Carbamic acid, (5-((cyclohexylamino)acetyl)-10,11-dihydro-5H-dibenz(b,f)azepin-3-yl)-, ethyl ester, hydrochloride, hydrate (1:1:1)

Base Information

Chemical Name:Carbamic acid, (5-((cyclohexylamino)acetyl)-10,11-dihydro-5H-dibenz(b,f)azepin-3-yl)-, ethyl ester, hydrochloride, hydrate (1:1:1)
CAS No.:134068-39-6
Molecular Formula:C25H32ClN3O3
Molecular Weight:457.9929
Hs Code.:
DSSTox Substance ID:DTXSID20158491

Synonyms:3-Carbethoxyamino-5-cyclohexylaminoacetyl-10,11-dihydro-5H-dibenz(b,f)azepine hydrochloride;134068-39-6;Ethyl (5-((cyclohexylamino)acetyl)-10,11-dihydro-5H-dibenz(b,f)azepin-3-yl)carbamate HCl H2O;Carbamic acid, (5-((cyclohexylamino)acetyl)-10,11-dihydro-5H-dibenz(b,f)azepin-3-yl)-, ethyl ester, hydrochloride, hydrate (1:1:1);ethyl N-[11-[2-(cyclohexylamino)acetyl]-5,6-dihydrobenzo[b][1]benzazepin-2-yl]carbamate;hydrochloride;C25H31N3O3.ClH.H2O;DTXSID20158491;C25-H31-N3-O3.Cl-H.H2-O;LS-49202

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Carbamic acid, (5-((cyclohexylamino)acetyl)-10,11-dihydro-5H-dibenz(b,f)azepin-3-yl)-, ethyl ester, hydrochloride, hydrate (1:1:1)

Chemical Property:

Vapor Pressure:2.86E-14mmHg at 25°C
Boiling Point:598.1°Cat760mmHg
Flash Point:315.5°C
Density:g/cm³
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:457.2132196
Heavy Atom Count:32
Complexity:607

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)NC1=CC2=C(CCC3=CC=CC=C3N2C(=O)CNC4CCCCC4)C=C1.Cl

Technology Process of Carbamic acid, (5-((cyclohexylamino)acetyl)-10,11-dihydro-5H-dibenz(b,f)azepin-3-yl)-, ethyl ester, hydrochloride, hydrate (1:1:1)

There total 1 articles about Carbamic acid, (5-((cyclohexylamino)acetyl)-10,11-dihydro-5H-dibenz(b,f)azepin-3-yl)-, ethyl ester, hydrochloride, hydrate (1:1:1) 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: 56.7%