107600-25-9

Usage

Uses

Used in Dye Manufacturing:
5-[(dimethylamino)methyl]-2-methylaniline is used as a chemical intermediate for the production of dyes. Its ability to react with other chemicals enables the creation of a wide range of dye colors and properties.
Used in Pigment Production:
In the pigment industry, 5-[(dimethylamino)methyl]-2-methylaniline serves as a key component in the synthesis of various pigments. Its chemical reactivity contributes to the development of pigments with different shades and characteristics.
Used in Pharmaceutical Development:
5-[(dimethylamino)methyl]-2-methylaniline is utilized as a building block in the synthesis of pharmaceutical compounds. Its structural complexity allows for the creation of new drug molecules with potential therapeutic applications.
Used in Chemical Research:
5-[(dimethylamino)methyl]-2-methylaniline is employed as a research compound in the field of organic chemistry. Its unique structure and reactivity make it an interesting subject for studying chemical reactions and exploring new synthetic pathways.

Upstream product

• 76765-68-9 N,N-dimethyl-3-amino-4-methylbenzamide 
• 107600-24-8 N,N-dimethyl-3-nitro-4-methylbenzamide 

Downstream Products

• 1059733-29-7 N-{5-[(dimethylamino)methyl]-2-methylphenyl}-4-[(4-pyridin-2-ylquinazolin-2-yl)amino]benzamide 
• 107600-22-6 N,N-dimethyl-3-cyano-4-methylbenzylamine 

Relevant academic research and scientific papers

AMINE COMPOUNDS

The present invention provide a compound of the formula:wherein ring A represents an aromatic ring optionally having substituents; B, Y and Ya are the same or different and each represents a bond, etc.; R1 and R2 are the same or different and each represents a hydrogen atom, etc.; R3 represents a hydrogen atom, etc.; R4 and R5 are the same or different and each represents a hydrogen, etc.; R6 represents an indolyl group optionally having substituents; and Z and Za are the same or different and each represents a hydrogen atom, etc.; or a salt thereof or a prodrug thereof, having a somatostatin receptor binding inhibition activity and is useful for preventing and/or treating diseases associated with somatostatin.

Rearrangement of (Substituted benzyl)trimethylammonium Ylides in a Nonbasic Medium: The Improved Sommelet-Hauser Rearrangement

Benzyl quaternary ammonium ylide formation in a nonbasic medium was accomplished by fluoride anion induced desilylation of benzyldimethylammonium bromide (3a) and ortho- or para-substituted benzyl analogues 3b-k.Treatment of 3 with CsF in HMPA at room temperature gives high yields of the Sommelet-Hauser rearrangement products 7 from 3a and methyl-, acetoxy-, and chloro-substituted analogues 3b-f.However, formation of the Stevens rearrangement products 8 is competitive for the reaction of compounds 3g-k having strong electron-withdrawing substituents such as acetyl, cyano, and nitrogen groups.From the o-cyano-substituted analogue 3h, a considerable amount of para Sommelet-Hauser rearrangement product is isolated.