19499-83-3

Usage

Uses

Used in Research and Development:
1H-Indol-4-ol, 5-methylis used as a chemical intermediate for the synthesis of more complex compounds in research and development settings. Its unique structure and reactivity make it a valuable component in the creation of new chemical entities.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1H-Indol-4-ol, 5-methylis used as a building block for the development of new drugs. Its presence in the molecular structure can contribute to the desired pharmacological properties, such as increased potency or selectivity.
Used in Chemical Synthesis:
1H-Indol-4-ol, 5-methylis employed as a key component in the synthesis of various chemical products, including dyes, pigments, and other specialty chemicals. Its versatility in reacting with other compounds allows for the creation of a wide range of products with different applications.

Upstream product

• 2380-94-1 1H-indol-4-ol 
• 50-00-0 formaldehyd 
• 19499-82-2 5-(N,N-dimethylaminomethyl)indol-4-ol 

Downstream Products

• 770250-71-0 5-methylindolin-4-ol 
• 770251-21-3 phosphoric acid 2-[4-(4-{2-[2-(1-acetyl-5-methyl-7-nitro-2,3-dihydro-1H-indol-4-yloxy)-acetylamino]-ethoxy}-benzoyl)-phenoxy]-ethyl ester di-tert-butyl ester 
• 835889-79-7 4-[(1-acetyl-5-methyl-7-nitroindolin-4-yloxy)acetamido]-4'-{2-[di(tert-butoxy)phosphoryloxy]ethoxy}benzophenone 
• 770251-13-3 4-{2-[(1-acetyl-5-methyl-7-nitroindolin-4-yloxy)acetamido]ethoxy}-4'-[2-(dihydroxyphosphoryloxy)ethoxy]benzophenone 
• 835889-78-6 phosphoric acid 2-(4-{4-[2-(1-acetyl-5-methyl-7-nitro-2,3-dihydro-1H-indol-4-yloxy)-ethoxy]-benzoyl}-phenoxy)-ethyl ester di-tert-butyl ester 

Relevant academic research and scientific papers

Optimised synthesis and photochemistry of antenna-sensitised 1-acyl-7-nitroindolines

Benzophenone antenna-sensitised 1-acyl-7-nitroindolines show a significantly enhanced extent of photochemical cleavage in aqueous solution over their non-sensitised analogues and release the carboxylate derived from their 1-acyl group. The present work in

7-NITROINDOLINE DERIVATIVES AND THEIR USES

7-nitroindoline compounds are disclosed that comprise a triplet sensitising group such as substituted or unsubstituted benzophenone group and can be used to cage effector species. In particular, the inclusion of a triplet sensitising group linked to the 4 or 5 position of a 7-nitroindoline derivative provides compounds which can be photolysed to release the effector species with unexpectedly enhanced photolysis efficiency. The triplet sensitising group may be linked directly to the 7-nitroindoline or via a spacer group. In some examples, the triplet sensitising group and/or the spacer group can be selected to enhance other properties of the caged compound such as its solubility, spectroscopic properties or stability (e.g. stability of the linkage between the nitroindoline moiety and the triplet sensitiser). This can help to improve the performance of the caged compound, especially in aqueous environments containing dissolved oxygen.

Product based on inorganic or organic lamellar particles, containing a melanotic pigment, process for preparing it and its use in cosmetics

The invention relates to a product in powder form consisting of organic or inorganic particles having a lamellar structure, having a size of less than 50 microns and containing at least one synthetic melanotic pigment formed in situ by oxidation of an indole compound, and to its use for the protection of the human epidermis, in make-up products and for dyeing hair.