38289-46-2

Usage

Uses

Used in Detergent Industry:
4-N-NONYLBENZOIC ACID is used as a bleaching agent for detergents, enhancing the cleaning power and whitening effect of the product. Its ability to retain perfume fragrance makes it a preferred choice for creating detergents with a pleasant scent that lasts longer.
Used in Perfumery:
In the perfume industry, 4-N-NONYLBENZOIC ACID is utilized as a fixative agent to prolong the longevity of fragrances in perfumes and other scented products. Its capacity to retain the scent of perfumes makes it an essential component in the formulation of long-lasting fragrances.
Used in Cosmetics:
4-N-NONYLBENZOIC ACID is also employed in the cosmetics industry, where it serves as an ingredient in various cosmetic products. Its fragrance retention properties contribute to the pleasant scent of these products, while its compatibility with other ingredients makes it a versatile component in the formulation of cosmetics.

InChI:InChI=1/C16H24O2/c1-2-3-4-5-6-7-8-9-14-10-12-15(13-11-14)16(17)18/h10-13H,2-9H2,1H3,(H,17,18)

Upstream product

• 463-72-9 carbamic chloride 
• 1081-77-2 n-nonylbenzene 
• 844656-92-4 4-nonylbenzoic acid methyl ester 
• 827028-03-5 methyl 4-(non-1-yn-1-yl)benzoate 
• 619-44-3 methyl 4-iodobenzoate 
• 619-58-9 4-iodobenzoic acid 
• 500-05-0 2H-pyran-2-one-5-carboxylic acid 
• 821-95-4 1-undecene 
• 586-76-5 4-Bromobenzoic acid 
• 39691-62-8 nonylmagnesium bromide 
• 70972-98-4 4-(n-nonyl)benzaldehyde 
• 41297-16-9 4-oxo-4-(4-nonyl-phenyl)-trans-crotonic acid 

Downstream Products

• 748733-78-0 4-nonylbenzamide 
• 1537168-38-9 2-{1-[4-methyl-2-(4-nonylphenyl)thiazol-5-yl]ethylidene}hydrazinecarboximidamide 
• 1537168-63-0 1-[4-methyl-2-(4-nonylphenyl)thiazol-5-yl]ethanone 
• 1537168-51-6 4-nonylthiobenzamide 
• 1566612-83-6 2-hydroxy-N'-(4'-nonylbenzoyl)benzohydrazide 
• 1566612-88-1 bis[2-(2'-hydroxyphenyl)-5-(4''-nonylphenyl)-1,3,4-oxadiazolato]beryllium(II) 
• 1384856-31-8 2-[5-(4'-nonylphenyl)-1,3,4-oxadiazol-2-yl]phenol 
• 1291073-96-5 C₅₃H₅₇NO₈ 
• 62640-25-9 p-nonylbenzyl chloride 
• 475209-02-0 p-nonylbenzyl alcohol 
• 54963-70-1 4-Nonylbenzoesaeurechlorid 
• 103176-00-7 4-Nonyl-N-[3-(1H-tetrazol-5-yl)-2,3-dihydro-benzo[1,4]dioxin-5-yl]-benzamide 
• 103177-42-0 8-(p-nonylbenzoyl)amino-2-(5-tetrazolyl)-4-oxo-4H-1-benzopyran 

Relevant academic research and scientific papers

Potentiation of the fosmidomycin analogue FR 900098 with substituted 2-oxazolines against Francisella novicida

A library of 33 compounds was screened for potentiation of the antibiotic FR 900098 against the Francisella tularensis surrogate Francisella novicida. From the screen a highly potent 2-oxazoline adjuvant was discovered capable of potentiating FR 900098 with a 1000-fold reduction in MIC against the Francisella sub-species F. novicida and F. philomiragia.

Aromatics from pyrones: Para-substituted alkyl benzoates from alkenes, coumalic acid and methyl coumalate

The Diels-Alder reaction of coumalic acid and methyl coumalate with unactivated alkenes provides only para-substituted adducts in good yield.

Palladium catalyzed cross-coupling reaction of Grignard reagents with halobenzoic acids, halophenols and haloanilines

Convenient syntheses of substituted benzoic acids, phenols and anilines have been achieved by using palladium catalyzed cross-coupling reactions between Grignard reagents and aryl halides containing carboxy, hydroxy and amino groups without a protection-deprotection sequence.

New potent antagonists of leukotrienes C4 and D4. 1. Synthesis and structure-activity relationships

(p-Amylcinnamoyl)anthranilic acid (3a) had moderate antagonist activities against LTD4-induced smooth muscle contraction on guinea pig ileum and LTC4-induced bronchoconstriction in anesthetized guinea pigs. Modifications were made in the hydrophobic part (cinnamoyl moiety) and the hydrophilic part (anthranilate moiety) of 3a. A series of 8-(benzoylamino)-2-tetrazol-5-yl-1,4-benzodioxans and 8-(benzoylamino)-2-tetrazol-5-yl-4-oxo-4H-1-benzopyrans were revealed to be potent antagonists of leukotrienes C4 and D4. Among both series, ONO-RS-347 (18k) and ONO-RS411 (19h) were the most potent and orally active antagonists, respectively. Structure-activity relationships are discussed.