30668-14-5 Usage
Description
1-Morpholinopropan-1-one, also known as MPO, is a chemical compound with the molecular formula C7H13NO2. It is a versatile intermediate used in the production of various compounds such as pharmaceuticals, agrochemicals, and other organic synthesis.
Used in Pharmaceutical Industry:
1-Morpholinopropan-1-one is used as a building block for the synthesis of heterocyclic compounds, which are important in the development of pharmaceuticals.
Used in Agrochemical Industry:
1-Morpholinopropan-1-one is used as an intermediate in the production of agrochemicals, contributing to the development of effective crop protection products.
Used in Chemical Research:
1-Morpholinopropan-1-one is used as a solvent in various chemical reactions, facilitating the synthesis of new compounds and aiding in research and development.
Used in Polymer Production:
1-Morpholinopropan-1-one is used as a reagent in the production of polymers, playing a role in the creation of a wide range of polymeric materials.
Used in Organic Chemistry:
1-Morpholinopropan-1-one is used as a reagent in organic chemistry, enabling the synthesis of various organic compounds and contributing to the advancement of the field.
Check Digit Verification of cas no
The CAS Registry Mumber 30668-14-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,6 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 30668-14:
(7*3)+(6*0)+(5*6)+(4*6)+(3*8)+(2*1)+(1*4)=105
105 % 10 = 5
So 30668-14-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO2/c1-2-7(9)8-3-5-10-6-4-8/h2-6H2,1H3
30668-14-5Relevant articles and documents
Catalytic α-Hydroarylation of Acrylates and Acrylamides via an Interrupted Hydrodehalogenation Reaction
Cherney, Emily C.,Engle, Keary M.,Gurak, John A.,Joe, Candice L.,Vasquez, Alena M.
supporting information, p. 10477 - 10484 (2020/08/07)
The palladium-catalyzed, α-selective hydroarylation of acrylates and acrylamides is reported. Under optimized conditions, this method is highly tolerant of a wide range of substrates including those with base sensitive functional groups and/or multiple enolizable carbonyl groups. A detailed mechanistic study was undertaken, and the high selectivity of this transformation was shown to be enabled by the formation of a [PdII(Ar)(H)] intermediate, which performs selective hydride insertion into the β-position of α,β-unsaturated carbonyl compounds.
Selective catalytic sp3 C-O bond cleavage with C-N bond formation in 3-alkoxy-1-propanols
Chen, Cheng,Hong, Soon Hyeok
supporting information; experimental part, p. 2992 - 2995 (2012/07/28)
The ruthenium catalyzed selective sp3 C-O cleavage with amide formation was reported in reactions of 3-alkoxy-1-propanol derivatives and amines. The cleavage only occurs at the C3-O position even with 3-benzyloxy-1-propanol. Based on the experimental results, O-bound and C-bound Ru enolate complexes were proposed as key intermediates for the unique selective sp3 C-O bond cleavage in 3-alkoxy-1-propanols.