N-[(E)-1,3-benzodioxol-5-ylmethyleneamino]-6-methyl-[1,3]dioxolo[4,5-g]quinolin-8-amine

Base Information

Chemical Name:N-[(E)-1,3-benzodioxol-5-ylmethyleneamino]-6-methyl-[1,3]dioxolo[4,5-g]quinolin-8-amine
CAS No.:91919-02-7
Molecular Formula:C₁₉H₁₅N₃O₄
Molecular Weight:349.346
Hs Code.:
NSC Number:332389
DSSTox Substance ID:DTXSID20429774
ChEMBL ID:CHEMBL563444

Synonyms:NSC332389;91919-02-7;CHEMBL563444;SCHEMBL15171169;US9624235, Compound 3;DTXSID20429774;BDBM318445;NSC-332389;1,3-Benzodioxole-5-carboxaldehyde, (6-methyl-1,3-dioxolo[4,5-g]quinolin-8-yl)hydrazone;N-[(E)-1,3-benzodioxol-5-ylmethyleneamino]-6-methyl-[1,3]dioxolo[4,5-g]quinolin-8-amine

Suppliers and Price of N-[(E)-1,3-benzodioxol-5-ylmethyleneamino]-6-methyl-[1,3]dioxolo[4,5-g]quinolin-8-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 2 raw suppliers

Chemical Property of N-[(E)-1,3-benzodioxol-5-ylmethyleneamino]-6-methyl-[1,3]dioxolo[4,5-g]quinolin-8-amine

Chemical Property:

Vapor Pressure:7.05E-12mmHg at 25°C
XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:3
Exact Mass:349.10625597
Heavy Atom Count:26
Complexity:533

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=C2C=C3C(=CC2=N1)OCO3)NN=CC4=CC5=C(C=C4)OCO5
Isomeric SMILES:CC1=CC(=C2C=C3C(=CC2=N1)OCO3)N/N=C/C4=CC5=C(C=C4)OCO5

Technology Process of N-[(E)-1,3-benzodioxol-5-ylmethyleneamino]-6-methyl-[1,3]dioxolo[4,5-g]quinolin-8-amine

There total 5 articles about N-[(E)-1,3-benzodioxol-5-ylmethyleneamino]-6-methyl-[1,3]dioxolo[4,5-g]quinolin-8-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:

: 14268-66-7
benzo[1,3]dioxolo-5-ylamine

: 91919-02-7
NSC332389

Guidance literature:: Multi-step reaction with 5 steps

1: 48 h / Heating

2: neat (no solvent) / 0.33 h

3: POCl₃ / neat (no solvent) / 1 h / 170 °C

4: hydrazine hydrate / ethanol / 24 h / Heating

5: ethanol / 2 h / Heating

With hydrazine hydrate; trichlorophosphate; In ethanol;

Reference yield:

: 91918-88-6
β-(3,4-metilendiossifenilammino)crotonato di etile

: 91919-02-7
NSC332389

Guidance literature:: Multi-step reaction with 4 steps

1: neat (no solvent) / 0.33 h

2: POCl₃ / neat (no solvent) / 1 h / 170 °C

3: hydrazine hydrate / ethanol / 24 h / Heating

4: ethanol / 2 h / Heating

With hydrazine hydrate; trichlorophosphate; In ethanol;

Reference yield:

: 50593-65-2
6-metil-8-cloro-1,3-diossol<4,5-g>chinolina

: 91919-02-7
NSC332389

Guidance literature:: Multi-step reaction with 2 steps

1: hydrazine hydrate / ethanol / 24 h / Heating

2: ethanol / 2 h / Heating

With hydrazine hydrate; In ethanol;