N,N-Dibutylbenzamide

Base Information Edit

Chemical Name:N,N-Dibutylbenzamide
CAS No.:25033-65-2
Molecular Formula:C15H23 N O
Molecular Weight:233.354
Hs Code.:
European Community (EC) Number:811-334-9
NSC Number:73161
DSSTox Substance ID:DTXSID60179741
Nikkaji Number:J122.374G
Wikidata:Q83050264
Mol file:25033-65-2.mol

Synonyms:N,N-DIBUTYLBENZAMIDE;25033-65-2;Benzamide, N,N-dibutyl-;Di-N-n-butylbenzoic acid amide;NSC73161;Benzamide,N-dibutyl-;N,N-dibutyl-benzamide;CBMicro_009354;SCHEMBL1004032;DTXSID60179741;RYGJQVQEGCQNHM-UHFFFAOYSA-N;SMSF0005689;MFCD01010559;NSC 73161;NSC-73161;AKOS003283601;CB12469;BIM-0009555.P001;AG-690/11171139

Suppliers and Price of N,N-Dibutylbenzamide

Supply Marketing:Edit

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

Total 2 raw suppliers

Chemical Property of N,N-Dibutylbenzamide Edit

Chemical Property:

Vapor Pressure:4.11E-05mmHg at 25°C
Boiling Point:351.4°Cat760mmHg
Flash Point:151°C
PSA：20.31000
Density:0.957g/cm³
LogP:3.72900
XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:7
Exact Mass:233.177964357
Heavy Atom Count:17
Complexity:201

Purity/Quality:: 99%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCN(CCCC)C(=O)C1=CC=CC=C1

Technology Process of N,N-Dibutylbenzamide

There total 42 articles about N,N-Dibutylbenzamide 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: 99.0%

: 591-50-4
iodobenzene

: 201230-82-2
carbon monoxide

: 111-92-2
dibutylamine

: 25033-65-2
N,N-dibutylbenzamide

Guidance literature:: With dipotassium hydrogenphosphate; palladium; potassium iodide; In 1,4-dioxane; at 130 ℃; for 12h; under 3750.38 Torr; Autoclave; Green chemistry;
DOI:10.1039/c8gc00740c

Reference yield: 98.0%

: 999-33-7
N-chloro-N,N-dibutylamine

: 100-52-7
benzaldehyde

: 25033-65-2
N,N-dibutylbenzamide

Guidance literature:: With tert.-butylhydroperoxide; iron(III) chloride hexahydrate; In water; acetonitrile; Inert atmosphere; Reflux;
DOI:10.1002/adsc.201200659 DOI:10.1002/adsc.201200659

Reference yield: 93.0%

: 591-50-4
iodobenzene

: 102-82-9
tributyl-amine

: 201230-82-2
carbon monoxide

: 25033-65-2
N,N-dibutylbenzamide

Guidance literature:: With palladium 10% on activated carbon; oxygen; In acetonitrile; at 100 ℃; for 8h; under 4560.31 Torr; Autoclave; Green chemistry;
DOI:10.1021/acs.joc.5b02385