Naphtho(1,2-d)thiazolium, 1-methyl-2-(2-(2-methyl-1H-indol-3-yl)-1-propenyl)-, salt with 4-methylbenzenesulfonic acid (1:1)

Base Information

• Chemical Name: Naphtho(1,2-d)thiazolium, 1-methyl-2-(2-(2-methyl-1H-indol-3-yl)-1-propenyl)-, salt with 4-methylbenzenesulfonic acid (1:1)
• CAS No.: 62609-97-6
• Molecular Formula: C31H28N2O3S2
• Molecular Weight: 540.6956
• Mol file: 62609-97-6.mol

Synonyms:62609-97-6;1-Methyl-2-(2-(2-methyl-1H-indol-3-yl)-1-propenyl)naphtho(1,2-d)thiazolium, 4-methylbenzenesulfonic acid salt;Naphtho(1,2-d)thiazolium, 1-methyl-2-(2-(2-methyl-1H-indol-3-yl)-1-propen-1-yl)-, 4-methylbenzenesulfonate (1:1);Naphtho(1,2-d)thiazolium, 1-methyl-2-(2-(2-methyl-1H-indol-3-yl)-1-propenyl)-, salt with 4-methylbenzenesulfonic acid (1:1);Naphtho[1,2-d]thiazolium, 1-methyl-2-[2-(2-methyl-1H-indol-3-yl)-1-propenyl]-, salt with 4-methylbenzenesulfonic acid (1:1);C24H21N2S.C7H7O3S;C24-H21-N2-S.C7-H7-O3-S

Chemical Property of Naphtho(1,2-d)thiazolium, 1-methyl-2-(2-(2-methyl-1H-indol-3-yl)-1-propenyl)-, salt with 4-methylbenzenesulfonic acid (1:1)

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 108.28000
• Density: g/cm³
• LogP: 7.79240
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 540.15413511
• Heavy Atom Count: 38
• Complexity: 768

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC=C(C=C1)S(=O)(=O)[O-].CC1=C(C2=CC=CC=C2N1)C(=CC3=[N+](C4=C(S3)C=CC5=CC=CC=C54)C)C
• Isomeric SMILES: CC1=CC=C(C=C1)S(=O)(=O)[O-].CC1=C(C2=CC=CC=C2N1)/C(=C/C3=[N+](C4=C(S3)C=CC5=CC=CC=C54)C)/C

Technology Process of Naphtho(1,2-d)thiazolium, 1-methyl-2-(2-(2-methyl-1H-indol-3-yl)-1-propenyl)-, salt with 4-methylbenzenesulfonic acid (1:1)

There total 1 articles about Naphtho(1,2-d)thiazolium, 1-methyl-2-(2-(2-methyl-1H-indol-3-yl)-1-propenyl)-, salt with 4-methylbenzenesulfonic acid (1:1) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

2-methyl-1H-indole (95-20-5) + 1,2-dimethylnaphtho[1,2-d]thiazol-1-ium 4-methylbenzenesulfonate (58480-17-4) + Triethyl orthoacetate (78-39-7) → 1-methyl-2-[2-(2-methyl-indol-3-yl)-propenyl]-naphtho[1,2-d]thiazolium; toluene-4-sulfonate (62609-97-6)

Guidance literature:

upstream raw materials:

2-methyl-1H-indole

1,2-dimethylnaphtho[1,2-d]thiazol-1-ium 4-methylbenzenesulfonate

Triethyl orthoacetate