113995-55-4

Usage

Uses

Used in Organic Chemistry:
1,1,2-Trimethyl-1H-benz[e]indole-7-sulfonic acid is used as a building block for the synthesis of more complex organic molecules, leveraging its unique structure to create a variety of compounds with different properties and applications.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 1,1,2-Trimethyl-1H-benz[e]indole-7-sulfonic acid is used as a precursor for the development of new pharmaceutical drugs. Its potential role in drug discovery is attributed to its chemical properties, which may contribute to the creation of novel therapeutic agents.
Used in Aqueous Environments:
Due to its water-soluble properties conferred by the sulfonic acid group, 1,1,2-Trimethyl-1H-benz[e]indole-7-sulfonic acid is suitable for use in aqueous environments, which can be beneficial for applications requiring solubility in water, such as in certain chemical processes or reactions.
Further research and study into the properties and potential applications of 1,1,2-Trimethyl-1H-benz[e]indole-7-sulfonic acid are ongoing, indicating that its uses may expand as new insights and discoveries are made in the fields of chemistry and medicine.

Upstream product

• 41532-84-7 2,3,3-trimethylbenzo[e]indole 

Relevant academic research and scientific papers

NOVEL ORGANIC COMPOUND, NEAR-INFRARED FLUORESCENT CONSTANT MEDIUM CONTAINING SAME, AND METHOD FOR NANO-GRANULATING CONSTANT MEDIUM

The present invention relates to a novel organic compound, a near-infrared fluorescent constant medium containing the same, and a method for nano-granulating the constant medium.

Rigidized trimethine cyanine dyes

Disclosed are analogues of trimethine cyanine dyes which are useful for imparting fluorescent properties to target materials by covalent and non-covalent association. The compounds have general formula (2) optionally substituted by groups R2-R9wherein groups R6, R7, R8and R9are attached to the rings containing X and Y or, optionally are attached to atoms of the Zaand Zbring structures and groups R1-R9are chosen to provide desired solubility, reactivity and spectralproperties to the fluorescent compounds; A is selected from O, S and NR11where R11is the substituted amino radical (a), where R′ is selected from hydrogen, a C1-4alkyl and aryl and R″ is selected from C1-18alkyl, aryl, heteroaryl, an acyl radical having from 2-7 carbon atoms, and a thiocarbamoyl radical; Zaand Zbeach represent a bond or the atoms necessary to complete one, two fused or three fused aromatic rings each ring having five or six atoms, selected from carbon atoms and, optionally, non more than two oxygen, nitrogen and sulphur atoms.

Rigidized trimethine cyanine dyes

Disclosed are analogues of trimethine cyanine dyes which are useful for imparting fluorescent properties to target materials by covalent and non-covalent association. The compounds have the following general formula: optionally substituted by groups R2-R9 wherein groups R6, R7, R8 and R9 are attached to the rings containing X and Y or, optionally are attached to atoms of the Za and Zb ring structures and groups R1-R9 are chosen to provide desired solubility, reactivity and spectral properties to the fluorescent compounds; A is selected from O, S and NR11 where R11 is the substituted amino radical: where R′ is selected from hydrogen, a C1-4 alkyl and aryl and R″ is selected from C1-18 alkyl, aryl, heteroaryl, an acyl radical having from 2-7 carbon atoms, and a thiocarbamoyl radical; Za and Zb each represent a bond or the atoms necessary to complete one, two fused or three fused aromatic rings each ring having five or six atoms, selected from carbon atoms and, optionally, no more than two oxygen, nitrogen and sulphur atoms.

Novel infrared absorbing dyes and photographic elements containing same

A compound, useful as an infrared absorbing dye, having the structure: is disclosed for use in photographic elements. In this formula, R1 and R2 each independently represents sulfoalkyl, carboxyalkyl, or sulfatoalkyl of from 3 to 6 carbon atoms, having at least 3 carbon atoms in the alkyl chain between the nitrogen atom of each Z ring and the sulfo or sulfato group, and at least 2 carbon atoms in the alkyl chain between the nitrogen atom of each Z ring and the carboxy group., R3 and R5 are each hydrogen or together represent the atoms necessary to complete 5- or 6-membered carbocyclic ring, and R4 represents hydrogen, alkyl of 1 to 4 carbon atoms, aryl, cyano, halogen, or , where R6 and R7 each independently represents alkyl of from 1 to 6 carbon atoms or aryl, or together represent the non-metallic atoms necessary to form a 5- or 6-membered ring., X⊕ represents a cation., Z1 and Z2 each independently represent the atoms needed to complete an indole, naphthindole or benzindole nucleus