Butanamide, 3-hydroxy-N,N-dimethyl-, (R)-

Base Information

Chemical Name:Butanamide, 3-hydroxy-N,N-dimethyl-, (R)-
CAS No.:89209-16-5
Molecular Formula:C₆H₁₃NO₂
Molecular Weight:131.175
Hs Code.:
European Community (EC) Number:829-102-0
Wikidata:Q76421834

Synonyms:Butanamide, 3-hydroxy-N,N-dimethyl-, (R)-;89209-16-5;(3R)-3-hydroxy-N,N-dimethylbutanamide;SCHEMBL3907850;EN300-6482740

Suppliers and Price of Butanamide, 3-hydroxy-N,N-dimethyl-, (R)-

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 3 raw suppliers

Chemical Property of Butanamide, 3-hydroxy-N,N-dimethyl-, (R)-

Chemical Property:

XLogP3:-0.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:131.094628657
Heavy Atom Count:9
Complexity:101

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(CC(=O)N(C)C)O
Isomeric SMILES:C[C@H](CC(=O)N(C)C)O

Technology Process of Butanamide, 3-hydroxy-N,N-dimethyl-, (R)-

There total 1 articles about Butanamide, 3-hydroxy-N,N-dimethyl-, (R)- 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:

: 57270-73-2
3-hydroxy-N,N-dimethylbutanamide

: 98-88-4
benzoyl chloride

: C₁₃H₁₇NO₃

: 1018832-70-6
C₁₃H₁₇NO₃

: 89209-16-5
(R)-3-hydroxy-N,N-dimethylbutanamide

: 89209-12-1
(S)-3-hydroxy-N,N-dimethylbutyramide

Guidance literature:: With potassium carbonate; copper(II) bis(trifluoromethanesulfonate); (4R,4'R)-2,2'-(propane-2,2'diyl)bis(4-phenyl-4,5-dihydrooxazole); In ethyl acetate; at 20 ℃; for 3h; Title compound not separated from byproducts.;
DOI:10.1055/s-2008-1032057