2
    4. Molecular Formula: C11H12O3
    5. Molecular Weight: 192.21118
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 1036715-60-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Methyl 4-acetyl-2-Methylbenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 4-acetyl-2-Methylbenzoate(1036715-60-2)
    11. EPA Substance Registry System: Methyl 4-acetyl-2-Methylbenzoate(1036715-60-2)
  • 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: 1036715-60-2(Hazardous Substances Data)

1036715-60-2 Usage

Uses

Used in Flavor and Fragrance Industry:
Methyl 4-acetyl-2-Methylbenzoate is used as a flavoring agent and fragrance ingredient for its distinctive aromatic properties, enhancing the sensory experience of various products.
Used in Pharmaceutical Synthesis:
As an intermediate in the synthesis of pharmaceuticals, Methyl 4-acetyl-2-Methylbenzoate plays a crucial role in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Cosmetics and Personal Care Products:
Methyl 4-acetyl-2-Methylbenzoate is utilized in the production of cosmetics and personal care products, where it may serve as a scent component or contribute to the formulation's overall effectiveness.
Used in Industrial Processes:
Methyl 4-acetyl-2-Methylbenzoate is also employed in various industrial processes, where its chemical properties can be harnessed for specific applications, such as in the manufacturing of certain types of plastics or other materials.

Check Digit Verification of cas no

The CAS Registry Mumber 1036715-60-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,7,1 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1036715-60:
(9*1)+(8*0)+(7*3)+(6*6)+(5*7)+(4*1)+(3*5)+(2*6)+(1*0)=132
132 % 10 = 2
So 1036715-60-2 is a valid CAS Registry Number.

1036715-60-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-acetyl-2-methylbenzoate

1.2 Other means of identification

Product number -
Other names Methyl 4-acetyl-2-Methylbenzoate

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:1036715-60-2 SDS

1036715-60-2Relevant articles and documents

Catalytic Enantioselective Direct Aldol Addition of Aryl Ketones to α-Fluorinated Ketones

Barber, David M.,Dixon, Darren J.,Thomson, Connor J.

supporting information, p. 5359 - 5364 (2020/02/28)

The catalytic enantioselective synthesis of α-fluorinated chiral tertiary alcohols from (hetero)aryl methyl ketones is described. The use of a bifunctional iminophosphorane (BIMP) superbase was found to facilitate direct aldol addition by providing the strong Br?nsted basicity required for rapid aryl enolate formation. The new synthetic protocol is easy to perform and tolerates a broad range of functionalities and heterocycles with high enantioselectivity (up to >99:1 e.r.). Multi-gram scalability has been demonstrated along with catalyst recovery and recycling. 1H NMR studies identified a 1400-fold rate enhancement under BIMP catalysis, compared to the prior state-of-the-art catalytic system. The utility of the aldol products has been highlighted with the synthesis of various enantioenriched building blocks and heterocycles, including 1,3-aminoalcohol, 1,3-diol, oxetane, and isoxazoline derivatives.

Method for synthesizing methyl 2-methyl-4-acetyl benzoate

-

, (2019/04/18)

The invention provides a method for synthesizing methyl 2-methyl-4-acetyl benzoate. The method comprises the following steps: (1) adding an acylating reagent to a solution with dissolved 2-fluorotoluene, and carrying out an acylation reaction so as to obtain 4-fluoro-3-methylacetophenone; (2) dissolving the obtained 4-fluoro-3-methylacetophenone, adding a cyanation reagent, and carrying out a cyanation reaction so as to obtain 3-methyl-4-cyanoacetophenone; (3) adding acid to the 3-methyl-4-cyanoacetophenone, and carrying out a hydrolysis reaction so as to obtain 2-methyl-4-acetylbenzoic acid;and (4) adding methanol to the 2-methyl-4-acetylbenzoic acid, and carrying out an esterification reaction so as to obtain methyl 2-methyl-4-acetyl benzoate. The method has simple operation, a high reaction yield, easily purchasable reagents and instruments and low cost, and is feasible in specific practical application.

SUBSTITUTED BENZENE AND 6,5-FUSED BICYCLIC HETEROARYL COMPOUNDS

-

, (2016/05/02)

The present invention relates to substituted benzene compounds and bicyclic heteroaryl compounds. The present invention also relates to pharmaceutical compositions containing these compounds and methods of treating cancer by administering these compounds and pharmaceutical compositions to subjects in need thereof. The present invention also relates to the use of such compounds for research or other non-therapeutic purposes.

Modulators of methyl modifying enzymes, compositions and uses thereof

-

Page/Page column 225; 226, (2015/12/26)

Agents for modulating methyl modifying enzymes, compositions and uses thereof are provided herein.

MODULATORS OF METHYL MODIFYING ENZYMES, COMPOSITIONS AND USES THEREOF

-

Paragraph 00492; 00495, (2013/06/05)

Agents for modulating methyl modifying enzymes, compositions and uses thereof are provided herein

Synthesis and antimicrobial screening of some novel pyrazoline derivatives

Kundariya,Rupala,Patel

experimental part, p. 2045 - 2048 (2012/08/07)

New series of methyl-4-(4,5-dihydro-5-[(Z)phenyl]-1H-pyrazol-3-yl)-2- methylbenzohydrazide were synthesized by cyclisization of chalcones, methyl 4-((E)-3-((Z)phenyl)acryloyl)-2-methylbenzoate with hydrazine hydrate in presence of basic media. The chalcon

Selective oxidation of acetophenones bearing various functional groups to benzoic acid derivatives with molecular oxygen

Nakamura, Ryota,Obora, Yasushi,Ishii, Yasutaka

experimental part, p. 1677 - 1684 (2011/02/25)

Acetophenones substituted by alkyl, alkoxy, acetoxy, and halogen groups were selectively oxidized with molecular oxygen to the corresponding benzoic acids by using the N,N',N"-trihydroxyisocyanuric acid (THICA)/cobalt(II) acetate [Co(OAc)2] and THICA/Co(OAc)2/manganese(II) acetate.

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