n-Ethyl-3-hydroxynaphthalene-2-carboxamide

Base Information

Chemical Name:n-Ethyl-3-hydroxynaphthalene-2-carboxamide
CAS No.:5272-85-5
Molecular Formula:C15H13N3
Molecular Weight:235.288
Hs Code.:
NSC Number:37091
DSSTox Substance ID:DTXSID00967169
Mol file:5272-85-5.mol

Synonyms:6272-12-4;n-ethyl-3-hydroxynaphthalene-2-carboxamide;NSC37091;SCHEMBL9313734;DTXSID00967169;NSC-37091;AKOS008919962;N-Ethyl-3-hydroxynaphthalene-2-carboximidic acid;Z30281220

Suppliers and Price of n-Ethyl-3-hydroxynaphthalene-2-carboxamide

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

Crysdot
3,5-Diphenyl-1H-pyrazol-4-amine 95+%
1g
$ 668.00

Chemenu
3,5-diphenyl-1H-pyrazol-4-amine 95%
1g
$ 631.00

American Custom Chemicals Corporation
3,5-DIPHENYL-1H-PYRAZOL-4-AMINE 95.00%
5MG
$ 502.35

Total 7 raw suppliers

Chemical Property of n-Ethyl-3-hydroxynaphthalene-2-carboxamide

Chemical Property:

Vapor Pressure:1.54E-08mmHg at 25°C
PSA：54.70000
LogP:3.90710
Storage Temp.:2-8°C
XLogP3:3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:215.094628657
Heavy Atom Count:16
Complexity:254

Purity/Quality:

97% ^*data from raw suppliers

3,5-Diphenyl-1H-pyrazol-4-amine 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCNC(=O)C1=CC2=CC=CC=C2C=C1O

Technology Process of n-Ethyl-3-hydroxynaphthalene-2-carboxamide

There total 5 articles about n-Ethyl-3-hydroxynaphthalene-2-carboxamide 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:

: 40697-59-4
benzylidene-(3,5-diphenyl-1H-pyrazol-4-yl)-amine

: 5272-85-5
4-amino-3,5-diphenylpyrazole

: 100-52-7
benzaldehyde

Guidance literature:: With hydrogenchloride; potassium carbonate; Yield given. Multistep reaction; 1) heating;

Reference yield:

: 942228-01-5
4-amino-3,5-diphenylisothiazole

: 5272-85-5
4-amino-3,5-diphenylpyrazole

Guidance literature:: With hydrazine; at 150 ℃; for 480h;
DOI:10.1016/j.tet.2009.06.041

Reference yield:

: 6830-78-0
3,6-diphenyl-1,2,4,5-tetrazine

: 5272-85-5
4-amino-3,5-diphenylpyrazole

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / CH₂Cl₂ / 0 °C

2: 1) conc. HCl, 2) aq. K₂CO₃ / 1) heating

With hydrogenchloride; potassium carbonate; In dichloromethane;