Semicarbazide, 1,4-dibenzoyl-

Base Information

Chemical Name:Semicarbazide, 1,4-dibenzoyl-
CAS No.:16956-44-8
Molecular Formula:C15H13 N3 O3
Molecular Weight:283.287
Hs Code.:2928000090
DSSTox Substance ID:DTXSID70168722
Nikkaji Number:J62.774G
Wikidata:Q83038347
Mol file:16956-44-8.mol

Synonyms:1,4-Dibenzoylsemicarbazide;SEMICARBAZIDE, 1,4-DIBENZOYL-;16956-44-8;BRN 2595295;N-(benzamidocarbamoyl)benzamide;Benzoic acid, 2-[(benzoylamino)carbonyl]hydrazide;4-09-00-00936 (Beilstein Handbook Reference);C15H13N3O3;DTXSID70168722;NHXXLEBCTOQKJS-UHFFFAOYSA-N;N,2-Dibenzoylhydrazinecarboxamide #;LS-144875

Suppliers and Price of Semicarbazide, 1,4-dibenzoyl-

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
1,4-DIBENZOYLSEMICARBAZIDE 95.00%
5MG
$ 505.73

Total 2 raw suppliers

Chemical Property of Semicarbazide, 1,4-dibenzoyl-

Chemical Property:

Melting Point:186-187 °C
PKA:9.07±0.43(Predicted)
PSA：97.77000
Density:1.284g/cm³
LogP:2.82500
XLogP3:2.5
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:283.09569129
Heavy Atom Count:21
Complexity:386

Purity/Quality:

99% ^*data from raw suppliers

1,4-DIBENZOYLSEMICARBAZIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)NC(=O)NNC(=O)C2=CC=CC=C2

Technology Process of Semicarbazide, 1,4-dibenzoyl-

There total 3 articles about Semicarbazide, 1,4-dibenzoyl- 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:

: 613-94-5
benzoic acid hydrazide

: 4461-33-0
benzoyl isocyanate

: 16956-44-8
N,2-dibenzoylhydrazine-1-carboxamide

Guidance literature:: In toluene; Schlenk technique; Inert atmosphere; Reflux;
DOI:10.1055/s-0036-1588724

Reference yield:

: C₉H₇ClN₂O₃

: 55-21-0,27208-38-4
benzamide

: 35658-16-3
Oxalsaeure-bis-<β-benzoylhydrazid>

: 16956-44-8
N,2-dibenzoylhydrazine-1-carboxamide

Guidance literature:: In toluene; Schlenk technique; Inert atmosphere; Reflux;
DOI:10.1055/s-0036-1588724

Reference yield:

: 55-21-0,27208-38-4
benzamide

: 16956-44-8
N,2-dibenzoylhydrazine-1-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / Inert atmosphere; Schlenk technique; Reflux

2: toluene / Schlenk technique; Inert atmosphere; Reflux

In dichloromethane; toluene;
DOI:10.1055/s-0036-1588724