2-Chlorobenzo[e][1]benzothiopyrano[4,3-b]indole

Base Information

Chemical Name:2-Chlorobenzo[e][1]benzothiopyrano[4,3-b]indole
CAS No.:32226-65-6
Molecular Formula:C₁₉H₁₀ClNS
Molecular Weight:319.814
Hs Code.:2934999090
Mol file:32226-65-6.mol

Synonyms:2-Chloro[1]benzothiopyrano[4,3-b]benzo[e]indole;2-Chlorobenzo[e] [1]benzothiopyrano[4,3-b] indole

Suppliers and Price of 2-Chlorobenzo[e][1]benzothiopyrano[4,3-b]indole

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of 2-Chlorobenzo[e][1]benzothiopyrano[4,3-b]indole

Chemical Property:

Vapor Pressure:9.21E-10mmHg at 25°C
Refractive Index:1.6000 (estimate)
Boiling Point:503.3°Cat760mmHg
Flash Point:258.2°C
PSA：41.13000
Density:1.42g/cm³
LogP:6.36090

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2-Chlorobenzo[e][1]benzothiopyrano[4,3-b]indole

There total 2 articles about 2-Chlorobenzo[e][1]benzothiopyrano[4,3-b]indole 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:

: 33834-65-0
2-chloro-6,13-dihydro-benzo[e]thiochromeno[4,3-b]indole

: 32226-65-6
2-chloro-benzo[e]thiochromeno[4,3-b]indole

Guidance literature:: With 2,4,6-Trinitrophenol; In ethanol;
DOI:10.1039/P19720001266

Reference yield:

: 6-chloro-thiochroman-4-one naphthalen-2-ylhydrazone

: 32226-65-6
2-chloro-benzo[e]thiochromeno[4,3-b]indole

Guidance literature:: Multi-step reaction with 2 steps

1: HCl / acetic acid

2: picric acid / ethanol

With hydrogenchloride; 2,4,6-Trinitrophenol; In ethanol; acetic acid;
DOI:10.1039/P19720001266