N-(4-Methoxybenzyl)Acetoacetamide

Base Information

Chemical Name:N-(4-Methoxybenzyl)Acetoacetamide
CAS No.:51719-12-1
Molecular Formula:C12H15NO3
Molecular Weight:221.256
Hs Code.:2924299090
NSC Number:96631
DSSTox Substance ID:DTXSID70966003
Nikkaji Number:J3.112.095K
Wikidata:Q82948336
Mol file:51719-12-1.mol

Synonyms:N-(4-Methoxybenzyl)Acetoacetamide;51719-12-1;N-[(4-methoxyphenyl)methyl]-3-oxobutanamide;NSC96631;SCHEMBL5902331;DTXSID70966003;NSC-96631;AKOS000165467;FT-0700322;SR-01000203235;J-690312;N-[(4-Methoxyphenyl)methyl]-3-oxobutanimidic acid;SR-01000203235-1

Suppliers and Price of N-(4-Methoxybenzyl)Acetoacetamide

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-(4-Methoxybenzyl)acetoacetamide
250mg
$ 65.00

Sigma-Aldrich
N-(4-METHOXYBENZYL)ACETOACETAMIDE Aldrich
1g
$ 144.00

American Custom Chemicals Corporation
N-(4-METHOXYBENZYL)ACETOACETAMIDE 95.00%
1G
$ 712.41

Total 7 raw suppliers

Chemical Property of N-(4-Methoxybenzyl)Acetoacetamide

Chemical Property:

Vapor Pressure:8.09E-08mmHg at 25°C
Boiling Point:436.4°Cat760mmHg
Flash Point:217.7°C
PSA：55.40000
Density:1.112g/cm³
LogP:1.68140
XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:221.10519334
Heavy Atom Count:16
Complexity:245

Purity/Quality:

99% ^*data from raw suppliers

N-(4-Methoxybenzyl)acetoacetamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)CC(=O)NCC1=CC=C(C=C1)OC

Technology Process of N-(4-Methoxybenzyl)Acetoacetamide

There total 2 articles about N-(4-Methoxybenzyl)Acetoacetamide 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: 77.0%

: 674-82-8,2130-41-8
4-methyleneoxetan-2-one

: 2393-23-9
4-methoxy-benzylamine

: 51719-12-1
N-(4-methoxybenzyl)-3-oxobutanamide

Guidance literature:: In methanol; at 0 ℃; Inert atmosphere;
DOI:10.1016/j.bmc.2010.02.024

Reference yield:

: 85920-63-4
5-(1-hydroxyethylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione

: 2393-23-9
4-methoxy-benzylamine

: 51719-12-1
N-(4-methoxybenzyl)-3-oxobutanamide

Guidance literature:: In toluene; for 1h; Heating;
DOI:10.1002/ejoc.200390091

Reference yield: 92.0%

: 51719-12-1
N-(4-methoxybenzyl)-3-oxobutanamide

: 1439365-79-3
2,2-difluoro-N-(4-methoxybenzyl)-3-oxobutanamide

Guidance literature:: With 1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2 2 2]octane bis(tetrafluoroborate); potassium carbonate; In water; at 20 ℃; for 16h;
DOI:10.1016/j.jfluchem.2013.03.016