2-((4-methoxynaphthalen-2-yl)amino)-5-nitrobenzoic acid

Base Information

Chemical Name:2-((4-methoxynaphthalen-2-yl)amino)-5-nitrobenzoic acid
CAS No.:1572936-83-4
Molecular Formula:C₁₈H₁₄N₂O₅
Molecular Weight:338.32
Hs Code.:
Mol file:1572936-83-4.mol

Synonyms:2-[(4-methoxy-2-naphthalenyl)amino]-5-nitro-benzoic acid

Suppliers and Price of 2-((4-methoxynaphthalen-2-yl)amino)-5-nitrobenzoic acid

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

TRC
2-[(4-Methoxy-2-naphthalenyl)amino]-5-nitrobenzoicAcid
5mg
$ 85.00

Cayman Chemical
MONNA ≥98%
1mg
$ 25.00

Cayman Chemical
MONNA ≥98%
10mg
$ 138.00

Cayman Chemical
MONNA ≥98%
5mg
$ 94.00

Cayman Chemical
MONNA ≥98%
25mg
$ 313.00

AK Scientific
Monna
10mg
$ 286.00

AK Scientific
Monna
1mg
$ 133.00

Total 9 raw suppliers

Chemical Property of 2-((4-methoxynaphthalen-2-yl)amino)-5-nitrobenzoic acid

Chemical Property:

Purity/Quality:

97% ^*data from raw suppliers

2-[(4-Methoxy-2-naphthalenyl)amino]-5-nitrobenzoicAcid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Description MONNA is a selective inhibitor of anoctamin-1 (ANO1; IC50 = 0.08 μM in Xenopus oocytes), a calcium-activated chloride channel (CaCC). It is selective for ANO1 over the chloride channels bestrophin-1, chloride channel protein 2, and cystic fibrosis transmembrane conductance regulator up to 10 μM. MONNA (10 μM) induces full vasorelaxation of preconstricted mouse isolated mesenteric arteries in the presence or absence of chloride. It also hyperpolarizes isolated rat mesenteric arteries under resting conditions.
Uses 2-[(4-Methoxy-2-naphthalenyl)amino]-5-nitrobenzoic Acid selectively inhibits the calcium-activated chloride channel, anoctamin-1. 2-[(4-Methoxy-2-naphthalenyl)amino]-5-nitrobenzoic Acid has potential applications for developing treatments for hypertension, cystic fibrosis, bronchitis, asthma, and hyperalgesia.

Technology Process of 2-((4-methoxynaphthalen-2-yl)amino)-5-nitrobenzoic acid

There total 2 articles about 2-((4-methoxynaphthalen-2-yl)amino)-5-nitrobenzoic acid 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: 98.0%