N-butyl-3-chlorobenzamide

Base Information

Chemical Name:N-butyl-3-chlorobenzamide
CAS No.:35306-53-7
Molecular Formula:C₁₁H₁₄ClNO
Molecular Weight:211.691
Hs Code.:
European Community (EC) Number:657-604-8
Nikkaji Number:J1.583.768C
Mol file:35306-53-7.mol

Synonyms:N-butyl-3-chlorobenzamide;35306-53-7;N-n-Butyl-3-chlorobenzamide;Benzamide, 3-chloro-N-butyl-;SCHEMBL6358483;NKQOQWJDLCYELT-UHFFFAOYSA-N;STK416456;AKOS003277622;NCGC00328241-01;CS-0297692;AB01323677-02

Suppliers and Price of N-butyl-3-chlorobenzamide

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

Crysdot
N-Butyl-3-chlorobenzamide 95+%
5g
$ 1131.00

Crysdot
N-Butyl-3-chlorobenzamide 95+%
1g
$ 424.00

Aronis compounds
N-butyl-3-chlorobenzamide
50mg
$ 50.00

Aronis compounds
N-butyl-3-chlorobenzamide
5mg
$ 15.00

American Custom Chemicals Corporation
N-BUTYL-3-CHLOROBENZAMIDE 95.00%
5MG
$ 498.03

Total 5 raw suppliers

Chemical Property of N-butyl-3-chlorobenzamide

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:211.0763918
Heavy Atom Count:14
Complexity:184

Purity/Quality:

99% ^*data from raw suppliers

N-Butyl-3-chlorobenzamide 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCNC(=O)C1=CC(=CC=C1)Cl

Technology Process of N-butyl-3-chlorobenzamide

There total 8 articles about N-butyl-3-chlorobenzamide 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: 98.0%

: 201230-82-2
carbon monoxide

: 625-99-0
3-iodochlorobenzene

: 109-73-9,85404-21-3
N-butylamine

: 35306-53-7
N-butyl-3-chlorobenzamide

Guidance literature:: With palladium diacetate; potassium carbonate; In glycerol; at 60 ℃; for 12h; under 20521.4 Torr; Solvent; chemoselective reaction; Autoclave; Green chemistry;
DOI:10.1039/c8cc03858a

Reference yield: 77.0%

: 201230-82-2
carbon monoxide

: 625-99-0
3-iodochlorobenzene

: 109-73-9,85404-21-3
N-butylamine

: 35306-53-7
N-butyl-3-chlorobenzamide

: N-butyl-3-chlorophenylglyoxamide

Guidance literature:: With 1,4-diaza-bicyclo[2.2.2]octane; bis(η3-allyl-μ-chloropalladium(II)); triphenylphosphine; In tetrahydrofuran; at 25 ℃; for 12h; under 760.051 Torr;
DOI:10.1021/jo0156924

Reference yield: 69.0%

: 108-41-8
1-chloro-3-methylbenzene

: 109-73-9,85404-21-3
N-butylamine

: 35306-53-7
N-butyl-3-chlorobenzamide

Guidance literature:: With tert.-butylhydroperoxide; iron(III) chloride hexahydrate; tetra-(n-butyl)ammonium iodide; In water; at 60 ℃; for 24h; Molecular sieve; Sealed tube; Green chemistry;
DOI:10.1039/c5gc00299k