Lactamide

Base Information

Chemical Name:Lactamide
CAS No.:2043-43-8
Molecular Formula:C3H7NO2
Molecular Weight:89.0941
Hs Code.:2924199090
European Community (EC) Number:218-049-3
NSC Number:61454,9903
UNII:4JZP7XJN3O
DSSTox Substance ID:DTXSID90862816
Nikkaji Number:J1.792B
Wikipedia:Lactamide
Wikidata:Q6468911
Metabolomics Workbench ID:71595
Mol file:2043-43-8.mol

Synonyms:lactamide

Suppliers and Price of Lactamide

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

Total 19 raw suppliers

Chemical Property of Lactamide

Chemical Property:

Vapor Pressure:0.000409mmHg at 25°C
Melting Point:73-76 °C
Refractive Index:1.459
Boiling Point:281.9 °C at 760 mmHg
PKA:13.34±0.20(Predicted)
Flash Point:124.3 °C
PSA：63.32000
Density:1.161 g/cm³
LogP:-0.44720
XLogP3:-1.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:89.047678466
Heavy Atom Count:6
Complexity:61.8

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C(=O)N)O

Technology Process of Lactamide

There total 26 articles about Lactamide 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%

: 78-97-7
2-hydroxy-propionitrile

: 598-81-2,2043-43-8,65144-02-7,89673-71-2
(+/-)-lactamide

Guidance literature:: With silver trifluoromethanesulfonate; C₃₃H₃₃ClO₇P₃Pt⁽¹⁺⁾*CF₃O₃S^(1-); In tetrahydrofuran; water; at 40 ℃; Catalytic behavior;
DOI:10.1021/acscatal.1c02254