487-68-3 | 2,4,6-Trimethylbenzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
10g	95%	in stock	$8.00	$5.00
25g	95%	in stock	$9.00	$6.00
100g	95%	in stock	$18.00	$12.00
500g	95%	in stock	$65.00	$45.00
1kg	95%	in stock	$98.00	$68.00

Description

• Catalog Number: AB60059
• Chemical Name: 2,4,6-Trimethylbenzaldehyde
• CAS Number: 487-68-3
• Molecular Formula: C10H12O
• Molecular Weight: 148.2017
• MDL Number: MFCD00003341
• SMILES: O=Cc1c(C)cc(cc1C)C
• NSC Number: 29094

Computed Properties

• Complexity: 130
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.5

Upstream Synthesis Route

2,4,6-Trimethylbenzaldehyde, also known as mesityl aldehyde, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure consisting of three methyl groups attached to a benzene ring makes it a valuable intermediate in various synthetic pathways.One key application of 2,4,6-Trimethylbenzaldehyde is as a precursor in the synthesis of pharmaceutical compounds and fine chemicals. By undergoing different chemical reactions, such as condensation reactions and reduction reactions, it can be transformed into a wide range of derivatives with diverse functionalities. These derivatives are essential components in the creation of drugs, fragrances, and other high-value products.Moreover, 2,4,6-Trimethylbenzaldehyde is commonly used in the manufacturing of organic pigments and dyes. Its aromatic structure allows for the production of vibrant and stable colorants that find applications in various industries, including textiles, plastics, and paints.In addition, this compound serves as a building block in the synthesis of advanced materials, such as liquid crystals and polymers. Through controlled chemical modifications, researchers can tailor the properties of these materials for specific applications in electronics, optics, and coatings.Overall, the versatility of 2,4,6-Trimethylbenzaldehyde in chemical synthesis showcases its importance in producing a wide array of valuable products across different sectors. Its unique structure and reactivity make it a valuable asset for researchers and industrial chemists seeking to develop innovative compounds and materials.

Literature

• Screening of endocrine activity of compounds migrating from plastic baby bottles using a multi-receptor panel of in vitro bioassays.

  Toxicology in vitro : an international journal published in association with BIBRA 20161201

• [8-(4-Chloro-benzo-yl)-2,7-dimeth-oxy-naphthalen-1-yl](2,4,6-trimethyl-phen-yl)methanone.

  Acta crystallographica. Section E, Structure reports online 20120301

• [2,7-Dimeth-oxy-8-(2,4,6-trimethyl-benzo-yl)naphthalen-1-yl](2,4,6-trimethyl-phen-yl)methanone.

  Acta crystallographica. Section E, Structure reports online 20120101

• (E)-4-Chloro-N-(2,4,6-trimethyl-benzyl-idene)aniline.

  Acta crystallographica. Section E, Structure reports online 20110801

• N,N'-Bis[(E)-2,4,6-trimethyl-benzyl-idene]ethane-1,2-diamine.

  Acta crystallographica. Section E, Structure reports online 20110801

• A study on the essential oil of Ferulago campestris: how much does extraction method influence the oil composition?

  Journal of separation science 20110201

• Solvolyses of benzoyl chlorides in weakly nucleophilic media.

  International journal of molecular sciences 20110101

• (E)-N'-(2,4,6-Trimethyl-benzyl-idene)isonicotinohydrazide.

  Acta crystallographica. Section E, Structure reports online 20100601

• 2,6-Disubstituted benzoates as neighboring groups for enhanced diastereoselectivity in beta-galactosylation reactions: synthesis of beta-1,3-linked oligogalactosides related to arabinogalactan proteins.

  The Journal of organic chemistry 20091218

• DFT studies on the mechanism of the diboration of aldehydes catalyzed by copper(I) boryl complexes.

  Journal of the American Chemical Society 20080423

• Essential oil composition of the different parts of Eryngium corniculatum Lam. (Apiaceae) from Spain.

  Journal of chromatography. A 20071221

• Synthesis of sterically crowded derivatives of anomeric pairs of D-glucose disaccharides.

  Carbohydrate research 20050905

• Efficient photocyclization of o-alkylbenzaldehydes in the solid state: direct observation of E-xylylenols en route to benzocyclobutenols.

  The Journal of organic chemistry 20011019