2-nitro-1H-indene

Base Information

Chemical Name:2-nitro-1H-indene
CAS No.:16021-01-5
Molecular Formula:C9H7NO2
Molecular Weight:161.16
Hs Code.:
DSSTox Substance ID:DTXSID10456094
Nikkaji Number:J680.606F
Wikidata:Q82278307
Mol file:16021-01-5.mol

Synonyms:2-nitro-1H-indene;16021-01-5;1H-Indene, 2-nitro-;SCHEMBL16033451;DTXSID10456094

Suppliers and Price of 2-nitro-1H-indene

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 6 raw suppliers

Chemical Property of 2-nitro-1H-indene

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:161.047678466
Heavy Atom Count:12
Complexity:229

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C2=CC=CC=C2C=C1[N+](=O)[O-]

Technology Process of 2-nitro-1H-indene

There total 1 articles about 2-nitro-1H-indene 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: 20.0%

: 609-40-5
2-nitrothiophene

: 95-13-6
1-indene

: 16021-01-5
2-nitro-indene

: 63440-60-8
2-(o-tolyl)-2-oxo-ethanale

: 615-13-4
2-indanone

: 150994-10-8
2-(2-thienyl)indene

Guidance literature:: In acetonitrile; for 1h;
DOI:10.1016/0040-4020(96)00878-2

Reference yield:

: 16021-01-5
2-nitro-indene

: 615-13-4
2-indanone

Guidance literature:: With acetic acid; zinc; man destilliert das ausgeaetherte Reduktionsprodukt mit verd. Schwefelsaeure;

Reference yield:

: 16021-01-5
2-nitro-indene

: 14563-24-7
1,2-Indandiamin

Guidance literature:: Multi-step reaction with 2 steps

1: NaHCO₃ / tetrahydrofuran / Ambient temperature

2: H₂ / 10percent Pd/C / ethanol / 760 Torr / Ambient temperature

With hydrogen; sodium hydrogencarbonate; palladium on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1246/cl.1996.291