N-Phenyl-2H-[1,3]dioxolo[4,5-B]acridin-10-amine

Base Information

Chemical Name:N-Phenyl-2H-[1,3]dioxolo[4,5-B]acridin-10-amine
CAS No.:141991-07-3
Molecular Formula:C₂₀H₁₄N₂O₂
Molecular Weight:314.343
Hs Code.:
DSSTox Substance ID:DTXSID30576243
Nikkaji Number:J466.146J
Wikidata:Q82465822

Synonyms:141991-07-3;N-PHENYL-2H-[1,3]DIOXOLO[4,5-B]ACRIDIN-10-AMINE;9-anilino-2,3-methylenedioxyacridine;DTXSID30576243

Suppliers and Price of N-Phenyl-2H-[1,3]dioxolo[4,5-B]acridin-10-amine

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 1 raw suppliers

Chemical Property of N-Phenyl-2H-[1,3]dioxolo[4,5-B]acridin-10-amine

Chemical Property:

XLogP3:4.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:314.105527694
Heavy Atom Count:24
Complexity:439

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1OC2=CC3=C(C4=CC=CC=C4N=C3C=C2O1)NC5=CC=CC=C5

Technology Process of N-Phenyl-2H-[1,3]dioxolo[4,5-B]acridin-10-amine

There total 4 articles about N-Phenyl-2H-[1,3]dioxolo[4,5-B]acridin-10-amine 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:

: 2591-26-6
6-chlorobenzo[1,3]dioxole-5-carboxylic acid

: 141991-07-3
9-anilino-2,3-methylenedioxyacridine

Guidance literature:: Multi-step reaction with 3 steps

1: 21 percent / K₂CO₃, copper bronze / 6 h / Heating

2: POCl₃ / 3 h / Heating

3: ethanol / 20 h / Ambient temperature

With copper; potassium carbonate; trichlorophosphate; In ethanol;
DOI:10.1002/jhet.5570290112

Reference yield:

: 141991-08-4
2-anilino-4,5-methylenedioxybenzoic acid

: 141991-07-3
9-anilino-2,3-methylenedioxyacridine

Guidance literature:: Multi-step reaction with 2 steps

1: POCl₃ / 3 h / Heating

2: ethanol / 20 h / Ambient temperature

With trichlorophosphate; In ethanol;
DOI:10.1002/jhet.5570290112

Reference yield:

: 62-53-3
aniline

: 141991-07-3
9-anilino-2,3-methylenedioxyacridine

Guidance literature:: Multi-step reaction with 3 steps

1: 21 percent / K₂CO₃, copper bronze / 6 h / Heating

2: POCl₃ / 3 h / Heating

3: ethanol / 20 h / Ambient temperature

With copper; potassium carbonate; trichlorophosphate; In ethanol;
DOI:10.1002/jhet.5570290112