21528-31-4

Usage

Uses

Used in Organic Synthesis:
2-[4-(dimethylamino)benzoyl]benzoic acid is utilized as a reagent in organic chemistry reactions, facilitating the synthesis of a wide range of compounds. Its presence in these reactions is crucial for the formation of desired products, making it an indispensable component in the field of organic synthesis.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-[4-(dimethylamino)benzoyl]benzoic acid serves as a building block for the synthesis of various pharmaceutical compounds. Its unique structure and properties contribute to the development of new drugs with potential therapeutic applications.
Used in Material Science:
2-[4-(dimethylamino)benzoyl]benzoic acid is also employed in material science for the development of novel materials with specific properties. Its incorporation into these materials can enhance their performance, making it a valuable component in the advancement of material science.
Overall, the diverse applications of 2-[4-(dimethylamino)benzoyl]benzoic acid highlight its significance in various scientific disciplines, making it a valuable chemical for research and development.

InChI:InChI=1/C16H15NO3/c1-17(2)12-9-7-11(8-10-12)15(18)13-5-3-4-6-14(13)16(19)20/h3-10H,1-2H3,(H,19,20)

Upstream product

• 121-69-7 N,N-dimethyl-aniline 
• 85-44-9 phthalic anhydride 
• 7446-70-0 aluminium trichloride 
• 7664-93-9 sulfuric acid 
• 861326-54-7 2-[3-(4-dimethylamino-phenyl)-1-oxo-inden-2-yl]-benzaldehyde 
• 7722-84-1 dihydrogen peroxide 
• 643-79-8 o-phthalic dicarboxaldehyde 
• 5339-80-0 3,3-bis-p-dimethylaminophenylphthalide  
• 100-05-0 4-nitrobenzenediazonium chloride 

Downstream Products

• 68854-19-3 2-(4-dimethylamino-benzoyl)-benzoic acid methyl ester 
• 85-44-9 phthalic anhydride 
• 62633-13-0 3-(4-dimethylaminophenyl)-1,3-dihydro-isobenzofuran-1-one 
• 75884-69-4 4-(4-dimethylamino-phenyl)-2H-phthalazin-1-one 
• 530-44-9 4-(Dimethylamino)benzophenone 
• 62930-18-1 3-(4-dimethylamino-phenyl)-3-methoxy-phthalide 
• 118202-91-8 (4-(dimethylamino)phenyl)(2-hydroxyphenyl)methanone 
• 857005-73-3 2-(4-dimethylamino-benzyl)-benzoic acid 
• 746608-53-7 2-(4-dimethylamino-3-nitro-benzoyl)-benzoic acid 
• 5339-80-0 3,3-bis-p-dimethylaminophenylphthalide  
• 6310-69-6 3-(2,4-dihydroxy-phenyl)-3-(4-dimethylamino-phenyl)-phthalide 
• 3159-92-0 3-(4-dimethylamino-phenyl)-3-(4-hydroxy-phenyl)-phthalide 
• 67699-14-3 3-[4-(dimethylamino)phenyl]-3-[N-(4-dimethylaminophenyl)-N-(4-dimethylamino)phenylamino]phthalide 
• 1028367-90-9 C₁₇H₁₇NO₂ 

Relevant academic research and scientific papers

Visible responses under high pressure in crystals: phenolphthalein and its analogues with adjustable ring-opening threshold pressures

The ring-opening reaction of phenolphthalein (PP) crystals under hydrostatic pressure provided by using a diamond anvil cell (DAC) is described in this paper for the first time. The color of the crystals changed into red from colorless visibly. The ring-opening threshold pressures could be adjusted by changing the substituent groups. Mechanochromic responses under hydrostatic pressure could also be achieved in polymer blends, which contributes to their practical applications.

OLIGOMERIC AMINOKETONES AND THEIR USE AS PHOTOINITIATORS

The invention relates to photoactive oligomeric aminoketones of general Formulae I and II, for compositions and inks curable with ultraviolet (UV) light. The oligomeric aminoketones of the general Formula I are made by condensation of aminoketones with aldehydes, and aminoketones of the general Formula II are made by acylation of aromatic amines with phthalic anhydride, followed by esterification with a polyol. The aminoketones provide good curability of energy curable coatings and inks with UV-A light, and are proposed for photoinitiator systems for low migration inks.

Phthalide compounds, and recording materials using the compounds

The invention relates to a phthalide compound of general formula (I), processes for its production, and recording materials utilizing the compound. (wherein R1 and R3 independently represent an alkyl group, a cycloalkyl group or an aralkyl group; R2 and R4 independently represent methyl or phenyl; R5 and R6 independently represent an alkyl group, a cycloalkyl group, an aralkyl group or an aryl group; R7 represents hydrogen, an alkyl group, an alkoxy group or a cyclo-alkoxy group; R5 and R6 may, taken together with the adjacent nitrogen atom, form a heterocyclic group). Recording materials utilizing the phthalide compound of the invention are suited for reading with any OCR equipped with a light source having an emission wavelength within the range of 570-780 nm.