N,3,4,5-tetramethoxy-N-methylbenzamide

Base Information

Chemical Name:N,3,4,5-tetramethoxy-N-methylbenzamide
CAS No.:118779-14-9
Molecular Formula:C12H17NO5
Molecular Weight:255.271
Hs Code.:2924299090
European Community (EC) Number:696-553-6
NSC Number:106876
DSSTox Substance ID:DTXSID30296010
Wikidata:Q82036304
Mol file:118779-14-9.mol

Synonyms:N,3,4,5-tetramethoxy-N-methylbenzamide;118779-14-9;N,3,4,5-Tetramethoxy-N-methyl-benzamide;NSC106876;SCHEMBL709048;DTXSID30296010;DJECVTFEJVBYHR-UHFFFAOYSA-N;MFCD11718188;AKOS006037211;NSC-106876;C77791;CON(C)C(=O)C1=CC(OC)=C(OC)C(OC)=C1;N-methoxy-N-methyl-(3,4,5-trimethoxy)benzamide;Z28074734

Suppliers and Price of N,3,4,5-tetramethoxy-N-methylbenzamide

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,3,4,5-Tetramethoxy-N-methylbenzamide 95+%
5g
$ 589.00

Chemenu
N,3,4,5-Tetramethoxy-N-methylbenzamide 95%
5g
$ 556.00

American Custom Chemicals Corporation
N,3,4,5-TETRAMETHOXY-N-METHYLBENZAMIDE 95.00%
5MG
$ 502.40

Alichem
N,3,4,5-Tetramethoxy-N-methylbenzamide
5g
$ 630.70

Acrotein
N,3,4,5-Tetramethoxy-N-methyl-benzamide 97%
5g
$ 302.50

Total 6 raw suppliers

Chemical Property of N,3,4,5-tetramethoxy-N-methylbenzamide

Chemical Property:

PSA：57.23000
LogP:1.34580
Storage Temp.:2-8°C
XLogP3:1.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:255.11067264
Heavy Atom Count:18
Complexity:259

Purity/Quality:

99% ^*data from raw suppliers

N,3,4,5-Tetramethoxy-N-methylbenzamide 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C(=O)C1=CC(=C(C(=C1)OC)OC)OC)OC

Technology Process of N,3,4,5-tetramethoxy-N-methylbenzamide

There total 10 articles about N,3,4,5-tetramethoxy-N-methylbenzamide 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%

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

: 118-41-2
Eudesmic acid

: 118779-14-9
N-methoxy-N-methyl-3,4,5-trimethoxybenzamide

Guidance literature:: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; at 0 ℃; Inert atmosphere;
DOI:10.1021/ol101639g

Reference yield: 95.0%

: 201230-82-2
carbon monoxide

: 2675-79-8
1-bromo-3,4,5-trimethoxybenzene

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

: 118779-14-9
N-methoxy-N-methyl-3,4,5-trimethoxybenzamide

Guidance literature:: With potassium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In toluene; at 105 ℃; for 12h; under 2250.23 Torr; Inert atmosphere; Green chemistry;
DOI:10.1039/c4ra04614e

Reference yield: 91.0%

: 25245-29-8
5-iodo-1,2,3-trimethoxybenzene

: 201230-82-2
carbon monoxide

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

: 118779-14-9
N-methoxy-N-methyl-3,4,5-trimethoxybenzamide

Guidance literature:: With potassium carbonate; In toluene; at 105 ℃; for 12h; under 2250.23 Torr; Inert atmosphere; Green chemistry;
DOI:10.1039/c4ra04614e