N-(4-Formylpyrimidin-2-yl)acetamide

Base Information

Chemical Name:N-(4-Formylpyrimidin-2-yl)acetamide
CAS No.:180869-44-7
Molecular Formula:C7H7N3O2
Molecular Weight:165.14938
Hs Code.:2933599090
DSSTox Substance ID:DTXSID801293688
Mol file:180869-44-7.mol

Synonyms:N-(4-Formylpyrimidin-2-yl)acetamide;180869-44-7;Acetamide, N-(4-formyl-2-pyrimidinyl)-;2-Acetamidopyrimidine-4-carboxaldehyde;SCHEMBL7091263;LZTGSSLTXVSGEW-UHFFFAOYSA-N;DTXSID801293688;N-(4-Formyl-2-pyrimidinyl)acetamide;SB56220;DA-43474;A853876

Suppliers and Price of N-(4-Formylpyrimidin-2-yl)acetamide

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-(4-Formylpyrimidin-2-yl)acetamide 95+%
1g
$ 672.00

Chemenu
N-(4-formylpyrimidin-2-yl)acetamide 95%
1g
$ 635.00

Total 8 raw suppliers

Chemical Property of N-(4-Formylpyrimidin-2-yl)acetamide

Chemical Property:

PSA：75.44000
LogP:0.89700
Storage Temp.:2-8°C
XLogP3:-0.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:165.053826475
Heavy Atom Count:12
Complexity:184

Purity/Quality:

97% ^*data from raw suppliers

N-(4-Formylpyrimidin-2-yl)acetamide 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=NC=CC(=N1)C=O

Technology Process of N-(4-Formylpyrimidin-2-yl)acetamide

There total 3 articles about N-(4-Formylpyrimidin-2-yl)acetamide 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:

: 2-acetamidopyrimidine-4-carboxaldehyde monomethyl monoacetoxy acetal

: 75-09-2
dichloromethane

: 180869-44-7
2-acetamidopyrimidine-4-carboxaldehyde

Guidance literature:: With hydrogenchloride; sodium methylate; In methanol;

Reference yield:

: 67751-23-9,187242-85-9
(E)-4-(dimethylamino)-1,1-dimethoxybut-3-en-2-one

: 180869-44-7
2-acetamidopyrimidine-4-carboxaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaOH

2: 2.) H₂SO₄, 3.) methanolic NaOH

With sodium hydroxide; sulfuric acid;
DOI:10.1016/S0960-894X(98)00549-6