2,6-Dimethylcarbanilic acid 2-(1-pyrrolidinyl)cyclohexyl ester hydrochloride

Base Information

Chemical Name:2,6-Dimethylcarbanilic acid 2-(1-pyrrolidinyl)cyclohexyl ester hydrochloride
CAS No.:20131-73-1
Molecular Formula:C₁₉H₂₈N₂O₂*ClH
Molecular Weight:352.904
Hs Code.:

Synonyms:K 1502;2,6-Dimethylcarbanilic acid 2-(1-pyrrolidinyl)cyclohexyl ester hydrochloride;2-(1-Pyrrolidinyl)cyclohexyl 2,6-dimethylcarbanilate hydrochloride;Carbanilic acid, 2,6-dimethyl-, 2-(1-pyrrolidinyl)cyclohexyl ester, hydrochloride;20131-73-1;C19H28N2O2.ClH;LS-51195

Suppliers and Price of 2,6-Dimethylcarbanilic acid 2-(1-pyrrolidinyl)cyclohexyl ester hydrochloride

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 2,6-Dimethylcarbanilic acid 2-(1-pyrrolidinyl)cyclohexyl ester hydrochloride

Chemical Property:

Vapor Pressure:1.37E-06mmHg at 25°C
Boiling Point:399.5°Cat760mmHg
Flash Point:195.4°C
PSA：45.06000
Density:g/cm³
LogP:5.01240
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:352.1917559
Heavy Atom Count:24
Complexity:385

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C(=CC=C1)C)NC(=O)OC2CCCCC2[NH+]3CCCC3.[Cl-]

Technology Process of 2,6-Dimethylcarbanilic acid 2-(1-pyrrolidinyl)cyclohexyl ester hydrochloride

There total 1 articles about 2,6-Dimethylcarbanilic acid 2-(1-pyrrolidinyl)cyclohexyl ester hydrochloride 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: