Sodium 1-acetylindoline-2-sulfonate

Base Information

Chemical Name:Sodium 1-acetylindoline-2-sulfonate
CAS No.:26807-69-2
Molecular Formula:C10H11NO4S.Na
Molecular Weight:263.249
Hs Code.:
DSSTox Substance ID:DTXSID90369456
Mol file:26807-69-2.mol

Synonyms:sodium 1-acetylindoline-2-sulfonate;26807-69-2;sodium;1-acetyl-2,3-dihydroindole-2-sulfonate;sodium 1-acetyl-2,3-dihydro-1H-indole-2-sulfonate;DTXSID90369456;CCG-42633;AKOS015955298;AKOS015966311;FT-0674613;J-016556;SR-01000632615-1

Suppliers and Price of Sodium 1-acetylindoline-2-sulfonate

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

Usbiological
Sodium 1-Acetylindoline-2-sulfonate
1g
$ 446.00

TRC
Sodium1-Acetylindoline-2-sulfonate
500mg
$ 90.00

Medical Isotopes, Inc.
Sodium1-Acetylindoline-2-sulfonate
25 g
$ 1800.00

Medical Isotopes, Inc.
Sodium1-Acetylindoline-2-sulfonate
5 g
$ 850.00

aablocks
Sodium1-Acetylindoline-2-sulfonate
25g
$ 2300.00

aablocks
Sodium1-Acetylindoline-2-sulfonate
5g
$ 1113.00

Total 5 raw suppliers

Chemical Property of Sodium 1-acetylindoline-2-sulfonate

Chemical Property:

Melting Point:>300°C
PSA：85.89000
LogP:1.61270
Solubility.:Water
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:263.02282326
Heavy Atom Count:17
Complexity:392

Purity/Quality:

98% ^*data from raw suppliers

Sodium 1-Acetylindoline-2-sulfonate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)N1C(CC2=CC=CC=C21)S(=O)(=O)[O-].[Na+]
Uses Sodium 1-Acetylindoline-2-sulfonate (cas# 26807-69-2) is a compound useful in organic synthesis.

Technology Process of Sodium 1-acetylindoline-2-sulfonate

There total 2 articles about Sodium 1-acetylindoline-2-sulfonate 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: 90.0%

: 26807-68-1
indolin-2-sulfonic acid sodium

: 108-24-7
acetic anhydride

: 26807-69-2
N-acetylindololine-2-sulfonic acid sodium

Guidance literature:: at 70 - 90 ℃; for 2.5h; Inert atmosphere;

Reference yield:

: 120-72-9
indole

: 26807-69-2
N-acetylindololine-2-sulfonic acid sodium

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydrogensulfite / ethanol; water / 20 h / 20 °C

2: 2.5 h / 70 - 90 °C

With sodium hydrogensulfite; In ethanol; water;
DOI:10.1016/j.bmc.2012.01.031

Reference yield: 92.0%

: 26807-69-2
N-acetylindololine-2-sulfonic acid sodium

: 10075-50-0
5-bromo-1H-indole

Guidance literature:: N-acetylindololine-2-sulfonic acid sodium; With bromine; In water; at 0 - 20 ℃; for 2h;

With sodium hydroxide; In water; for 20h; Reflux;
DOI:10.1016/j.bmc.2012.01.031