5-nitroso-1H-indeno[1,2-b]pyridine

Base Information

Chemical Name:5-nitroso-1H-indeno[1,2-b]pyridine
CAS No.:65939-03-9
Molecular Formula:C₁₂H₈N₂O
Molecular Weight:196.208
Hs Code.:
DSSTox Substance ID:DTXSID40350031
Wikidata:Q82125729
Mol file:65939-03-9.mol

Synonyms:5-nitroso-1H-indeno[1,2-b]pyridine;65939-03-9;5-(hydroxyimino)indeno[3,2-b]pyridine;5H-indeno[1,2-b]pyridin-5-one oxime;Oprea1_302277;DTXSID40350031;AKOS001685695;AKOS015991641;PD127978;PD130494;10E-046;SR-01000530935;SR-01000530935-1;N-[(5E)-5H-indeno[1,2-b]pyridin-5-ylidene]hydroxylamine;N-[(5Z)-5H-INDENO[1,2-B]PYRIDIN-5-YLIDENE]HYDROXYLAMINE

Suppliers and Price of 5-nitroso-1H-indeno[1,2-b]pyridine

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

American Custom Chemicals Corporation
5H-INDENO[1,2-B]PYRIDIN-5-ONE OXIME 95.00%
5MG
$ 697.51

American Custom Chemicals Corporation
5H-INDENO[1,2-B]PYRIDIN-5-ONE OXIME 95.00%
10MG
$ 692.49

American Custom Chemicals Corporation
5H-INDENO[1,2-B]PYRIDIN-5-ONE OXIME 95.00%
1MG
$ 658.53

Total 1 raw suppliers

Chemical Property of 5-nitroso-1H-indeno[1,2-b]pyridine

Chemical Property:

PSA：45.22000
LogP:3.71900
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:196.063662883
Heavy Atom Count:15
Complexity:256

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

5H-INDENO[1,2-B]PYRIDIN-5-ONE OXIME 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C3C(=CC=CN3)C(=C2C=C1)N=O

Technology Process of 5-nitroso-1H-indeno[1,2-b]pyridine

There total 2 articles about 5-nitroso-1H-indeno[1,2-b]pyridine 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: 86.0%

: 3882-46-0
5H-indeno[1,2-b]pyridin-5-one

: 65939-03-9
4-Azafluorenone oxime

Guidance literature:: With hydroxylamine hydrochloride; In pyridine; for 10h; Heating;
DOI:10.1007/BF00506108

Reference yield:

: 65939-03-9
4-Azafluorenone oxime

Guidance literature:: entspr. Keton, NH2OH;

Reference yield:

: 65939-03-9
4-Azafluorenone oxime

: 87166-01-6
9-(p-Tolylcarbamoylamino)-4-azafluorene

Guidance literature:: Multi-step reaction with 2 steps

1: NH_2.NH₂*H₂O / Ra-Ni / ethanol / 5 h

2: ethanol

With hydrazine hydrate; Ra-Ni; In ethanol;
DOI:10.1007/BF00506108