Cycloheptanone, cycloheptylidenehydrazone

Base Information

Chemical Name:Cycloheptanone, cycloheptylidenehydrazone
CAS No.:24214-70-8
Molecular Formula:C14H24 N2
Molecular Weight:220.358
Hs Code.:
DSSTox Substance ID:DTXSID00178910
Nikkaji Number:J31.676H

Synonyms:Cycloheptanone, cycloheptylidenehydrazone;24214-70-8;SCHEMBL1255020;DTXSID00178910

Suppliers and Price of Cycloheptanone, cycloheptylidenehydrazone

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 Cycloheptanone, cycloheptylidenehydrazone

Chemical Property:

Vapor Pressure:0.000349mmHg at 25°C
Boiling Point:329°C at 760 mmHg
PKA:9.00±0.20(Predicted)
Flash Point:144.9°C
PSA：24.72000
Density:1.04g/cm³
LogP:4.49180
XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:220.193948774
Heavy Atom Count:16
Complexity:218

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCCC(=NN=C2CCCCCC2)CC1

Technology Process of Cycloheptanone, cycloheptylidenehydrazone

There total 4 articles about Cycloheptanone, cycloheptylidenehydrazone 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: 89.0%

: 502-41-0
cycloheptanol

: 24214-70-8
N,N'-dicycloheptylidenehydrazine

Guidance literature:: With [carbonylchlorohydrido{bis[2-(diphenylphosphinomethyl)ethyl]amino}ethylamino] ruthenium(II); potassium tert-butylate; hydrazine hydrate; In toluene; at 125 ℃; for 12h; Schlenk technique; Molecular sieve; Inert atmosphere; Green chemistry;
DOI:10.1039/c9cc01383k