Unii-xnv0707AMP

Base Information

Chemical Name:Unii-xnv0707AMP
CAS No.:492472-30-7
Molecular Formula:C₁₉H₂₂N₄O₂
Molecular Weight:338.409
Hs Code.:
UNII:XNV0707AMP
DSSTox Substance ID:DTXSID20197744
Nikkaji Number:J2.664.007E
Wikidata:Q27293919
ChEMBL ID:CHEMBL9676
Mol file:492472-30-7.mol

Synonyms:N-(2-(dimethylamino)ethyl)-2,6-dimethyl-1-oxo-1,2-dihydroxybenzo(b)-1,6-naphthyridine-4-carboxamide;SN 28049;SN-28049;SN28049

Suppliers and Price of Unii-xnv0707AMP

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 Unii-xnv0707AMP

Chemical Property:

PSA：70.72000
LogP:2.26130
XLogP3:1.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:338.17427596
Heavy Atom Count:25
Complexity:560

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C2C(=CC=C1)C=C3C(=N2)C(=CN(C3=O)C)C(=O)NCCN(C)C

Technology Process of Unii-xnv0707AMP

There total 5 articles about Unii-xnv0707AMP 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: 95.0%

: 108-00-9
N,N-dimethylethylenediamine

: 399017-31-3
2,6-dimethyl-1-oxo-1,2-dihydrobenzo[b][1,6]naphthyridine-4-carboxylic acid

: 492472-30-7
SN 28049

Guidance literature:: With thionyl chloride; In dichloromethane; at 20 ℃; for 16h; Heating / reflux;

Reference yield:

: 399017-29-9
ethyl (3-carboxy-8-methylquinolin-2-yl)acetate

: 492472-30-7
SN 28049

Guidance literature:: Multi-step reaction with 4 steps

1.1: phosphoryl chloride / 0.33 h / 0 °C

1.2: 97 percent / 1.5 h / 20 °C

2.1: 79 percent / tetrahydrofuran; dimethylformamide / 16 h / 20 °C

3.1: SOCl₂ / 0.5 h / Heating

4.1: 0.48 g / CH₂Cl₂ / 16 h / 20 °C

With thionyl chloride; trichlorophosphate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm020420u

Reference yield:

: 399017-31-3
2,6-dimethyl-1-oxo-1,2-dihydrobenzo[b][1,6]naphthyridine-4-carboxylic acid

: 492472-30-7
SN 28049

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂ / 0.5 h / Heating

2: 0.48 g / CH₂Cl₂ / 16 h / 20 °C

With thionyl chloride; In dichloromethane;
DOI:10.1021/jm020420u