N-methoxy-N-methylpentanamide

Base Information

Chemical Name:N-methoxy-N-methylpentanamide
CAS No.:129118-11-2
Molecular Formula:C7H15NO2
Molecular Weight:145.202
Hs Code.:2924199090
DSSTox Substance ID:DTXSID70396624
Nikkaji Number:J314.502F
Wikidata:Q82197425
Mol file:129118-11-2.mol

Synonyms:N-methoxy-N-methylpentanamide;129118-11-2;N-methoxy-N-methylvaleramide;SCHEMBL211903;DTXSID70396624;CDTCEEGTCPVQNX-UHFFFAOYSA-N;Pentanamide, N-methoxy-N-methyl-;butyl-n-methoxy-n-methylcarboxamide;pentanoic acid methoxy-methyl-amide;MFCD05149014;AKOS008952714;AM90039;BS-20631;N-Methylvalerohydroxamic acid methyl ester;CS-0123008;FT-0749340;E77912;A849004

Suppliers and Price of N-methoxy-N-methylpentanamide

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

TRC
N-Methoxy-N-methylpentanamide
500mg
$ 70.00

Crysdot
N-Methoxy-N-methylpentanamide 95+%
25g
$ 549.00

American Custom Chemicals Corporation
N-METHOXY-N-METHYLPENTANAMIDE 95.00%
5MG
$ 496.80

AK Scientific
N-Methoxy-N-methylpentanamide
5g
$ 291.00

aablocks
N-Methoxy-N-methylpentanamide 95%
1g
$ 60.00

Total 5 raw suppliers

Chemical Property of N-methoxy-N-methylpentanamide

Chemical Property:

PSA：29.54000
LogP:1.19640
XLogP3:1.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:145.110278721
Heavy Atom Count:10
Complexity:104

Purity/Quality:

97% ^*data from raw suppliers

N-Methoxy-N-methylpentanamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCC(=O)N(C)OC

Technology Process of N-methoxy-N-methylpentanamide

There total 7 articles about N-methoxy-N-methylpentanamide 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: 93.0%

: 6638-79-5
N,O-dimethylhydroxylamine*hydrochloride

: 638-29-9
n-valeryl chloride

: 129118-11-2
N-methoxy-N-methyl-n-pentanamide

Guidance literature:: With potassium carbonate; In 2-methyltetrahydrofuran; water; at 0 - 20 ℃;
DOI:10.1039/c3ra41262h

Reference yield: 89.0%

: 109-72-8,29786-93-4
n-butyllithium

: 123707-26-6
N,N'-dimethoxy-N,N'-dimethyl urea

: 129118-11-2
N-methoxy-N-methyl-n-pentanamide

Guidance literature:: In tetrahydrofuran; at 22 ℃;
DOI:10.1021/jo00008a057

Reference yield: 85.0%

: 6638-79-5
N,O-dimethylhydroxylamine*hydrochloride

: 109-52-4
valeric acid

: 129118-11-2
N-methoxy-N-methyl-n-pentanamide

Guidance literature:: With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃; for 20h;