80279-71-6

Usage

Derivative of

Indole

Type of compound

Sulfonic acid

Form

Dihydro (contains two hydrogen atoms in the dihydrogenated form of the indole ring)

Physical appearance

White to off-white powder

Solubility

Soluble in water and other polar solvents

Uses

Building block in the synthesis of various pharmaceuticals and other organic compounds, potential uses in the fields of chemistry and pharmaceuticals.

Upstream product

• 496-15-1 1-indoline 

Downstream Products

• 1026285-62-0 2-[3,6-Bis-(6-dimethylsulfamoyl-2,3-dihydro-indol-1-yl)-9H-xanthen-9-yl]-benzenesulfonyl chloride 
• 1026709-94-3 2-[3,6-Bis-(6-dimethylsulfamoyl-2,3-dihydro-indol-1-yl)-9H-xanthen-9-yl]-benzenesulfonic acid 
• 313690-18-5 1-acetyl-2,3-dihydro-1H-indole-6-sulfonylchloride 

Relevant academic research and scientific papers

COMPOUNDS AND METHODS

Disclosed are compounds having the Formula (I), wherein X, Y, Z, R1, R2 and R3 are as defined herein, and methods of making and using the same.

COMPOUNDS AND METHODS

Disclosed are compounds having formula (I), wherein R1, R2, R3, R4, Z1, Z2, Z3 and Z4 are as defined herein, and methods of making and using the same.

COMPOUNDS AND METHODS

Disclosed are compounds having the formula (I): wherein R1, R2, R3, R4, R5, and R6 are as defined herein, and methods of making and using the same.

Bicyclo nitrogenheterocyclic substituted sulfofluoresceins, fluoresceins and xanthenes

There are described novel dye compounds which are represented by the formula STR1 wherein A is STR2 X is H, alkyl, aryl such as phenyl or naphthyl, or substituted aryl; W is H or alkyl; R is H or alkyl; Z and Y are each H or monovalent radicals; l and p are each 1 or 2 and m and n are each integers of from 2-6.