Synthetic Route of 50292-95-0, In heterogeneous catalysis, the catalyst is in a different phase from the reactants. At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 50292-95-0, name is 3,3-Bis(2-methyl-1-octyl-1H-indol-3-yl)isobenzofuran-1(3H)-one. In an article，Which mentioned a new discovery about 50292-95-0
Disclosed are triarylmethane dyes of formula (1) D1 – (Z1J)r – Y1-S-A, wherein A is hydrogen; a radical of formula (1b) *- S-Y2 – (Z2)- D2; or a radical of formula (1c) *- S-Y3 ;Y1 and Y2 independently from each other are unsubstituted or substituted, straight-chain or branched, interrupted or uninterrupted C1-C10alkylene ; C5-C10cycloalkylene; C5-C10arylene ; or-C5-C10arylene-(C1-C10alkylene) ; Y3 is an unsubstituted or substituted, straight-chain or branched, interrupted or uninterrupted C1C10alkyl; C5-C10cycloalkyl; C5-C10aryl; or-C5-C10aryl-(C1-C10alkyl); Z1 and Z2 independently from each other are *-(CH2)p-C(O)-**; *-(CH2CH2-O)s-**; *-(CH2)p-C(O)O-**; *-(CH2)p-OCO-**; -(CH2)P-N(R1)-**; -(CH2)P-CON(R1)-**; -(CH2)P-(R1)NC(O)-**; -0-; -S-; -S(O)-; -S(O)2-; or a cationic biradical of a substituted or unsubstituted aromatic or heteroaromatic compound of the formula (1a); (1b); (1c); (1d); or (1e); wherein the asterix * indicates the linkage to D1 and/or D2; the asterix ** indicates the linkage to Y1 and/or Y2 ; W1 is N or a radical of CR5; R1, R2, R3, R4 and R5 independently from each other are hydrogen; C1-C14alkyl; C2- C14alkenyl; C5-C10aryl; C5-C10aryl-(C1-C10alkyl); or -C1-C10alkyl(C5-C10aryl); D1 and D2 independently from each other are hydrogen; or the residue of an organic dye selected from the radical of formula (1f), wherein B1 and B2, independently from each other are C6-C10aryl; or a 5-7-membered heterocyclic compound, which may be substituted by C1-C12alkyl, C1C12alkoxy, phenyl, hydroxy, halogen, sulfonic acid, carboxylate, or by the radical -NR6Rz or -OR6; B3 is C6-C10arylene, or a bivalent radical of a 5-7-membered heterocyclic compound, which may be substituted by C1-C12alkyl, C1-C12alkoxy, phenyl, hydroxy, halogen, sulfonic acid, carboxylate, or by the radical -NR6R7 or -OR6; R6 and R7 idependently from each other are hydrogen; or C1-C12alkyl, which may be substituted by hydroxy or C6-C10aryl; or R6 and R7 together with the linking nitrogen atom form a 5 to 7 membered heterocyclic ring; or R6 and R7 together with the linking nitrogen atom form a piperidine ring of formula (1b)* 1H ** . wherein the asterix(*) is directed to Z1 or Z2 respectively; and the asterix(**) is directed to the linking nitrogen atom; wherein one of D1 and D2 is not hydrogen; An is an anion; p is a number from O to 5; r is O or 1 ; and s is a number from 1 to 5. The compounds are useful for the dyeing of organic materials, such as keratin fibers, preferably human hair.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.50292-95-0. In my other articles, you can also check out more blogs about 50292-95-0
Reference：
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles