p-Octyloxybenzaldehyde 3-thiosemicarbazone

Base Information

Chemical Name:p-Octyloxybenzaldehyde 3-thiosemicarbazone
CAS No.:73962-30-8
Molecular Formula:C₁₆H₂₅N₃OS
Molecular Weight:307.46
Hs Code.:
Mol file:73962-30-8.mol

Synonyms:p-Octyloxybenzaldehyde 3-thiosemicarbazone;73962-30-8;[(E)-(4-octoxyphenyl)methylideneamino]thiourea;BRN 3358334;BENZALDEHYDE, p-OCTYLOXY-, 3-THIOSEMICARBAZONE;(e)-4-octyloxybenzaldehyde thiosemicarbazone;4-08-00-00285 (Beilstein Handbook Reference);C16H25N3OS;C16-H25-N3-O-S;STK949099;AKOS002183997;LS-25135;(2E)-2-[4-(octyloxy)benzylidene]hydrazinecarbothioamide

Suppliers and Price of p-Octyloxybenzaldehyde 3-thiosemicarbazone

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

American Custom Chemicals Corporation
PARA-OCTYLOXYBENZALDEHYDE-3-THIOSEMICARBAZONE 95.00%
5MG
$ 495.69

Total 3 raw suppliers

Chemical Property of p-Octyloxybenzaldehyde 3-thiosemicarbazone

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Melting Point:107.5-109.0 °C
Boiling Point:442.3°Cat760mmHg
PKA:11.35±0.70(Predicted)
Flash Point:221.3°C
Density:1.08g/cm³
XLogP3:4.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:10
Exact Mass:307.17183360
Heavy Atom Count:21
Complexity:302

Purity/Quality:

99% ^*data from raw suppliers

PARA-OCTYLOXYBENZALDEHYDE-3-THIOSEMICARBAZONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCOC1=CC=C(C=C1)C=NNC(=S)N
Isomeric SMILES:CCCCCCCCOC1=CC=C(C=C1)/C=N/NC(=S)N

Technology Process of p-Octyloxybenzaldehyde 3-thiosemicarbazone

There total 4 articles about p-Octyloxybenzaldehyde 3-thiosemicarbazone 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:

: 24083-13-4
4-octyloxybenzaldehyde

: 79-19-6
thiosemicarbazide

: 73962-30-8
4-octyloxy-benzaldehyde-thiosemicarbazone

Guidance literature:: acetic acid; In ethanol; for 0.25h; Heating;

Reference yield:

: 24083-13-4
4-octyloxybenzaldehyde

: 79-19-6
thiosemicarbazide

: 73962-30-8
C₁₆H₂₅N₃OS

Guidance literature:: In ethanol; Heating;
DOI:10.1080/10587250008025240

Reference yield:

: 111-83-1
1-bromo-octane

: 73962-30-8
C₁₆H₂₅N₃OS

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃ / cyclohexanone

2: aq. ethanol / Heating

With potassium carbonate; In ethanol; cyclohexanone;
DOI:10.1080/10587250008025240