Benzamide, N-[(hexahydro-1H-azepin-1-yl)thioxomethyl]-4-methoxy-

Base Information

Chemical Name:Benzamide, N-[(hexahydro-1H-azepin-1-yl)thioxomethyl]-4-methoxy-
CAS No.:114171-16-3
Molecular Formula:C15H20N2O2S
Molecular Weight:292.39700
Hs Code.:
DSSTox Substance ID:DTXSID90356442
Wikidata:Q82135773
Mol file:114171-16-3.mol

Synonyms:114171-16-3;N-(azepane-1-carbothioyl)-4-methoxybenzamide;Benzamide, N-[(hexahydro-1H-azepin-1-yl)thioxomethyl]-4-methoxy-;CBMicro_025197;Oprea1_287025;DTXSID90356442;CCG-12252;AKOS003422227;BIM-0025178.P001;N-(1-azepanylcarbothioyl)-4-methoxybenzamide;AB-601/30968052;SR-01000214181;SR-01000214181-1;N~1~-(1-AZEPANYLCARBOTHIOYL)-4-METHOXYBENZAMIDE

Suppliers and Price of Benzamide, N-[(hexahydro-1H-azepin-1-yl)thioxomethyl]-4-methoxy-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of Benzamide, N-[(hexahydro-1H-azepin-1-yl)thioxomethyl]-4-methoxy-

Chemical Property:

PSA：77.15000
LogP:3.09860
XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:292.12454906
Heavy Atom Count:20
Complexity:333

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)C(=O)NC(=S)N2CCCCCC2

Technology Process of Benzamide, N-[(hexahydro-1H-azepin-1-yl)thioxomethyl]-4-methoxy-

There total 3 articles about Benzamide, N-[(hexahydro-1H-azepin-1-yl)thioxomethyl]-4-methoxy- 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: 82.0%